- Research article
- Open Access
Social relationships, mental health and wellbeing in physical disability: a systematic review
BMC Public Health volume 17, Article number: 414 (2017)
- The Erratum to this article has been published in BMC Public Health 2017 17:580
Research has consistently found that favourable exchange with one’s proximal social environment has positive effects on both mental health and wellbeing. Adults with physical disabilities may have fewer opportunities of favourable exchange, and therefore the effects on mental health and wellbeing may be less advantageous. The aim of this study is to systematically review quantitative studies exploring associations of social relationships with mental health and wellbeing in persons with physical disabilities.
The databases PubMed, PsycINFO and Scopus were searched for relevant studies published between 1995 and 2016. Data was extracted on study and participants’ characteristics, independent and dependent variables, used measures and effects sizes of associations between social relationships and mental health or wellbeing. A narrative review was performed to synthesize findings along the constructs social support, social networks, negative social interactions, family functioning and relationship quality.
Of the 63 included studies, 47 were cross-sectional and 16 longitudinal. Most studies included a measure of social support (n = 58), while other concepts were less often studied (social networks n = 6; negative social interaction n = 3; family functioning n = 2; relationship quality n = 1). Over half of studies included depression as outcome (n = 33), followed by wellbeing (n = 14), composite mental health measures (n = 10), anxiety (n = 8), psychological distress (n = 7), posttraumatic stress disorder (n = 3), and hopelessness (n = 1). Although trends for associations of social support with mental health and wellbeing were consistent, around a quarter of studies failed to report significant associations. Social networks were related to depression, but not to other mental health or wellbeing measures. Family functioning, negative social interactions and relationship quality showed consistent associations with mental health and wellbeing, however, only few studies were available.
This review indicates that social relationships play an important role in mental health and wellbeing in persons with disabilities, although findings are less consistent than in general populations and strength of associations vary between constructs. Integrating persons with disabilities into social networks seems not sufficient and rehabilitation professionals together with affected persons and their peers should ensure that high quality relationships and tailored support are available.
Disability is a growing public health problem, not least in ageing populations worldwide . People with functional limitations or bodily impairments are generally disadvantaged in their opportunities to participate in social life . These restrictions not only contradict basic human rights , but may also affect people’s health and wellbeing. There is consistent evidence that continued favourable exchange with one’s proximate social environment (e.g. family, friends and work life) exerts beneficial effects on health and wellbeing . Conversely, social isolation or lack of close social ties is associated with poor health and increased mortality risk . These associations hold true for the general population but are particularly relevant for persons with physical disabilities, due to their restricted social participation . Reduced mental health in terms of psychiatric disorders is one of the major burdens of disease worldwide  and in particular in populations with disabilities .
There is convincing evidence that poor social relationships negatively impact mental health [9, 10]. So far, systematic reviews have summarized the links between social relationships and mental health in able-bodied populations , yet, no systematic review has been performed to document the current state of research in persons with physical disabilities. Traditionally, mental health is understood as a multidimensional construct of disease orientated symptoms [11, 12]. Given the pervasive effects of disability on major areas of everyday life, it is important to consider the subjective appraisal of one’s wellbeing. More precisely, wellbeing defined as the subjective appraisal of one’s functioning, mood and satisfaction with life complements the concept of mental health to represent this important dimension . This review incorporates this distinction by analyzing the associations of social relationships separately for mental health and wellbeing.
Given the variety of concepts and measures of assessing social relationships, we first define the leading concepts as a prerequisite to structure the bulk of information provided by the extensive body of empirical data. The term social relationships encompasses a wide variety of aspects relating to the proximal and distal social environment. Distal environment includes the broader social structure of opportunities for social integration (e.g. cultural, labour market, neighbourhood) and its quality (e.g. social capital) [9, 14]. Aspects of the distal social environment are excluded from this review as direct effects on health and wellbeing are usually weak or absent after analyzing their mediation through proximal factors , and as evidence for populations with disabilities is widely lacking. Our work therefore focuses on two leading sociological concepts that analyse proximal factors of social relationships, namely social networks and social support . Social networks describe the size, density, frequency and duration of social contacts , whereas social support emphasizes the functional significance in terms of providing instrumental, emotional or informational resources . Important further aspects concern the quality of and satisfaction with support received and the distinction between perceived and received support. Further aspects look at the dynamics of specific relationships, for example the relationship quality  of dyadic couples or family functioning [19, 20]. Not all social interactions result in positive relationships and negative social interactions will also form a part of this review . Finally the notion of loneliness is relevant in this context because the subjective feeling that it represents may have adverse effects on mental health and wellbeing, even in the presence of social contacts [22, 23]. We explore these aspects of social relationships from the perspective of persons with physical disabilities in order to assess how their perception of their interaction with the social environment is associated with mental health and wellbeing. Aspects of informal caregiving are not explicitly included in this review but may arise due to the inclusion of family functioning and received social support.
The objective of this review is thus to summarise a complex and heterogeneous body of empirical research on the association of different social relationship constructs with mental health and wellbeing in physical disability and to highlight conceptual and methodological deficiencies in the field of research.
The literature search included original articles published in English between January 1, 1995 and May 31, 2016. This time frame was selected due to feasibility issues and in order to assess the contemporary social environment. Moreover, a selective screening of the literature before 1995 showed that the main findings of these studies fully support the conclusion of our review and therefore would not provide a significant extension of knowledge. The databases PubMed, PsycINFO and SCOPUS were searched. SCOPUS is worldwide the largest abstract and citation database of peer-reviewed literature and PubMed and PsycINFO were used due to their relevance to the review’s objective and scope. To capture a comprehensive sample of relevant articles, we used multiple search terms for ‘social relationships’ and ‘physical disability’ including but not limited to the terms interpersonal relations, social environment, social isolation, social networks, relationship quality and disabled persons, activities of daily living, functional limitations, chronically ill. We also included search terms for the following common health conditions spinal cord injury, stroke, multiple sclerosis, rheumatoid arthritis and Parkinson’s disease, as many studies on persons with disabilities identify specific health conditions in their keywords rather than general terms relating to disability (see Appendix 1 for full search strategy). The disability terms were intended to identify papers where the study population had functional limitations in activities of daily living due to physical impairments or mobility restrictions, and not study populations which were restricted due to intellectual, developmental or mental impairments. We only included study populations with a diagnosed health condition leading to a disability, for example, studies on general ageing populations were excluded. The social relationship term did not include aspects associated with the distal social environment, such as culture, social capital and social cohesion as explained in the Background .
As a quality assessment for reporting, the PRISMA statement was adopted .
Inclusion and exclusion criteria
Original studies were eligible if they provided quantitative data regarding adults’ (≥ 18 years old) mental health or wellbeing outcomes as a function of social relationships, including both functional and structural aspects. In line with the literature, the term mental health was used to address health conditions (ICD-10 defined conditions, e.g., major depression) as well as mental functioning (e.g., SF-36 mental health subscale). Wellbeing was defined as a multidimensional concept which contains subjective appraisals of different aspects of life, including but not restricted to health. In line with the traditional understanding of subjective wellbeing described by Diener et al. [13, 25], we included studies that used the concept of wellbeing related to how individuals experience their quality of life including emotional reactions and cognitive evaluations of the satisfaction with general and specific life areas. Some studies subsumed established measures on general health as wellbeing or quality of life. We have only included these studies if they reported on a component of mental health. Mental health and wellbeing were not included in the search strategy in order to avoid potentially relevant studies being overlooked.
After removing duplicates (n = 910) and studies not in English language (n = 17), 5528 abstracts were screened based on predefined inclusion and exclusion criterion concerning topic, methodology, and study population. We excluded studies on a thematic basis if the topic was irrelevant to social relationships and health, if social relationships were not treated as an independent variable or if social relationships were not associated to a mental health or wellbeing outcome (n = 4623). We excluded studies on a methodological basis if the sample size was below 50, if social relationships were not assessed by a validated measurement instrument, if qualitative methodology was applied or if the article was an editorial or a review (n = 454). These criteria were applied to ensure that included studies were comparable and that studies with limited statistical power due to a low sample size were excluded. The inclusion of only those studies using validated instruments i.e. those psychometrically tested, aimed to ensure that social relationship concepts were adequately measured. Furthermore, studies focussing on persons other than those with physical disabilities (e.g., caregivers, health care providers) or persons with intellectual, developmental or mental disabilities were excluded (n = 203). In total, n = 231 full-text articles were screened for inclusion and n = 63 articles were included in our review. After full-text screening, n = 98 studies were excluded based on the topic, n = 44 based on methodology and n = 25 based on the study population (Fig. 1).
HT screened all abstracts ascertaining the relevance of the study and applying the inclusion and exclusion criteria. Double screening was performed on 5% of abstracts due to feasibility and a high level of reviewer agreement (94%). In case of uncertainty, the full-text was obtained and included in the full-text screening. HT screened all full-texts and 20% of full-texts were double screened by CF, with a reviewer agreement of 100%. If there was any indecision about the inclusion of an article this was discussed and if necessary, a third reviewer was consulted (JS).
To standardise data collection, a Microsoft Access 2010 database was created to extract the following information: First author, year of publication, country, sample size, study design, participant characteristics (age, gender, disability), independent and dependant variables, measurement instruments, effect sizes from bivariate and multivariable analyses, measure of variance and confounding variables controlled for. When several models presenting different confounders were reported, the fully-adjusted models were selected for data extraction. Multiple effect sizes were extracted from those studies that measured several associations between different aspects of social relationships and mental health or wellbeing. Effect sizes from every time point in longitudinal studies were extracted. When studies reported results separately for sub-groups of participants, the specific findings for each sub-group were recorded along with overall results. For quality assurance, data extraction was conducted by two independent reviewers for 10% of the included studies. Reviewer agreement here was 100%.
All included studies were assessed independently for quality of reporting by HT and CF using the Strengthening the Reporting of Observational studies in Epidemiology (STROBE) guidelines . STROBE is a quality assessment tool for observational studies which consists of 22 criteria to evaluate the reporting of the background, study design, data collection and data analysis of the study. This resulted in a score for each study ranging from lowest quality (0) to highest quality (22). For ease of interpretation the STROBE score was converted into a low (8–11), medium (12–15) and high (16–22) quality rating.
Study and participants characteristics of included studies are described (Table 1). To synthesise evidence, the details of each study including country, sample size, measures of social relationships and mental health or wellbeing, quality rating, participant characteristics and key findings were entered in Table 2 for cross-sectional and Table 3 for longitudinal studies. Key findings of cross-sectional studies are reported by declaring the variables under study, the direction of the association (+ for positive association; – for negative association; 0 for no association) and whether the association was statistically significant or not (+ and – indicate statistically significant results with p ≤ 0.05; + or – in brackets indicate non-significant results). Given the complexity of reporting longitudinal results, key findings of prospective studies were described in text form.
Due to the heterogeneity of both independent and dependent variables, a meta-analysis was not feasible. Instead, the results from included studies were combined into a narrative synthesis to draw conclusions . In comparison to meta-analysis, which uses statistical techniques to derive a pooled estimate of the effect size, narrative synthesis focuses primarily on the use of text to explain and summarise results from multiple studies. In this narrative synthesis, we grouped studies into thematically or conceptually related categories to study the amount of studies looking at certain themes and the number of associations between different social relationship constructs and mental health or wellbeing. We also considered the strength, direction, statistical significance and consistency of associations and additionally took into account potential change over time or differences in associations between subgroups.
Table 1 shows an overview of the social relationship, mental health and wellbeing constructs under study along with the participant characteristics of the included studies. The vast majority of the 63 included studies focussed on social support (n = 58), with relatively few other constructs being identified: Social networks were assessed in six studies, negative social interaction in three studies, family functioning in two studies, and relationship quality in one study. Concerning mental health and wellbeing constructs, depression was the most heavily studied construct being reported by 33 studies, a composite mental health score was reported by ten studies, followed by anxiety (n = 8), psychological distress (n = 7), posttraumatic stress disorder (n = 3), and hopelessness (n = 1). The health condition most prolifically studied was rheumatoid arthritis, particularly due to the inclusion of several studies from a large scale European-wide study focusing on social support in arthritis (EURIDISS) . The mean STROBE sum score was 13.5, ranging from 8 to 19. The description of any efforts to address potential sources of bias (met by 9.5% of included studies) and the explanation of how the study size was arrived at (met by 7.9% of included studies) were the two STROBE criteria which were most frequently unmet.
Tables 2 and 3 provide a summary on characteristics and key findings of included cross-sectional and longitudinal findings, respectively. Results are presented along the social relationship constructs I) social support, II) social networks, III) negative social interactions, IV) family functioning and V) relationship quality. For all five constructs, we first present an overview on study characteristics (specification of constructs, measurements, study quality), followed by an in-depth discussion on cross-sectional and longitudinal findings.
Of the 58 studies focussing on social support, 45 were cross-sectional and 13 longitudinal. Social support constructs were operationalized heterogeneously, including type (emotional, instrumental, affective or tangible) or source (e.g., family, friends, significant other) of social support, overall measures of perceived or received social support, satisfaction with support, negative social support or unavailability of support. Four studies assessed received social support, defined as actual exchange of support [29,30,31,32]. Six studies report their results according to type of social support [31,32,33,34,35,36]. Two studies looked at negative or problematic social support [37, 38], two at the unavailability of social support [37, 39], and three studies distinguished between the source of social support (friend, family, significant other) [40,41,42]. The remaining 44 studies investigated perceived social support or satisfaction with support, although precise definitions of the terms under study were often missing. This heterogeneity of used constructs is reflected by the fact that we found a total of 21 different measures to assess social support. Overall, we did not observe any systematic association between study quality and strength of associations for studies including a social support measure.
Cross-sectional findings. 33 of the 45 cross-sectional studies found a significant association between social support and mental health and/or wellbeing, while three studies reported a non-significant trend [43,44,45], two studies showed no association [46, 47] and seven did not test the association in multivariable analyses [30, 48,49,50,51,52,53].
More specifically, of the 25 studies assessing depression, 14 found an inverse association between some element of social support and depression [29, 33, 34, 37,38,39, 42, 54,55,56,57,58,59,60], six studies reported a trend towards an inverse association [43, 45, 61,62,63,64], and one observed no association . Two studies tested associations only in bivariable analyses and found no significant correlations [30, 53]. As mainly composite scores of social support were used, it was not possible to identify whether a certain aspect of social support was more protective than another. Of the four studies assessing anxiety, none reported a consistent association [53, 61, 64, 65]. A total of three studies looked at posttraumatic stress disorder (PTSD). While two of them only performed bivariable analysis [48, 66] one found a negative association between social support provided by friends and PTSD . Of the nine studies assessing composite scores of mental health, seven found a positive association [41, 67,68,69,70,71,72]. Of the 14 studies assessing wellbeing, eight reported a positive association in multivariable analysis [33, 58, 63, 64, 73,74,75,76] and three studies did not report the results for multivariable analysis as bivariable associations were insignificant [49,50,51].
Longitudinal findings. Of the included longitudinal studies, 15 out of 16 involved a social support construct (Table 3). Results suggest that at very early stages of the disease process social support increased over time [35, 77] only to decrease at later stages [31, 78]. Four studies looked at social support’s association with psychological distress [35, 78,79,80]. Three of these studies found a change in psychological distress over time as a function of social support [78, 80, 81], whereas one study only found cross-sectional associations . The one study only which distinguished between emotional and instrumental support observed associations of distress with emotional support but not with instrumental . Seven studies analysed the association between social support and depression, two of these studies showed evidence of a longitudinal relationship between social support and depression [82, 83], i.e. earlier measures of social support effecting depression at later time points. Three studies only found cross-sectional associations [36, 77, 84] and two studies could not observe any association between social support and depression [85, 86]. The three studies addressing anxiety as an outcome showed no longitudinal associations with social support [84,85,86].
Four cross-sectional studies included a measure of social networks as an independent variable (Table 2) [65, 76, 87, 88]. All measures of social networks addressed the size of network in terms of the frequency of interaction with different members or organisations of the network. Associations to depression were limited to men in one study  or to both men and women in a study of low quality . There were no significant associations of social networks with a composite measure of mental health , anxiety , or wellbeing .
Of the included longitudinal studies, two out of 16 included social networks as an independent variable (Table 3) [84, 86]. Both studies assessed the same population at different time points and were of low quality. In both studies, social networks showed weaker associations with depression and anxiety than perceived social support. One study found a negative association between social network in terms of number of friends shortly after diagnosis and depression 1 year later .
Negative social interactions
Three cross-sectional studies looked at negative social interaction (Table 2) [45, 65, 68]. Aspects of negative social interaction included lack of understanding, criticism and negative spousal responses to pain. All of these studies were medium in quality, two of which solely focused on interactions within partnerships [45, 65], whereas one also investigated negative responses from different sources such as family members and colleagues . All three studies provide evidence for associations with mental health: Negative associations between discounting, lack of understanding and mental health were found to be statistically significant , along with positive associations of criticism with anxiety , and of negative partner responses to pain with depression .
Two studies looked at family functioning [37, 89], one of high quality  and one of low quality . Inverse associations of family functioning with depression [37, 89] and negative affect , and positive associations with life satisfaction were found , but none with hopelessness . Effect sizes of associations of family functioning with negative affect and depression were similar to those of social support, but somewhat larger for associations with life satisfaction .
The one cross-sectional study which assessed relationship quality found an inverse relationship between relationship quality and depression . This cross-sectional finding was supported in an additional longitudinal study, although there was no evidence of a longitudinal association . Both studies were rated medium in quality.
In this review, we summarised a complex and heterogeneous body of empirical research on associations of social relationships with mental health and wellbeing in physical disability. When basing conclusions solely on results reported from multivariable analyses, we found consistent associations between social support and composite scores of mental health. The associations of social support with anxiety, depression and wellbeing were less pronounced as many studies reported insignificant associations. Remarkably, social networks seem to be related to depression, but not to any of the other studied measures on mental health or wellbeing. In contrast, family functioning, negative social interactions and relationship quality showed consistent associations with indicators of mental health and wellbeing, although the evidence was limited due to the small number of studies focusing on these concepts.
The aspect of social support is particularly dominant in disability research. Social support is considered a vital resource for hindering the negative consequences of a wide variety of stressors in disability (the ‘buffering hypothesis’ of social support ), including the chronic stress of physical disability itself. However, the number of studies which found insignificant or weak associations of social support with depression indicates limited support for this hypothesis. A review looking at social relationships and depression in the general population found 91.4% of studies to report a significant inverse association between social support and depression , in comparison we found only 59.0% of studies to report such an association. Moreover, the composite scores of social support which were often used in analysis integrated many distinct aspects of social support, often including items assessing received support alongside those assessing perceived support thus making it difficult to disentangle how different aspects of social support affected mental health and wellbeing. Inconsistent associations between social support and depression may therefore be explained by the potentially adverse effects of receiving social support in disability. Unwanted or unnecessary receipt of instrumental social support may have negative consequences among persons with disabilities, leading to reduced autonomy, self-worth and personal responsibility, all factors which are related to mental health and wellbeing . Furthermore, when learning to interact with people in times of stress, such as during the adjustment and adaption to disability, high levels of social support could lead to higher levels of psychological distress. Moreover, increased support may be recognised or mobilised during times of distress, thus increasing the complexity of the relationships and the potential for reverse causality . Evidence for the association of received instrumental support with mental health and wellbeing was lacking in this review, perhaps owing to the fact that long-term received support is often termed as ‘informal care’ in the literature.
The observation of inconclusive associations of social networks with indicators of mental health and wellbeing might be explained by the fact that social networks exert an indirect rather than direct effect on mental health and wellbeing . This explanation is consistent with the conceptual model devised by Berkman et al. which suggests that social support is a resource attainable through access to the upstream factor of social networks . This would suggest that social networks are important in their provision of social support but that their direct effect on mental health is minor. These results support the hypothesis by Cohen and Wills that qualitative support is more significant than social integration for persons under stress, i.e. persons with disabilities . Additionally, extensive networks may not necessarily be supportive and members of social networks may be a source of stress or conflict .
Potentials for future research
This review is based on an area of research that needs further development. One major limitation of this field of research concerns an inherent problem of the social relationships literature and refers to the potential tautology in the association between social relationships and distress. Although not significant in all cases, research indicates a clear trend towards an association between social relationships and mental health and/or wellbeing. As the majority of studies were cross-sectional, reverse causation in these findings cannot be excluded. It is evident that depressed or anxious people, for example, have trouble with social and interpersonal relationships and thus report lower social support or worse relationship quality . To overcome this challenge and to meaningfully study this potentially tautological relationship, future studies should be based on longitudinal data and be grounded in well-reasoned theories that provide testable hypotheses. Ideally, a sound theoretical foundation should drive the instrumentation and the hypotheses, and ultimately, the interventions.
A further shortcoming of this area of research might be seen in the fact that several important aspects of social relationships such as loneliness, autonomy or reciprocity in social relationships remained unexplored and are therefore not tested in disability despite their importance in the general population [97, 98]. Moreover, potentially interesting concepts such as relationship quality, family functioning or negative social interactions were only tested in a marginally low number of studies. A greater insight into these domains would lead to better understanding of the complex roles different aspects of social relationships play in persons with disabilities. Moreover, it would be worthwhile to include different social relationship constructs within studies to investigate its potentially different effects on health.
A further and common limitation in disability research is the use of convenience samples recruited from specific inpatient or outpatient settings, or through patient organisations. This may limit the generalisability of the included studies by restricting the analysis to a niche group of individuals from a certain context . Another methodological shortcoming concerns the quality of statistical analysis as we observed a restriction of analysis to bivariable associations without any adjustment for potential confounding in a number of studies. Also, we observe a lack of standardisation and homogeneity in the measurement of concepts, as for example 28 different instruments were used to measure social relationships, thus compromising the comparability of results.
Limitations and strengths of this review
The study is subject to several limitations. Firstly, search terms for physical disability included only selected health conditions, meaning that the search was biased towards these conditions and may have missed papers addressing the theme of social relationships in other disabling conditions. Secondly, no meta-analysis could be performed due to the heterogeneity of measurements. Thirdly, as we only included studies using validated instruments, we may have missed new dimensions in research and focused too heavily on established areas in social relationship research, such as social support. Overall, 26 studies were excluded as they did not assess social relationships with a validated measurement instrument. We would therefore urge researchers to develop psychometrically tested instruments which give validated results for aspects of social relationships such as reciprocity. The search was also limited to papers published in peer-reviewed journals in English creating publication bias. Finally, the time frame of the literature search was restricted to 1995–2016. For feasibility reasons, we did not include previous research findings, but selective screening of the literature before 1995 confirmed consistency with the mainstream research represented in our review.
These limitations were balanced by several strengths. In our review, we structured a broad and heterogeneous field of research in terms of theoretical concepts of social relationships. Moreover, by distinguishing between mental health and wellbeing, we demonstrated the relevance of subjective appraisal of functioning and mood, aspects which are often unnoticed in traditional research on mental health. By summarising current evidence we were able to identify under and over researched areas in the field and at the same time demonstrated substantial methodological shortcomings. By doing so, we provide recommendations for promising future research developments. Despite predefined inclusion criteria (e.g. timeframe, language, and methodological issues), the literature search proved to be comprehensive, with the screening of over 5000 articles.
We conclude that social relationships play an important role in mental health and wellbeing in persons with disabilities, although findings are less consistent than in the general population, strength of associations vary between constructs, and some important constructs such as loneliness, relationship quality or reciprocity are neglected in disability research. Integrating persons with disabilities into social networks is an important endeavour, however, it is of equal importance to strengthen the quality of their relationships and to tailor the level and kind of support to their needs. To promote mental health and wellbeing, rehabilitation professionals should support persons with disabilities and their significant others to ensure that high quality relationships are established and maintained, and that adequate support is available.
European Research on Incapacitating Diseases and Social Support
International Classification of Diseases, version 10
Preferred Reporting Items for Systematic Reviews and Meta-Analyses
Post-Traumatic Stress Disorder
36-Item Short Form Health Survey
Strengthening the Reporting of Observational Studies in Epidemiology
World Health Organization & World Bank. World report on disability. Geneva, Switzerland: World Health Organization; 2011.
Bickenbach JE, Chatterji S, Badley EM, Üstün T. Models of disablement, universalism and the international classification of impairments, disabilities and handicaps. Soc Sci Med. 1999;48(9):1173–87.
The United Nations. Convention on the Rights of Persons with Disabilities. Treaty Series, 2515, 3; 2006.
Berkman LF, Kawachi I, Glymour MM. Social Epidemiology. 2nd ed. Oxford, UK: Oxford University Press; 2014.
Holt-Lunstad J, Smith TB, Layton JB. Social relationships and mortality risk: a meta-analytic review. PLoS Med. 2010;7(7)
Albrecht GL, Devlieger PJ. The disability paradox: high quality of life against all odds. Soc Sci Med. 1999;48(8):977–88.
Whiteford HA, Degenhardt L, Rehm J, Baxter AJ, Ferrari AJ, Erskine HE, Charlson FJ, Norman RE, Flaxman AD, Johns N. Global burden of disease attributable to mental and substance use disorders: findings from the global burden of disease study 2010. Lancet. 2013;382(9904):1575–86.
Scott K, Bruffaerts R, Tsang A, Ormel J, Alonso J, Angermeyer M, Benjet C, Bromet E, De Girolamo G, De Graaf R. Depression–anxiety relationships with chronic physical conditions: results from the World mental health surveys. J Affect Disord. 2007;103(1):113–20.
Kawachi I, Berkman LF. Social Ties and Mental Health. J Urban Health. 2001;78(3)
Santini ZI, Koyanagi A, Tyrovolas S, Mason C, Haro JM. The association between social relationships and depression: a systematic review. J Affect Disord. 2015;175:53–65.
World Health Organisation. ICD-10 Classifications of Mental and Behavioural Disorder: Clinical Descriptions and Diagnositic Guidelines. Geneva, Switzerland: World Health Organisation. 1992.
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders IV. Washington. American Psychiatric Association. 1994.
Diener E, Suh EM, Lucas RE, Smith HL. Subjective Well-Being: Three Decades of Progress Psychol Bull. 1999;125(2):276–302.
Berkman LF, Glass T, Brissette I. Seeman T E. From social integration to health: Durkheim in the new millenium Soc Sci Med. 2000;51:843–57.
Kawachi I, Berkman LF. Social Capital, Social Cohesion, and Health In: Social Epidemiology Second edn. Edited by Berkman LF KI, Glymour MM. New York Oxford University Press; 2014.
Bott E. Urban families: conjugal roles and social networks. Hum Rel. 1955;
Cassel J. The contribution of the social environment to host resistance. Am J Epidemiol. 1976;104(2):107–23.
Pierce GR, Sarason IG, Sarason BR, Solky-Butzel JA, Nagle LC. Assessing the quality of personal relationships. J Soc Pers Relat. 1997;14(3):339–56.
Miller IW, Epstein NB, Bishop DS, Keitner GI. The McMaster family assessment device: reliability and validity. J Marital Fam Ther. 1985;11(4):345–56.
Hoge RD, Andrews D, Faulkner P, Robinson D. The family relationship index: validity data. J Clin Psychol. 1989;45(6):897–903.
Rook KS. The negative side of social interaction: impact on psychological well-being. J Pers Soc Psychol. 1984;46(5):1097.
Holt-Lunstad J, Smith TB, Baker B, Harris T, Stephenson D. Loneliness and social isolation as risk factors for mortality: a meta-analytic review. Perspect Psychol Sci. 2015;10(2):227–37.
Cacioppo JT, Hughes ME, Waite LJ, Hawkley LC, Thisted RA. Loneliness as a specific risk factor for depressive symptoms: cross-sectional and longitudinal analyses. Psychol Aging. 2006;21(1):140.
Moher D, Liberati A, Tetzlaff J, Altman DG, The PRISMA Group. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. PLoS Med. 2009; 6(6).
Diener E. Subjective well-being. Psychol Bull. 1984;95(3):542–75.
von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP. STROBE initiative. The Strengthening the reporting of observational studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet. 2007;370(9596):1453–7.
Popay J, Roberts H, Sowden A, Petticrew M, Arai L, Rodgers M, Britten N, Roen K, Duffy S. Guidance on the conduct of narrative synthesis in systematic reviews. A product from the ESRC methods programme Version. 2006;1
Suurmeijer TP, Doeglas DM, Briancon S, Krijnen WP, Krol B, Sanderman R, Moum T, Bjelle A, Van Den Heuvel WJ. The measurement of social support in the ‘European research on incapacitating diseases and social support’: the development of the social support questionnaire for transactions (SSQT). Soc Sci Med. 1995;40(9):1221–9.
Cheng Y, Liu C, Mao C, Qian J, Liu K, Ke G. Social support plays a role in depression in Parkinson's disease: a cross-section study in a Chinese cohort. Parkinsonism Relat Disord. 2008;14(1):43–5.
Zhang H, Zhou T, Zhang Y, Xu Y. Correlation between social support and depression in elderly stroke patients in the sequelae stage from five communities of shanghai. China Neural Regener Res. 2011;6(19):1493–7.
Van Leeuwen CMC, Post MWM, Van Asbeck FWA, Van Der Woude LHV, De Groot S, Lindeman E. Social support and life satisfaction in spinal cord injury during and up to one year after inpatient rehabilitation. J Rehabil Med. 2010;42(3):265–71.
van Leeuwen CM, Post MW, van Asbeck FW, Bongers-Janssen HM, van der Woude LH, de Groot S, Lindeman E. Life satisfaction in people with spinal cord injury during the first five years after discharge from inpatient rehabilitation. Disabil Rehabil. 2012;34(1):76–83.
Abraido-Lanza AF. Social support and psychological adjustment among Latinas with arthritis: a test of a theoretical model. Ann Behav Med. 2004;27(3):162–71.
Suurmeijer T, Van Sonderen F, Krol B, Doeglas D, Van Den Heuvel W, Sanderman R. The relationship between personality, supportive transactions and support satisfaction, and mental health of patients with early rheumatoid Arthritis. Results from the Dutch part of the EURIDISS study. Soc Indic Res. 2005;73(2):179–97.
Benka J, Nagyova I, Rosenberger J, Calfova A, Macejova Z, Middel B, Lazurova I, van Dijk JP, Groothoff JW. Social support and psychological distress in rheumatoid arthritis: a 4-year prospective study. Disabil Rehabil. 2012;34(9):754–61.
Sit JW, Wong TK, Clinton M, Li LS. Associated factors of post-stroke depression among Hong Kong Chinese: a longitudinal study. Psychol Health Med. 2007;12(2):117–25.
Coty M-BW, Kenneth A. Problematic social support, family functioning, and subjective well-being in women with rheumatoid arthritis. Women Health. 2010;50(1):53–70.
Riemsma RP, Taal E, Wiegman O, Rasker JJ, Bruyn GA, van Paassen HC. Problematic and positive support in relation to depression in people with rheumatoid arthritis. J Health Psychol. 2000;5(2):221–30.
Bamer A, Cetin K, Johnson K, Gibbons L, Ehde D. Validation study of prevalence and correlates of depressive symptomatology in multiple sclerosis. Gen Hosp Psychiatry. 2008;30(4):311–7.
Danner GR, Cynthia L. Protective factors and posttraumatic stress disorder in veterans with spinal cord injury. Int J Rehab Health. 2000;5(3):195–203.
Krokavcova M, van Dijk JP, Nagyova I, Rosenberger J, Gavelova M, Middel B, Gdovinova Z, Groothoff JW. Social support as a predictor of perceived health status in patients with multiple sclerosis. Patient Educ Couns. 2008;73(1):159–65.
Jensen MP, Smith AE, Bombardier CH, Yorkston KM, Miró J, Molton IR. Social support, depression, and physical disability: age and diagnostic group effects. Disabil Health J. 2014;7(2):164–72.
Dirik G, Karanci AN. Psychological distress in rheumatoid arthritis patients: an evaluation within the conservation of resources theory. Psychol Health. 2010;25(5):617–32.
Dodd Z, Driver S, Warren AM, Riggs S, Clark M. Effects of adult romantic attachment and social support on resilience and depression in individuals with spinal cord injuries. Top Spinal Cord Inj Rehabil. 2015;21(2):156–65.
Stroud MW, Turner JA, Jensen MP, Cardenas DD. Partner responses to pain behaviors are associated with depression and activity interference among persons with chronic pain and spinal cord injury. J Pain. 2006;7(2):91–9.
Huang CY, Chen WK, Lu CY, Tsai CC, Lai HL, Lin HY, Guo SE, Wu LM, Chen CI. Mediating effects of social support and self-concept on depressive symptoms in adults with spinal cord injury. Spinal Cord. 2015;53(5):413–6.
Shao J, Zhang Q, Lin T, Shen J, Li D. Well-being of elderly stroke survivors in Chinese communities: mediating effects of meaning in life. Aging Ment Health. 2014;18(4):435–43.
Hatcher MB, Whitaker C, Karl A. What predicts post-traumatic stress following spinal cord injury? Br J Health Psychol. 2009;14(3):541–61.
Hilari K, Northcott S. Social support in people with chronic aphasia. Aphasiology. 2006;20(1):17–36.
Jaracz K, Pawlak M, Gorna K, Kolcz B, Woloszyn D, Kozubski W. Quality of life and social support in patients with multiple sclerosis. Neurol Neurochir Pol. 2010;44(4):358–65.
Kim P, Warren S, Madill H, Hadley M. Quality of life of stroke survivors. Qual Life Res. 1999;8(4):293–301.
Kivisild A, Sabre L, Tomberg T, Ruus T, Kõrv J, Asser T, Linnamägi Ü. Health-related quality of life in patients with traumatic spinal cord injury in Estonia. Spinal Cord. 2014;52(7):570–5.
Treharne GJ, Kitas GD, Lyons AC, Booth DA. Well-being in rheumatoid Arthritis: the effects of disease duration and psychosocial factors. J Health Psychol. 2005;10(3):457–74.
Bambara JK, Turner AP, Williams RM, Haselkorn JK. Perceived social support and depression among veterans with multiple sclerosis. Disabil Rehabil. 2011;33(1):1–8.
Beedie A, Kennedy P. Quality of social support predicts hopelessness and depression post spinal cord injury. J Clin Psychol Med Settings. 2002;9(3):227–34.
Gay MC, Vrignaud P, Garitte C, Meunier C. Predictors of depression in multiple sclerosis patients. Acta Neurol Scand. 2010;121(3):161–70.
Lewin A, Jöbges M, Werheid K. The influence of self-efficacy, pre-stroke depression and perceived social support on self-reported depressive symptoms during stroke rehabilitation. Neuropsychol Rehabil. 2013;23(4):546–62.
Phillips LJ, Stuifbergen AK. Structural equation modeling of disability in women with fibromyalgia or multiple sclerosis. West J Nurs Res. 2009;31(1):89–109.
Suh Y, Weikert M, Dlugonski D, Sandroff B, Motl RW. Physical activity, social support, and depression: possible independent and indirect associations in persons with multiple sclerosis. Psychol Health Med. 2012;17(2):196–206.
Esbensen BA, Østerlind K, Hallberg IR. Quality of life of elderly persons with cancer: a 6-month follow-up. Scand J Caring Sci. 2007;21(2):178–90.
Fyrand L, Wichstrøm L, Moum T, Glennås A, Kvien TK. The impact of personality and social support on mental health for female patients with rheumatoid arthritis. Soc Indic Res. 1997;40(3):285–98.
Kraaimaat FW, van Dam-Baggen CMJ, Bijlsma JWJ. Depression, anxiety and social support in rheumatoid arthritic women without and with a spouse. Psychol Health. 1995;10(5):387–96.
Müller R, Peter C, Cieza A, Post MW, Van Leeuwen CM, Werner CS, Geyh S. Social skills: a resource for more social support, lower depression levels, higher quality of life, and participation in individuals with spinal cord injury? Arch Phys Med Rehabil. 2015;96(3):447–55.
Rintala D, Robinson-Whelen S, Matamoros R. Subjective stress in male veterans with spinal cord injury. J Rehabil Res Dev. 2005;42(3):291–304.
Kraaimaat F, Van Dam-Baggen R, Bijlsma J. Association of social support and the spouse's reaction with psychological distress in male and female patients with rheumatoid arthritis. J Rheumatol. 1995;22(4):644–8.
Agar E, Kennedy P, King NS. The role of negative cognitive appraisals in PTSD symptoms following spinal cord injuries. Behav Cogn Psychother. 2006;34(4):437–52.
Geuskens G, Burdorf A, Evers A, Hazes J. Clear associations between demographic and psychosocial factors and health-related quality of life in patients with early inflammatory joint complaints. J Rheumatol. 2008;35(9):1754–61.
Kool M, Van Middendorp H, Lumley M, Bijlsma JWJ, Geenen R. Social support and invalidation by others contribute uniquely to the understanding of physical and mental health of patients with rheumatic diseases. J Health Psychol. 2013;18(1):86–95.
Osborne TL, Jensen MP, Ehde DM, Hanley MA, Kraft G. Psychosocial factors associated with pain intensity, pain-related interference, and psychological functioning in persons with multiple sclerosis and pain. Pain. 2007;127(1–2):52–62.
Raichle KA, Hanley M, Jensen MP, Cardenas DD. Cognitions, coping, and social environment predict adjustment to pain in spinal cord injury. J Pain. 2007;8(9):718–29.
Ritvo PG, Fisk JD, Archibald CJ, Murray TJ, Field C. Psychosocial and neurological predictors of mental health in multiple sclerosis patients. J Clin Epidemiol. 1996;49(4):467–72.
Schwartz C, Frohner R. Contribution of demographic, medical, and social support variables in predicting the mental health dimension of quality of life among people with multiple sclerosis. Health Soc Work. 2005;30(3):203–12.
Gottlieb A, Golander H, Bar-Tal Y, Gottlieb D. The influence of social support and perceived control on handicap and quality of life after stroke. Aging. 2001;13(1):11–5.
Hampton NZ. The affective aspect of subjective well-being among Chinese people with and without spinal cord injuries. Disabil Rehabil. 2008;30(19):1473–9.
Dupont S. Sexual function and ways of coping in patients with multiple sclerosis and their partners. J Sex Marital Ther. 1996;11(4):359–72.
Pitsilka DA, Kafetsios K, Niakas D. Social support and quality of life in patients with rheumatoid arthritis in Greece. Clin Exp Rheumatol. 2015;33(1):27–33.
Townend BS, Whyte S, Desborough T, Crimmins D, Markus R, Levi C, Sturm JW. Longitudinal prevalence and determinants of early mood disorder post-stroke. J Clin Neurosci. 2007;14(5):429–34.
Strating MMH, Suurmeijer TPBM, Van Schuur WH. Disability, social support, and distress in rheumatoid arthritis: results from a thirteen-year prospective study. Arthritis Care Res. 2006;55(5):736–44.
Demange V, Guillemin F, Baumann M, Suurmeijer TPBM, Moum T, Doeglas D, Briançon S, van den Heuvel WJA. Are there more than cross-sectional relationships of social support and support networks with functional limitations and psychological distress in early rheumatoid Arthritis? The European research on incapacitating diseases and social support longitudinal study. Arthritis Care Res. 2004;51(5):782–91.
Hilari K, Northcott S, Roy P, Marshall J, Wiggins RD, Chataway J, Ames D. Psychological distress after stroke and aphasia: the first six months. Clin Rehabil. 2010;24(2):181–90.
Benka J, Nagyova I, Rosenberger J, Calfova A, Macejova Z, Lazurova I, van Dijk JP, Groothoff JW. Social support as a moderator of functional disability’s effect on depressive feelings in early rheumatoid arthritis: a four-year prospective study. Rehabil Psychol. 2014;59(1):19–26.
Costa J, Gouveia JP. A new approach to explain the link between social support and depression in a 2-years arthritis rheumatoid sample. Is there any moderation effect of acceptance? Int J Psychol Psychol Ther. 2013;13(1):65–82.
Doeglas DM, Suurmeijer TPBM, van den Heuvel WJA, Krol B, van Rijswijk MH, van Leeuwen MA, Sanderman R. Functional ability, social support, and depression in rheumatoid arthritis. Qual Life Res. 2004;13(6):1053–65.
Evers AW, Kraaimaat FW, Geenen R, Bijlsma JW. Determinants of psychological distress and its course in the first year after diagnosis in rheumatoid arthritis patients. J Behav Med. 1997;20(5):489–504.
Curtis R, Groarke A, Coughlan R, Gsel A. The influence of disease severity, perceived stress, social support and coping in patients with chronic illness: a 1 year follow up. Psychol Health Med. 2004;9(4):456–75.
Evers AWM, Kraaimaat FW, Geenen R, Jacobs JWG, Bijlsma JWJ. Longterm predictors of anxiety and depressed mood in early rheumatoid arthritis: a 3 and 5 year followup. J Rheumatol. 2002;29(11):2327–36.
Berkanovic E, Oster P, Wong WK, Bulpitt K, Clements P, Sterz M, Paulus H. The relationship between socioeconomic status and recently diagnosed rheumatoid arthritis. Arthritis Care Res. 1996;9(6):457–62.
Nicassio PM, Kay MA, Custodio MK, Irwin MR, Olmstead R, Weisman MH. An evaluation of a biopsychosocial framework for health-related quality of life and disability in rheumatoid arthritis. J Psychosom Res. 2011;71(2):79–85.
Bellin MH, Zabel TA, Dicianno BE, Levey E, Garver K, Linroth R, Braun P. Correlates of depressive and anxiety symptoms in young adults with spina bifida. J Pediatr Psychol. 2010;35(7):778–89.
McPheters JK, Sandberg JG. The relationship among couple relationship quality, physical functioning, and depression in multiple sclerosis patients and partners. Fam Syst Health. 2010;28(1):48–68.
Robinson RG, Murata Y, Shimoda K. Dimensions of social impairment and their effect on depression and recovery following stroke. Int Psychogeriatr. 1999;11(4):375–84.
Cohen S, Wills TA. Stress, social support, and the buffering hypothesis. Psychol Bull. 1985;98(2):310.
Santini ZI, Koyanagi A, Tyrovolas S, Mason C, Haro JM. The association between social relationships and depression: a systematic review. J Affect Disord 2015; 175(0):53–65.
Fischer R, Boer D. What is more important for national well-being: money or autonomy? A meta-analysis of well-being, burnout, and anxiety across 63 societies. J Pers Soc Psychol. 2011;101(1):164.
Dwyer KA. Psychosocial factors and health status in women with rheumatoid arthritis: predictive models. Am J Prev Med. 1997;13(1):66–72.
Umberson D, Montez JK. Social relationships and health: a flashpoint for health policy. J Health Soc Behav. 2010;51(Suppl):S54–66.
Wahrendorf M, Ribet C, Zins M, Siegrist J. Social productivity and depressive symptoms in early old age–results from the GAZEL study. Aging Mental Health. 2008;12(3):310–6.
Chandola T, Marmot M, Siegrist J. Failed reciprocity in close social relationships and health: findings from the Whitehall II study. J Psychosom Res. 2007;63(4):403–11.
Fekete C, Segerer W, Gemperli A, Brinkhof MW. Participation rates, response bias and response behaviours in the community survey of the Swiss spinal cord injury cohort study (SwiSCI). BMC Med Res Methodol. 2015;15(1):80.
King RB. Quality of life after stroke. Stroke. 1996;27(9):1467–72.
Stuifbergen A, Brown A, Phillips L. Predictors and moderators of the disablement process in persons with multiple sclerosis. NeuroRehabilitation. 2009;24(2):119–29.
Wu Q, Mok B. Mental health and social support: a pioneering study on the physically disabled in southern China. Int J Soc Welf. 2007;16(1):41–54.
We thank the authors of the included studies.
HT is supported by a grant from the Swiss National Science Foundation (100017_153256/1). CF and JS are supported by the Swiss Paraplegic Foundation. The funding bodies had no role in the design of the study, the collection, analysis and interpretation of data and in writing the manuscript.
Availability of data and materials
All dataset are available in the respective publications.
HT developed the search strategy, screened all articles, led the data extraction and drafted the first version of the manuscript. CF completed double screening and double data extraction. HT, JS and CF conceptualised the research question, interpreted results and developed the final version of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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The original version of this article was revised to correct an error in Figure 1.
An erratum to this article is available at https://doi.org/10.1186/s12889-017-4448-8.
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Tough, H., Siegrist, J. & Fekete, C. Social relationships, mental health and wellbeing in physical disability: a systematic review. BMC Public Health 17, 414 (2017). https://doi.org/10.1186/s12889-017-4308-6
- Social relationships
- Social support
- Social networks
- Mental health
- Physical disability