From: Time spent on health related activities associated with chronic illness: a scoping literature review
 | Author, Title & Year | Country | Disease (if specified) | Design and methods- survey, RCT, qualitative study | Sample size |
---|---|---|---|---|---|
1 | Bittman & Thomson. Invisible Support: The determinants of time spent in informal care. 2000. [11] | Australia | Â | Method: survey. Quantitative analysis of ABS Time Use Surveys and Survey of Disability, Ageing and Carers. Uses this secondary data re: time burden/ use among carers, with a major focus on non-coresidential vs coresidential care. | 14,315 carers |
Characteristics of care recipients and informal carers include: living arrangements of carers and care recipients, level of disability, household income, poverty rates and effects on various lifestyle features. | |||||
2 | Bittman et al. Making the invisible visible. The life and time(s) of informal caregivers. 2004. [12] | Australia | Â | Method: survey and diary. Quantitative data from surveys and diaries from Canadian (N= 10,749) and Australian (N= 14,000 approximately) bureaux used to explore and compare time burden and time use among carers and non-carers, as well as methodological issues in obtaining data and measuring time use and caring activities. | Multiple samples: patients and carers |
Main variables are co-residency and non-care responsibilities. | |||||
3 | Bittman, M. et al. The time cost of care. 2005. [13] | Australia | Â | Method: survey and diary. This paper contrasts two different measures of care time using survey questions or a diary. | Multiple samples: carers |
4 | Braithwaite, V. Bound to Care. 1990. [6] | Australia | Â | Method: qualitative, descriptive and survey. Overall, takes a sociological view of what a caregiver is/does and means, it's not just tasks and burden, but a relationship and a responsibility. | 138 carers |
Although dated, and focused on care-givers, does provide some early basic data on time and other burdens in caring. | |||||
5 | Corbin, J. & Strauss, A. Managing chronic illness at home: Three lines of work. 1985. [2] | USA | Mainly cardiovascular diseases, cancer, stroke, & spinal injuries. | Method: qualitative. Interviews and (auto) biographies of people with CI and their spouses. | 60 couples: patients and carers |
Uses the concept of "work" in managing CIs and types of work: illness, everyday and biographical work. | |||||
6 | Ettner, S. et al. Investing time in health: do socio- economically disadvantaged patients spend more or less extra time on diabetes self-care? 2009. [26] | USA | Diabetes | Method: survey. Comprehensive survey and statistical analysis, using several variables (education, marital status, income, minority group/ethnicity status, work status, clinical characteristics) but limited to one CI; looks at only foot care, exercise and (conflates) shopping/cooking. | 11,927 patients |
Objective: To examine associations between socioeconomic position and extra time patients spend on foot care, shopping/cooking, and exercise due to diabetes. | |||||
7 | Hu, P. & Reuben, D. Effects of managed care on the length of time that elderly patients spend with physicians during ambulatory visits. 2002. [24] | USA | Â | Method: survey. Cross-sectional analysis of the 1998 National Ambulatory Medical Care Survey. | 4,964 elderly patients |
8 | Infante, et al. How people with chronic illnesses view their care in general practice: a qualitative study. 2004. | Australia | Â | Method: qualitative. 12 focus groups. | 76 patients |
Objectives: To explore the perceptions of patients with chronic conditions about the nature and quality of their care in general practice. | |||||
9 | Ironmonger, D. The value of care and nurture provided by household work. 1994. [7] | Australia | Â | Method: survey. Comparative statistical analysis of mainly ABS survey data of aggregates hours for aged care and related household activities | Multiple samples: carers |
10 | Jenkins, C. Women, work, and care giving: How do these roles affect women's well-being? 1997. [8] | USA | Â | Method: survey. Statistical analysis of data from the 1988 National Survey of Families & Households (USA); how much time in care- giving and other activities, and effects on stress levels. | 14,500 female carers |
11 | Langa, K., et al. Informal caregiving for chronic lung disease among older Americans. 2002. [9] | USA | Lung disease | Method: survey. Multivariable regression models using data from the 1993 Asset and Health Dynamics Study by survey. | National population-based sample of 7,443 community- dwelling elderly patients >70. |
Measurements: Weekly hours of informal care giving, and imputed cost of caregiver time. | |||||
The average number of hours per week of informal care was calculated for: activities of daily living (ADL); and instrumental activities of daily living (IADL). | |||||
12 | McCoy, L. Time, self and the medication day: a closer look at the everyday work of 'adherence'. 2009. [17] | Canada | HIV | Method: qualitative. 21 interviews and 16 focus-groups with people taking antiretroviral drugs. | 79 patients |
13 | McKenna, K. et al. Comparison of time use, role participation and life satisfaction of older people after stroke with a sample without stroke. 2009. [21] | Australia | Stroke | Method: qualitative & time use diary. Interviews with 23 participants and data compared with a prior study. Interviews prompted participant recall using calendars and diaries. | 23 patients >65 yrs old 1– 3 yrs post-stroke (mean age |
74.2 years, 69.6% men) | |||||
14 | Paoletti, I. A half life: Women caregivers of older disabled relatives. 1999. [10] | Italy | Â | Method: qualitative. Interviews and discourse analysis. | 50 female paid and unpaid carers. |
15 | Pritchard, P. Doctors, patients and time. 1992. [25] | UK | Â | Method: Descriptive. A narrative description about time and time use, different kinds of time, from both patients' and Doctors' perspective, their perceptions of the other's perceptions of time and its use and value. | N/A |
16 | Reed, et al. Economic evaluation of home blood pressure monitoring with or without telephonic behavioral self-management in patients with hypertension. 2010. [31] | USA | Hypertension | Method: RCT (other). A prospective economic evaluation alongside a randomized controlled trial of 636 patients with hypertension participating in the study's 3 interventions. Medical costs were estimated using electronic data representing medical services delivered within the health system. Intervention-related costs were derived using information collected during the trial, administrative records, and published unit costs. | 636 patients. |
17 | Russell, L. et al. Time requirements for diabetes self-management: Too much for many? 2005. [18] | USA | Diabetes | Method: qualitative. A convenience sample of 8 certified diabetes educators to derive consensus-based estimates of the time required for all self-care tasks recommended by the American Diabetes Association. | 8 certified diabetes educators |
(concerning patient time use) | |||||
18 | Russell, L. et al. Health- related activities in the American Time Use Survey. 2007. [20] | USA | Â | Method: survey. Compilation and statistical analysis of ATUS survey data on Health-Related Activities in America. | 34,000 patients |
19 | Russell, L. et al. How much time do patients spend on outpatient visits?: The American Time Use Survey. 2008. [22] | USA |  | Method: survey. Compilation and statistical analysis of ATUS survey data on outpatient visits. | 1,621 random sample of patients from 2003–06 ATUS data, age >15 |
20 | Safford, M. et al. How much time do patients with diabetes spend on self-care? 2005. [19] | USA | Diabetes | Method: survey. Cross-sectional survey of 1482 diabetic patients enrolled in 3 northeastern United States managed care plans. Statistical analysis using and linear regressions. | 1,482 diabetic patients (57.9% >55 yrs) |
21 | Wolf, D. Valuing informal elder care. 2004. [14] | USA | Â | Method: modelling. Addresses through modelling the problem of attaching a monetary value to informal elder care, and why we should; uses NLTCS data to illustrate. | N/A |
22 | Yabroff, K. et al. Estimating patient time costs associated with colorectal cancer care. 2005. [23] | USA | Colorectal cancer | Method: survey. Quantitative, longitudinal and comparative time data for cancer/non-cancer care based on past studies and medical records (SEER-Medicare database), and estimates a monetary value of patients' time based on BLS wage rates. | 75,470 patients with matched controls |