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Age at first intercourse and subsequent sexual partnering among adult women in the United States, a cross-sectional study



Concurrency and serial monogamy may increase risk for STIs when gaps fall within the infectious period. This study examined the association between early sexual debut and concurrent or serial sexual partnering among heterosexual adult women.


We identified 6,791 heterosexually active women, ages 21–44, from the 2006–2010 National Survey of Family Growth, a multi-stage probability sample of women in the United States. Self-reported age at first intercourse was categorized as <15, 15–17 and ≥18 years (referent). Sexual partnering was defined as concurrency (within the same month), serial monogamy with either a 1–3 month, or ≥4 month gap between partners, or monogamy (referent) in the year prior to interview. Polytomous logistic models provided adjusted odds ratios (aOR) and 95% confidence intervals (CI).


Concurrent partnerships in the year prior to interview were reported by 5.2% of women. Serial monogamy with a 1–3 month gap was reported by 2.5% of women. Compared with women whose sexual debut was ≥18 years, those <15 years at sexual initiation had 3.7 times the odds of reporting concurrent partnerships (aOR: 3.72; 95% CI: 2.46-5.62). Women <15 years of age at sexual debut had twice the odds of serial monogamy with gap lengths of 1–3 months between partners (aOR1–3 months: 2.13; 95% CI 1.15-3.94) as compared to women ≥18 years at sexual debut.


Sexual debut at <15 years is associated with both concurrency and serial monogamy with 1–3 month gaps between partners in U.S. women aged 21–44.

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The mean age of sexual debut among American females is approximately 17 years [1]. Among females 15–24 years at interview, 15% had their first heterosexual vaginal intercourse before their 15th birthday, increasing with each year to 54% experiencing first intercourse by age 18 [2]. Adolescent girls who have their first intercourse at earlier ages are at risk for a variety of negative sexual health outcomes, including higher rates of sexually transmitted infections (STIs), [3-7] adolescent pregnancy, [4] increased number of sexual partners, [4,6] and experience of intimate partner violence (IPV) [8]. This group engages in more sexual and general health risk behaviors (e.g. drug and alcohol use) than their peers for the duration of adolescence [6,9,10]. Early age at sexual debut has been correlated with increased STI risk, having risky sexual partners, having sex under the influence of alcohol or drugs, [11] and persistent experience with IPV in adulthood [8]. Previously, we have shown that among adult sexually active fertile women, those <15 years of age at sexual debut are less likely to regularly use contraceptives [12] and have a higher risk of experiencing multiple unintended pregnancies relative to those whose age at sexual debut was 18 years of age or older [13]. The association between age at sexual initiation and sexual partnering in adulthood has not been explored in women living in the U.S.

Concurrent sexual partnerships, which are sexual relationships with temporal overlap, may accelerate the spread of STIs [14,15]. Similarly, serially monogamous relationships may also increase the risk of STIs [16]. If a person engages in a series of sexual relationships with short gaps in-between, they can still infect a second partner with certain STIs if the period of infectivity has not ended [16]. Thus, those in serially monogamous partnerships with short gaps may be behaviorally monogamous and biologically concurrent [15]. Few studies have identified correlates of heterosexual partnering in adulthood. African American adults, young adults, and individuals with early age at sexual debut have been previously shown to have higher rates of concurrent sexual partnerships [17-19]. Similarly, African American women, and those with low education and low income levels have a higher prevalence of serially monogamous relationships [16]. A 2012 qualitative study of African American women in Philadelphia identified that living in social environments where concurrency is common, where there is a high prevalence of never married women, high rates of incarceration resulting in partnership disruption and women’s economic dependence on others as factors contributing to concurrency [20]. Among young adults, relationship instability and social acceptance of sex with non-committed partners may contribute to the higher prevalence of concurrency [6,21].

Using a nationally representative sample, we sought to assess whether there was an association between timing of first heterosexual intercourse and subsequent sexual partnering in adulthood and to quantify any such relationship. We extended previous research by viewing sexual partnering with a four-level variable: concurrent sexual partnering, serial monogamy with a gap between partners of 1–3 months, serial monogamy with a gap between partners of ≥4 months and monogamous relationships in the year preceding the interview. Examining the association with serial monogamy is important as those in these relationships may still be at increased risk of STI transmission, if the gap between partners is sufficiently small [15,16]. We hypothesized that age at sexual debut would be associated with concurrent sexual partnerships and, to a lesser degree, serial monogamy.



We analyzed publicly available data from the 2006–2010 continuous National Survey of Family Growth (NSFG). The National Center for Health Statistics of the Centers for Disease Control and Prevention collects data on reproductive and family health among a multi-stage, probability sample of the non-institutionalized, civilian United States population of men and women aged 15–44 years. Adolescents as well as racial and ethnic minorities were oversampled to ensure adequate representation. The sampling methodology for the NSFG has been described in detail elsewhere [22]. During the years 2006–2010, the NSFG interviewed a cross-sectional sample of 12,279 women aged 15–44 years living in US households [22]. Trained interviewers conducted in-person interviews in respondents’ homes with Computer Assisted Personal Interview (CAPI) technology and Audio Computer Assisted Self-Interviewing (ACASI) for particularly sensitive questions about sexual behaviors. The ACASI part of the interview asked respondents how many male and female partners they had (over their lifetime and in the prior 12 months). The institutional review board at Brigham Young University approved this study as exempt.


We identified 6,791 eligible respondents; women who were at least 21 years of age at the time of interview, reported their first sexual intercourse to be voluntary, self-identified as heterosexual and reported having vaginal intercourse with at least one opposite sex partner in the year prior to interview. Male and female samples of the NSFG are collected as separate samples with many differences in the nature and language of the questions asked; for this reason we limited this analysis to women. We considered respondents 21 years of age or older as adults which is consistent with the National Institutes of Health definition [23]. Figure 1 illustrates sample exclusions.

Figure 1
figure 1

Sample eligibility criteria.

Operational definition of timing of sexual debut

Women were asked, “at any time in your life, have you ever had sexual intercourse with a man, that is, made love, had sex, or gone all the way?” Women were specifically instructed not to count oral or anal sex, heavy petting or other forms of sexual activity that did not involve vaginal penetration. Women answering yes to this question were then asked for the month and year of this first intercourse and her age at the time of first intercourse. To permit comparison to previous literature, [12,24,25] age at first sexual intercourse was categorized as <15 years, 15–17 years and ≥18 years.

Operational definition of sexual partnerships

Respondents were classified according their self-reported sexual partnerships in the 12 months before the interview: monogamy (referent group); serial monogamy with gap length 1–3 months; serial monogamy with gap length ≥4 months; and concurrency (within the same month). The CAPI survey asked each respondent the number of partners they had had vaginal sex with in the previous 12 months, as well as over their lifetime. Women were asked to report the date, in month and year, of first and last sexual intercourse with their most recent opposite-sex partners in the past year, and for any partners not identified as currently married to or cohabitating with the respondent, whether or not the partner was a current partner. Respondents reported the month and year of the first and last sexual intercourse for up to three sexual partners within the year before the interview. Monogamy was defined as reporting only one sex partner for at least some of the previous 12 months. Serial monogamy was defined as reporting two or more sex partners over the past 12 months but with no overlap of first/last sex dates of any other partners. Gap length was defined as the minimum length of time between 2 non-overlapping partners and dichotomized as 1–3 months and ≥4 months. We selected 1–3 months to coincide with a period of time most relevant for transmission of STIs [15,16]. Concurrency was defined as reporting 2 or more partners in the past 12 months with an overlap of any partner’s first sex date and the previous partner’s last sex date.

Potential confounders

A literature review identified sociodemographic variables, sexual history variables, and childhood characteristics associated with age at first intercourse and/or sexual partnering to be considered as potential confounders. We examined self-reported race [26-28] (white, non-Hispanic, black, non-Hispanic, Hispanic, or other, non-Hispanic), age at interview [26] (21–24 years, 25–29 years, 30–34 years, 35–39 years, or 40–44 years), respondent’s education attainment [26] (less than high school, high school graduate, or at least some college), current household income as a percentage of the federal poverty level [26] (FPL) (<100% FPL, 100-199% FPL, ≥200% FPL), and marital status [26] (never married, currently married or cohabitating, or formerly married). Because childhood and family factors, including socioeconomic status during childhood [29,30], are associated with earlier sexual intercourse [25,31] and more risky sexual practices including increased number of lifetime sex partners,[25,30] we considered these variables as potential confounders. Socioeconomic status during childhood was captured by self-reported highest level of parental education for both mother and father [27] (less than high school, high school graduate, or at least some college). For paternal education only, “no father figure” was retained as a valid category. Absence of a father in the home has meaning as a proxy for childhood socioeconomic status [32].

Condom use in the past year among respondents to the NSFG was measured using the question,“ Thinking back over the past 12 months, would you say you have used a condom with your partner for sexual intercourse every time, most of the time, about half of the time, some of the time or none of the time”. This variable was used to estimate condom non-use among women in concurrent and serially monogamous relationships.


To account for the complex sampling design and weighting of the NSFG, [33] SUDAAN (ver. 11, Research Triangle Institute, NC, USA) was used. We described the sociodemographic variables across the four-level sexual partnering outcome variable: concurrent partnerships, serial monogamy with a 1–3 month gap, serial monogamy with ≥4 month gap, and monogamous (referent). Chi-square was used to test for a difference in proportions. To estimate the association between timing of sexual debut and sexual partnering in adulthood while simultaneously adjusting for confounders, we conducted polytomous logistic regression. First, a crude model was developed. Then we considered sociodemographic variables and childhood factors as potential confounders using an iterative approach to understand which variables confounded the association between timing of sexual debut and sexual partnering. Although we considered variables that altered the odds ratio for sexual partnering by more than 10% as material confounders, we included all potential confounders in the final models when no loss of precision was realized to reduce the likelihood for residual confounding. We derived odds ratios (OR) and adjusted OR (aOR) and 95% confidence intervals (CI) from these models.


Concurrent partnerships in the year prior to interview were reported by 5.2% (n = 478) of women. Serial monogamy was reported by a total of 4% of women (n = 363), 2.5% with gaps between partners 1–3 months and 1.5% with gaps ≥4 months. Of women reporting serial monogamy, 25.9% reported one month gap between partners, 20.2% reported two months, 16.9% reported 3 months, 19.9% reported 4–5 months and the 17.1% reported ≥ 6 months between partners.

The mean age at first intercourse for women was 17.6 years (SE = 0.09). Women reporting concurrent partnerships in the last year had the youngest mean age at first intercourse (16.0 year; SE = 0.19) compared to serially monogamous women with 1–3 month gap (mean: 16.9 years; SE = 0.34), serially monogamous women with ≥4 months gap (mean: 17.1 years; SE 0.25) and monogamous women (mean: 17.7 years; SE = 0.09). Figure 2 shows the percentage of women with younger, average, and older age at first intercourse by sexual partnering status; 25% of women in concurrent partnerships were <15 years of age at first sex, compared to 21% of serially monogamous women with 1–3 month gaps, 9.1% of serially monogamous women with ≥4 month gaps and 11% of monogamous women. The median number of lifetime partners was 4 (Interquartile Range (IQR): 1–7). Concurrent women had the highest median number of lifetime partners (Median = 10; IQR = 6–20) followed by serially monogamous with 1–3 month gaps (Median = 7; IQR = 5–14), serially monogamous women with ≥4 month gaps (Median = 7; IQR = 4–11) and finally monogamous women (Median: 3; IQR: 1–6). Nearly a quarter of women in each sexual partnering group (23% concurrent; 25% gap of 1–3 months between partners, 25% gap ≥ 4 months between partners) reported never using a condom in the prior year.

Figure 2
figure 2

Age at first intercourse and sexual partnering among adult U.S. women in the year before interview.

The sociodemographic characteristics by sexual partnership status in the year preceding the interview are given in Table 1. The overall characteristics of women engaging in concurrent partnerships differed little from serially monogamous women with gaps 1–3 months whereas women with gaps ≥4 months were more similar to monogamous women. Among women with gaps of 1–3 months, 39% were 21–24 years old at interview compared to 30% of women reporting concurrency, 25% of women with ≥4 month gaps and 14% of monogamous women.

Table 1 Characteristics of adult women by sexual partnering in the year before interview

Monogamous women differed from concurrent and serially monogamous women on several important variables. The prevalence of concurrency and serial monogamy (for both gap lengths) decreased with increasing age at interview while the prevalence of monogamy increased slightly with increasing age. The proportion of monogamous women in married or cohabitating partnerships (77.8%) was greater than in the other three partnership groups (17.5% concurrent; 11.2% 1–3 month gap; 15.4% ≥4 month gap). A larger percentage of monogamous partners also reported higher income (61%, ≥200% FPL vs. roughly 50% in each of the other partnership groups) and fathers with less than a high school education (23.2% monogamous; vs. 16.9% concurrent; 15.0% serial with 1–3 month gap; 8% serial with ≥4 month gap). More women in concurrent (27%) and serially monogamous (20% 1–3 month gap; 29.6% ≥4 month gap) relationships self-identified as black, non-Hispanic race as compared to monogamous relationships (12.4%).

Table 2 displays the crude and adjusted odds ratios for age at first intercourse and sexual partnership style in adulthood. The logistic regression model is adjusted for maternal education, paternal education, marital status, race, age, education level, and income. The odds of concurrent partnership for those aged <15 years at first sex were 3.7 (95% CI: 2.46-5.62) times that of women 18 or older at first sex. The association between being <15 years at first sex and serial monogamy was limited to those with gaps of 1–3 months between partners. Specifically, those who experienced sexual debut before age 15 had 2.1 (95% CI: 1.15-3.94) times the odds of reporting serial monogamy with a gap of 1–3 months and no higher or lower odds or reporting serial monogamy with a gap of ≥4 months (aOR: 0.94; 95% CI:0.94-1.75), compared to those with sexual debut at ≥18 years. Women 15–17 years of age at first sex had odds of 1.6 times that of women with sexual debut at ≥18 years of reporting concurrent partnerships (95% CI: 1.14-2.24), but no higher or lower odds of reporting serial monogamy at either gap length (aOR1–3 months: 0.89; 95% CI: 0.55-1.45; aOR4+months: 1.11; 95% CI: 0.67-1.81).

Table 2 Association between age at first intercourse and sexual partnering in adulthood, overall and stratified by age at interview


Overall, 5.2% of adult women 21 years or older reported concurrent sexual partnerships and 4% reported serial monogamy in the year preceding interview. Of those reporting serial monogamy, the majority had a gap length of 1–3 months. We observed that age of sexual debut was associated with concurrency in adult women. Overall, compared to women ≥18 years at first sex, those <15 years of age and 15–17 years of age at their first intercourse had respectively, 3.7 and 1.6 times the odds of reporting concurrent partnerships in the year prior to interview, demonstrating increasing odds with decreasing age at first intercourse.

The estimate of concurrent sexual partnerships is similar in our study relative to other reports [34]. We estimate that approximately 4% of women were participants in serially monogamous relationships in the prior year. Previous estimates of serial monogamy have come from high risk clinic populations [15] or have been limited to populations of women with at least two sexual partners in the last year [21]. That age at sexual debut prior to age 15 years is strongly associated with concurrent sexual partnerships is supportive of the idea that early sexual experiences may have long-term impact on reproductive health. These data join a growing body of literature supporting the notion that a distal factor such as age at sexual debut remains important to sexual health outcomes in adulthood [10,11,13].

Although the NSFG does not specifically ask about condom use in overlapping relationships, we observed that nearly a quarter of women reporting concurrent and serially monogamous partnerships (23% concurrent; 25% gap of 1–3 months between partners, 25% gap ≥ 4 months between partners) reported never using a condom in the prior year, suggesting that many women participating in these partnerships may underestimate their STI risk. Of the women who reported serially monogamous relationships, the majority (83%) reported gaps of less than six months, within the infectivity period for some bacterial STIs, and more than half (63%) reported partnership gaps less than three months, the time frame during which HIV infectivity is thought to be highest [35] and within the infectivity period for many other common STIs including; chlamydia, gonorrhea, syphilis, HSV, and HPV [36].

Age at sexual initiation may be associated with a trajectory of negative sexual health outcomes; however the mechanism for this relationship remains unclear. Previous research has identified the roles of sensation-seeking and impulsivity in early sexual debut [37]. These genetically-influenced [38] personality characteristics likely persist into adulthood thus influencing adults to seek higher risk sexual experiences including multiple and non-committed partnerships. Sensation-seeking and impulsivity have been correlated with “hook-ups” (sex outside a committed relationship) among college-aged women [21]. Differences in self-control that are persistent from adolescence into adulthood may similarly affect early entry into sexual relationships and patterns of sexual partnering in adulthood [39]. Another hypothesized mechanism is attachment style. Secure attachment style has been positively associated with relationship quality and negatively associated with sexual risk taking [40]. Persons with avoidant attachment styles may be more likely to have had an early entry into sexual intercourse [41] and to employ methods of affect-regulation, including cycling in and out of sexual partnerships, to maintain emotional distance from romantic partners [42].

These data suggest that public health efforts should continue to support delaying initiation of sexual intercourse among youth at high risk for early debut and in reducing the risk of long-term reproductive consequences for youth and young-adults who have already had sex. It is important to note that a systematic review of programs aimed to reduce risky sexual behavior in adolescents conducted by the U.S. Department of Health and Human Services found wide variability in the effectiveness of these programs in reducing risk behaviors, including delaying sexual activity, suggesting that new and innovative approaches may be warranted [43]. Familial relationships and parental communication about sex have been shown to be effective in delaying sex. Integration of family components into sex-education programs has shown promise in delaying sexual initiation [44]. Historically, risk reduction programs for sexually experienced youth have focused on return to abstinence, use of condoms or contraceptive devices or reduced frequency of intercourse [30]. Our findings support the need to include skill-based messages on strategies for reducing risk such as the use of assertive statements and introduction of sex only with trusted partners [45].

The practical implications of the findings beyond adolescence must also be considered. More than half of sexually active young women aged 15–24 report having a pap smear in the prior year [46]. Annual pap testing and contraceptive prescription renewal provide regular clinical opportunities for counseling on sexual risk reduction. Including age at first intercourse on patient intake forms may assist providers in identifying women at higher risk for risky sexual behaviors. Others have shown that brief clinic-based counseling increases sexual health knowledge and lowers rates of STIs in young women [47].

The NSFG was not designed to delve deeper into why age at sexual debut is associated with sexual partnering patterns in adulthood. One possibility is that women whose sexual initiation is deferred to more than 18 years of age have a higher risk aversion in general. This possibility cannot be explored with the data available in the NSFG. We also cannot exclude the explanation that early intercourse represents an indicator for women who have increased attraction to risk. If this were the case, screening for risk tolerance in early adolescence could be useful. We did not include women who reported that their sexual debut was not voluntary. We recognize that non-voluntary sexual debut may have been under-reported.

This study has several important strengths. The NSFG provided a large, nationally representative sample, with oversampling of minority groups. Using sampling weights helps us to account for bias and improve the extent to which the data can be generalized to the U.S. population. To our knowledge no prior study among adult women has evaluated measures of both sexual concurrency and serial monogamy overall or with variable gap lengths or generated population estimates for the prevalence of serial monogamy or the distribution of gap length. The limitations of this study must also be considered. Previous research has acknowledged the challenge of accurately measuring sexual behavior [48,49]. The NSFG employed several techniques to improve reporting including the use of ACASI for particularly sensitive items and anchoring on a life-history calendar to improve reporting of dates [33]. Under-reporting of multiple partners among unmarried sexually active women aged 18 to 21 years may occur [50]. Misclassification of sexual partnering may have attenuated our measures of association; it is likely to have been non-differential with respect to age at sexual debut.


These data considered with other research suggest that age at sexual debut is an important distal factor which sets a trajectory of risky sexual behavior including sexual partnering patterns, contraceptive non-use, [12] and multiple unintended pregnancies [13]. These findings suggest that sexual debut before age 15 years is associated with concurrency and serial partnering with gaps 1–3 months through young and middle adulthood, which may increase risk for STIs well into adulthood. Study of serially monogamous relationships remains important due to their association with STI risk, particularly for serial partnering with gaps that fall within the infectious period for STIs [15,16,36]. Our findings add to the mounting evidence in support of interventions aimed to delay sexual initiation and increase the practice of safe sexual behaviors of all women.



Sexually transmitted Infection(s)


Intimate partner violence


National survey of family growth


Computer assisted personal interviewing


Audio computer assisted self-interviewing


Federal poverty level


Odds ratio


Adjusted odds ratio


Confidence interval


Interquartile range


Human immunodeficiency virus


Herpes simplex virus


Human papilloma virus


  1. Guttmacher Institute. American teens’ sexual and reproductive health. 2014;

  2. Finer LB, Philbin JM. Sexual initiation, contraceptive use, and pregnancy among young adolescents. Pediatrics. 2013;131(5):886–91.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Kaestle CE, Halpern CT, Miller WC, Ford CA. Young age at first sexual intercourse and sexually transmitted infections in adolescents and young adults. Am J Epidemiol. 2005;161(8):774–80.

    Article  PubMed  Google Scholar 

  4. Coker AL, Richter DL, Valois RF, McKeown RE, Garrison CZ, Vincent ML. Correlates and consequences of early initiation of sexual intercourse. J Sch Health. 1994;64(9):372–7.

    Article  CAS  PubMed  Google Scholar 

  5. Greenberg J, Magder L, Aral S. Age at first coitus a marker for risky sexual behavior in women. Sex Transm Dis. 1992;19(6):331–4.

    Article  CAS  PubMed  Google Scholar 

  6. Santelli JS, Brener ND, Lowry R, Bhatt A, Zabin LS. Multiple sexual partners among U.S. adolescents and young adults. Fam Plann Perspect. 1998;30(6):271–5.

    Article  CAS  PubMed  Google Scholar 

  7. Upchurch DM, Mason WM, Kusunoki Y, Kriechbaum MJ. Social and behavioral determinants of self-reported STD among adolescents. Perspect Sex Reprod Health. 2004;36(6):276–87.

    Article  PubMed  Google Scholar 

  8. Halpern CT, Spriggs AL, Martin SL, Kupper LL. Patterns of intimate partner violence victimization from adolescence to young adulthood in a nationally representative sample. J Adolesc Health. 2009;45(5):508–16.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Cavazos-Rehg PA, Krauss MJ, Spitznagel EL, Schootman M, Peipert JF, Cottler LB, et al. Type of contraception method used at last intercourse and associations with health risk behaviors among US adolescents. Contraception. 2010;82(6):549–55.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Ellis BJ, Bates JE, Dodge KA, Fergusson DM, Horwood LJ, Pettit GS, et al. Does father absence place daughters at special risk for early sexual activity and teenage pregnancy? Child Dev. 2003;74(3):801–21.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Sandfort TG, Orr M, Hirsch JS, Santelli J. Long-term health correlates of timing of sexual debut: results from a national US study. Am J Public Health. 2008;98(1):155–61.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Magnusson BM, Masho SW, Lapane KL. Early age at first intercourse and subsequent gaps in contraceptive use. J Womens Health. 2012;21(1):73–9.

    Article  Google Scholar 

  13. Magnusson BM, Masho SW, Lapane KL. Adolescent and sexual history factors influencing reproductive control among women aged 18–44. Sex Health. 2011;8(1):95–101.

    Article  PubMed  Google Scholar 

  14. Doherty IA, Shiboski S, Ellen JM, Adimora AA, Padian NS. Sexual bridging socially and over time: a simulation model exploring the relative effects of mixing and concurrency on viral sexually transmitted infection transmission. Sex Transm Dis. 2006;33(6):368–73.

    Article  PubMed  Google Scholar 

  15. Mercer CH, Aicken CR, Tanton C, Estcourt CS, Brook MG, Keane F, et al. Serial monogamy and biologic concurrency: measurement of the gaps between sexual partners to inform targeted strategies. Am J Epidemiol. 2013;178(2):249–59.

    Article  PubMed  Google Scholar 

  16. Kraut-Becher JR, Aral SO. Gap length: an important factor in sexually transmitted disease transmission. Sex Transm Dis. 2003;30(3):221–5.

    Article  PubMed  Google Scholar 

  17. Morris M, Kretzschmar M. Concurrent partnerships and the spread of HIV. AIDS. 1997;11(5):641–8.

    Article  CAS  PubMed  Google Scholar 

  18. Adimora AA, Schoenbach VJ, Martinson F, Donaldson KH, Stancil TR, Fullilove RE. Concurrent sexual partnerships among African Americans in the rural south. Ann Epidemiol. 2004;14(3):155–60.

    Article  PubMed  Google Scholar 

  19. Gorbach PM, Drumright LN, Holmes KK. Discord, discordance, and concurrency: comparing individual and partnership-level analyses of new partnerships of young adults at risk of sexually transmitted infections. Sex Transm Dis. 2005;32(1):7–12.

    Article  PubMed  Google Scholar 

  20. Nunn A, Dickman S, Cornwall A, Kwakwa H, Mayer KH, Rana A, et al. Concurrent sexual partnerships among African American women in Philadelphia: results from a qualitative study. Sex Health. 2012;9(3):288–96.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Fielder RL, Walsh JL, Carey KB, Carey MP. Predictors of sexual hookups: a theory-based, prospective study of first-year college women. Arch Sex Behav. 2013;42(8):1425–41.

    Article  PubMed  Google Scholar 

  22. Lepkowski JM, Mosher WD, Davis KE, Groves RM, Van Hoewyk J. The 2006–2010 national survey of family growth: sample design and analysis of a continuous survey. Vital Health Stat 2. 2010;150:1–36.

    Google Scholar 

  23. National Institutes of Health. Policy on guidelines for including children as participants in involving human subjects.

  24. Gómez AM, Speizer IS, Reynolds H, Murray N, Beauvais H. Age differences at sexual debut and subsequent reproductive health: Is there a link. Reprod Health. 2008;5(8).

  25. O'Donnell L, O'Donnell CR, Stueve A. Early sexual initiation and subsequent sex-related risks among urban minority youth: the reach for health study. Fam Plann Perspect. 2001;33(6):268–75.

    Article  PubMed  Google Scholar 

  26. Adimora AA, Schoenbach VJ, Bonas DM, Martinson FE, Donaldson KH, Stancil TR. Concurrent sexual partnerships among women in the United States. Epidemiology. 2002;13(3):320–7.

    Article  PubMed  Google Scholar 

  27. Mott FL, Fondell MM, Hu PN, Kowaleski-Jones L, Menaghan EG. The determinants of first sex by age 14 in a high-risk adolescent population. Fam Plann Perspect. 1996;13:8.

    Google Scholar 

  28. Cavazos-Rehg PA, Krauss MJ, Spitznagel EL, Schootman M, Bucholz KK, Peipert JF, et al. Age of sexual debut among US adolescents. Contraception. 2009;80(2):158–62.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Manlove J, Franzetta K, McKinney K, Papillo AR, Terry-Humen E. No time to waste: programs to reduce teen pregnancy among middle school-aged youth. Washington DC: National Campaign to Prevent Teen Pregnancy; 2004.

    Google Scholar 

  30. Manlove J, Ikramullah E. Not yet: programs to delay first sex among teens. Washington DC: National Campaign to Prevent Teen Pregnancy; 2004.

    Google Scholar 

  31. Resnick MD, Bearman PS, Blum RW, Bauman KE, Harris KM, Jones J, et al. Protecting adolescents from harm. Findings from the national longitudinal study on adolescent health. JAMA. 1997;278(10):823–32.

    Article  CAS  PubMed  Google Scholar 

  32. Fields J. Children’s living arrangments and characteristics, March 2002. U.S. Department of Commerce, Economics and Statistics Administration, US Census Bureau; 2002.

  33. Groves RM, Mosher WD, Lepkowski JM, Kirgis NG. Planning and development of the continuous national survey of family growth. Vital Health Stat 1. 2009;48:1–64.

    Google Scholar 

  34. Adimora AA, Schoenbach VJ, Taylor EM, Khan MR, Schwartz RJ. Concurrent partnerships, nonmonogamous partners, and substance use among women in the United States. Am J Public Health. 2011;101(1):128–36.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Hollingsworth TD, Anderson RM, Fraser C. HIV-1 transmission, by stage of infection. J Infect Dis. 2008;198(5):687–93.

    Article  PubMed  Google Scholar 

  36. Foxman B, Newman M, Percha B, Holmes KK, Aral SO. Measures of sexual partnerships: lengths, gaps, overlaps and sexually transmitted infection. Sex Transm Dis. 2006;33(4):209–14.

    PubMed  Google Scholar 

  37. Khurana A, Romer D, Betancourt LM, Brodsky NL, Giannetta JM, Hurt H. Early adolescent sexual debut: the mediating role of working memory ability, sensation seeking, and impulsivity. Dev Psychol. 2012;48(5):1416–28.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Harden KP, Quinn PD, Tucker-Drob EM. Genetically influenced change in sensation seeking drives the rise of delinquent behavior during adolescence. Dev Sci. 2012;15(1):150–63.

    Article  PubMed  Google Scholar 

  39. Moffitt TE, Arseneault L, Belsky D, Dickson N, Hancox RJ, Harrington H, et al. A gradient of childhood self-control predicts health, wealth, and public safety. Proc Natl Acad Sci U S A. 2011;108(7):2693–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Collins NL, Read SJ. Adult attachment, working models, and relationship quality in dating couples. J Pers Soc Psychol. 1990;58(4):644–63.

    Article  CAS  PubMed  Google Scholar 

  41. Bogaert AF, Sadava S. Adult attachment and sexual behavior. Pers Relat. 2002;9(2):191–204.

    Article  Google Scholar 

  42. Brennan KA, Shaver PR. Dimensions of adult attachment, affect regulation, and romantic relationship functioning. Person Soc Psychol Bull. 1995;21(3):267–83.

    Article  Google Scholar 

  43. Goesling B, Colman S, Trenholm C, Terzian M, Moore K. Programs to reduce teen pregnancy, sexually transmitted infections, and associated sexual risk behaviors: a systematic review. J Adolesc Health. 2014;54(5):499–507.

    Article  PubMed  Google Scholar 

  44. Grossman JM, Frye A, Charmaraman L, Erkut S. Family homework and school‐based sex education: delaying early adolescents’ sexual behavior. J Sch Health. 2013;83(11):810–7.

    Article  PubMed  Google Scholar 

  45. Morrison‐Beedy D, Passmore D, Carey MP. Exit interviews from adolescent girls who participated in a sexual risk‐reduction intervention: implications for community‐based health education promotion for adolescents. J Midwifery Womens Health. 2013;58(3):313–20.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Saraiya M, Martinez G, Glaser K, Kulasingam S. Pap testing and sexual activity among young women in the United States. Obstet Gynecol. 2009;114(6):1213–9.

    Article  PubMed  Google Scholar 

  47. Kamb ML, Fishbein M, Douglas Jr JM, Rhodes F, Rogers J, Bolan G, et al. Efficacy of risk-reduction counseling to prevent human immunodeficiency virus and sexually transmitted diseases: a randomized controlled trial. project RESPECT study group. JAMA. 1998;280(13):1161–7.

    Article  CAS  PubMed  Google Scholar 

  48. Minnis AM, Steiner MJ, Gallo MF, Warner L, Hobbs MM, van der Straten A, et al. Biomarker validation of reports of recent sexual activity: results of a randomized controlled study in zimbabwe. Am J Epidemiol. 2009;170(7):918–24.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Fenton KA, Johnson AM, McManus S, Erens B. Measuring sexual behaviour: methodological challenges in survey research. Sex Transm Infect. 2001;77(2):84–92.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Morrison-Beedy D, Carey MP, Tu X. Accuracy of audio computer-assisted self-interviewing (ACASI) and self-administered questionnaires for the assessment of sexual behavior. AIDS Behav. 2006;10(5):541–52.

    Article  PubMed  PubMed Central  Google Scholar 

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Correspondence to Brianna M Magnusson.

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The authors declare that they have no competing interests.

Authors’ contributions

BMM participated in the design of the study, performed the statistical analyses and is primarily responsible for the written text of the manuscript. JN conceived of the study and participated in its design and coordination and helped to draft the manuscript. KLL assisted with the analyses, participated in the interpretation of findings and helped to draft the manuscript. All authors read and approved the final manuscript.

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Magnusson, B.M., Nield, J.A. & Lapane, K.L. Age at first intercourse and subsequent sexual partnering among adult women in the United States, a cross-sectional study. BMC Public Health 15, 98 (2015).

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