Abstract
Sexual and gender minority (SGM) adolescents under age 18 are underrepresented in sexual health research. Exclusion of SGM minors from these studies has resulted in a lack of knowledge about the risks and benefits youth experience from sexual health research participation. Institutional Review Boards’ (IRB) overprotective stances toward research risks and requirements for guardian consent for SGM research are significant barriers to participation, though few have investigated SGM youth’s perspectives on these topics. This study aimed to empirically inform decisions about guardian consent for sexuality survey studies involving SGM youth. A total of 74 SGM youth aged 14–17 completed an online survey of sexual behavior and SGM identity, and a new measure that compared the discomfort of sexual health survey completion to everyday events and exemplars of minimal risk research (e.g., behavioral observation). Youth described survey benefits and drawbacks and perspectives on guardian permission during an online focus group. Participants felt about the same as or more comfortable completing the survey compared to other research procedures, and indicated that direct and indirect participation benefits outweighed concerns about privacy and emotional discomfort. Most would not have participated if guardian permission was required, citing negative parental attitudes about adolescent sexuality and SGM issues and not being “out” about their SGM identity. Findings suggest that sexual health survey studies meet minimal risk criteria, are appropriate for SGM youth, and that recruitment would not be possible without waivers of guardian consent. Decreasing barriers to research participation would dramatically improve our understanding of sexual health among SGM youth.
Original language | English (US) |
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Pages (from-to) | 1393-1409 |
Number of pages | 17 |
Journal | Archives of Sexual Behavior |
Volume | 46 |
Issue number | 5 |
DOIs | |
State | Published - Jul 1 2017 |
Funding
This study was supported by R01MD009561 from the National Institute on Minority Health and Health Disparities (PIs: Brian Mustanski and Celia B. Fisher). The content in this manuscript is solely the responsibility of the authors and does not reflect the views of the National Institutes of Health. All procedures performed in studies involving human participants were in accordance with the ethical standards of the Northwestern University and Fordham University IRBs and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
Keywords
- Adolescence
- Parental consent
- Research ethics
- Sexual behavior
- Sexual orientation
ASJC Scopus subject areas
- General Psychology
- Arts and Humanities (miscellaneous)