Publication

Protocol for the first large-scale emergency care-based longitudinal cohort study of recovery after sexual assault: The Women's Health Study

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Last modified
  • 05/14/2025
Type of Material
Authors
    Nicole A Short, Medical University of South CarolinaJenyth Sullivan, The University of North CarolinaApril Soward, The University of North CarolinaKenneth A Bollen, The University of North CarolinaIsrael Liberzon, Texas A and M University SystemSandra Martin, The University of North CarolinaSheila Rauch, Emory UniversityKathy Bell, Tulsa Police DepartmentCatherine Rossi, Forensic NursingMegan Lechner, University of Colorado at Colorado SpringsCarissa Novak, The University of North CarolinaKristen Witkemper, The University of North CarolinaRonald C Kessler, Harvard Medical SchoolSamuel A McLean, The University of North Carolina
Language
  • English
Date
  • 2019-11-01
Publisher
  • BMJ Publishing Group: Open Access
Publication Version
Copyright Statement
  • © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 2044-6055
Volume
  • 9
Issue
  • 11
Start Page
  • e031087
End Page
  • e031087
Grant/Funding Information
  • R01AR064700 funded by the following National Institutes of Health Institutes: NIAMS, NINDS, OD (ORWH), NINR, NIMH, and NICHD.
  • This work was supported by NIH R01 AR064700.
Supplemental Material (URL)
Abstract
  • Introduction: Worldwide, an estimated 10%-27% of women are sexually assaulted during their lifetime. Despite the enormity of sexual assault as a public health problem, to our knowledge, no large-scale prospective studies of experiences and recovery over time among women presenting for emergency care after sexual assault have been performed. Methods and analysis: Women ≥18 years of age who present for emergency care within 72 hours of sexual assault to a network of treatment centres across the USA are approached for study participation. Blood DNA and RNA samples and brief questionnaire and medical record data are obtained from women providing initial consent. Full consent is obtained at initial 1 week follow-up to analyse blood sample data and to perform assessments at 1 week, 6 weeks, 6 months and 1 year. These assessments include evaluation of survivor life history, current health and recovery and experiences with treatment providers, law enforcement and the legal system. Ethics and dissemination: This study is approved by the University of North Carolina at Chapel Hill's Institutional Review Board (IRB) and the IRB of each participating study site. We hope to present the results of this study to the scientific community at conferences and in peer-reviewed journals.
Author Notes
Keywords
Research Categories
  • Health Sciences, Epidemiology
  • Sociology, Demography

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