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Author Notes:

E-mail address: Samuel_McLean@med.unc.edu

SM conceived of the study.

NS, JS, AS, KB, IL, SLM, SAMR, KB, CR, ML, RCK, CN, KW and SM helped to design the final study protocol.

All authors reviewed the manuscript.

Competing interests: In the past 3 years, RCK received support for his epidemiological studies from Sanofi Aventis; was a consultant for Johnson & Johnson Wellness and Prevention, Sage Pharmaceuticals, Shire, Takeda; and served on an advisory board for the Johnson & Johnson Services Inc. Lake Nona Life Project.

RCK is a co-owner of DataStat, Inc., a market research firm that carries out healthcare research

Subjects:

Research Funding:

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.

Keywords:

  • pain
  • posttraumatic stress
  • sexual assault
  • Longitudinal Studies
  • Cohort study

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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Journal Title:

BMJ Open

Volume:

Volume 9, Number 11

Publisher:

, Pages e031087-e031087

Type of Work:

Article | Final Publisher PDF

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.

Copyright information:

© Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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