PTSD and Risk Behavior in HIV Positive Female Adolescents
NCT ID: NCT00271882
Last Updated: 2017-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
40 participants
OBSERVATIONAL
2006-03-31
2006-09-30
Brief Summary
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Detailed Description
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The study will initially be conducted at three ATN clinical sites with approximately 20 females recruited per site for a total of 60 participants. Other ATN clinical sites may be allowed to participate in the future if the study is slow to accrue.
The participants consist of English speaking women, ages 18-24 years, who acquired HIV through heterosexual intercourse or injection drug use after the age of 9 years, reported a history of sexual and/or physical abuse prior to age 18, and engaged in vaginal or anal intercourse in the 4 months prior to screening.
Approximately half of the participants will report a recent history of substance use as defined by study criteria and approximately half of the participants will report no such history.
Eligible patients will be identified and screened by the ATN research staff at the participating sites. The Protocol Chair and trained Research Assistant will conduct the open-ended qualitative interviews using an open-ended script. The interview will be audio-taped and transcribed. Prior to the open-ended script interview, participants will be asked about Posttraumatic Stress Disorder symptoms, abuse history, substance use, sexual behavior, and demographics. Responses to these questions will not be audio-taped and will be entered into the ATN 053 database by the ATN site staff.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Female birth gender
* Verbal confirmation of acquisition of behaviorally-acquired HIV infection including from injection drug use (IDU) or heterosexual intercourse (vaginal, oral and/or anal) after the age of 9 years
* HIV-1 infection as documented by a positive result on any of the following licensed tests at any time: any antibody test confirmed by Western blot, HIV culture, plasma HIV-1 RNA PCR \> 1,000 copies/mL or a HIV DNA PCR
* History of physical and/or sexual abuse prior to age 18 years old documented by a Screening Questionnaire
* Voluntary vaginal and/or anal intercourse with a male within the 4 months prior to screening.
* Ability to understand and communicate in spoken English sufficient to provide informed consent and to be interviewed
* Availability of enrollment slots for the participant's assigned substance-use category at the time of the Screening Questionnaire. (Approximately half of the participants will report substance use) This will be monitored throughout the study enrollment period.
* Willingness to have the qualitative study interview audio-taped
* Willingness and ability to provide informed consent
Exclusion Criteria
* Visibly distraught and/or visibly emotionally unstable (e.g., depressive mood, exhibiting manic, suicidal, or violent behavior);
* Visibly intoxicated or under the influence of psychoactive agents; or
* Presents as acutely ill.
18 Years
24 Years
FEMALE
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
National Institute of Mental Health (NIMH)
NIH
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
NIH
University of North Carolina, Chapel Hill
OTHER
Responsible Party
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Principal Investigators
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Gretchen Clum, Ph.D
Role: STUDY_CHAIR
Tulane School of Public Health and Tropical Medicine
Locations
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University of Miami
Miami, Florida, United States
Montefiore Medical Center
The Bronx, New York, United States
The Children's Hosp. of Philadelphia
Philadelphia, Pennsylvania, United States
Countries
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Related Links
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Website for the Adolescent Trials Network for HIV/AIDS Interventions
Other Identifiers
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ATN 053
Identifier Type: -
Identifier Source: org_study_id
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