Family-based HIV Prevention for Adolescent Females
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 168
- Locations
- 2
- Primary Endpoint
- Test the feasibility of implementing intervention
Study Overview
Brief Summary
This is an exploratory/developmental study to support the early phases of development and evaluation of a family-based HIV prevention program for adolescent girls prior to a full-scale trial. Research on the new intervention will include evaluating the feasibility, tolerability, and acceptability of the intervention, and allow us to obtain the preliminary data needed as a pre-requisite to a larger-scale intervention study.
Adolescent females and their mother/guardian will be randomized to either: a family-based risk reduction intervention; or a no-treatment control group condition. Participants in both conditions will be assessed at baseline, immediate post-intervention, and at 3- and 6-month follow-ups. A subset of families (12 adolescents and 12 mothers) will participate in a qualitative interview following the 6-month follow-up, in which information will be obtained on participant perception of procedures and intervention content, and whether they have utilized skills taught following the end of the project.
Detailed Description
Participants will be involved with the study and follow up for a total of 32 to 36 weeks.
68-84 female adolescents and their mother/guardian (total N = 136-168).
African American or mixed race, sexually active female adolescents age 15 to 19 who are at risk for HIV infection and their mother/guardian
The adolescent participant and her mother/guardian will be randomized to either a family-based risk reduction intervention or a no-treatment control group condition.
Participants in both conditions will be assessed at baseline, immediate post-intervention, and at 3- and 6-month follow-ups. A subset of 24 participants from the intervention condition (12 adolescents and 12 mothers) will participate in a qualitative interview following the 6-month follow-up, in which information will be obtained on participant perception of procedures and intervention content, and whether they have utilized skills taught following the end of the project.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Triple (Participant, Care Provider, Investigator)
Eligibility Criteria
- Ages
- 15 Years to 19 Years (Child, Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Between the age of 15 years and 0 days and 19 years and 364 days at the time of initial eligibility screening.
- •Born in the United States
- •Self identifies as all or part African American.
- •Sexually active, defined as having had vaginal or anal intercourse
- •Has engaged in unprotected sex during the past 3 months
- •Is willing to invite and participate with her mother/guardian in the intervention
- •Has either a biological mother or a guardian who is willing to participate in the study and meets the eligibility criteria
- •For the purposes of this pilot study, biological mothers are eligible, as are non-biological primary caretakers serving as mother/guardians who have guardianship of the adolescent and with whom the adolescent is living.
- •Able to understand spoken and written English sufficiently to provide assent/consent and to be interviewed and participate in the study intervention.
- •Not intending to relocate out of the current geographical area for the duration of study participation.
- •Provides informed assent or consent
- •Mother or Mother/guardian
- •Has legal guardianship; and
- •Currently resides with the adolescent.
- •Self identifies as all or part African American.
- •Born in the United States
- •Able to understand spoken and written English sufficiently to provide consent and to be interviewed and participate in the study intervention.
- •Not intending to relocate out of the current geographical area for the duration of study participation.
- •Provides informed consent
Exclusion Criteria
- •Adolescent is currently pregnant or has carried a pregnancy to term
- •Adolescent self-reports as HIV positive
Arms & Interventions
Family-Based Risk Reduction Intervention
The intervention will be delivered in five, two-hour, small group sessions, across five weeks (group will meet once per week). Each of the 5 modules consists of 3 sessions: a one-hour session for the daughters meeting together with each other, a one-hour session for the mothers meeting together with each other; and a one-hour session in which the daughters and mothers meet together. Therefore, each week, the daughters will meet as a group for one hour of each module, while the mothers meet as a group for one hour, and for one hour the mothers and daughters will all meet together.
Intervention: Family-Based Risk Reduction Intervention (Behavioral)
No Treatment Control Group Condition
A no treatment control group condition will be utilized for this preliminary feasibility study. Participants in this condition, both mothers and adolescents will be assessed at baseline, immediate post-intervention, at 3-month follow-up and at 6-month follow-up.
Outcomes
Primary Outcomes
Test the feasibility of implementing intervention
Time Frame: 32-26 Weeks
The primary objective of this pilot study is to test the feasibility of implementing a mother-daughter HIV risk reduction intervention for at-risk female adolescents.
Secondary Outcomes
- Conduct a preliminary efficacy test of the intervention(32-36 Weeks)