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A Feasibility Trial of Sisterhood 2.0

A Gender Transformative Program to Prevent Sexual Violence and Relationship Abuse Among Adolescent Women: A Feasibility Trial of Sisterhood 2.0

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04388696
Enrollment
246
Registered
2020-05-14
Start date
2018-12-01
Completion date
2020-01-31
Last updated
2020-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescent Behavior, Communication, Personal, Coping Skills, Emotional Abuse, Group, Peer, Violence, Domestic, Violence in Adolescence, Violence, Non-accidental, Violence, Physical, Violence, Sexual

Brief summary

This pilot quasi-experimental community based trial examines the feasibility of a sexual violence and adolescent relationship abuse prevention program for girls aged 14-19. Feasibility is assessed through participant attendance, retention and program satisfaction measures and interviews are conducted at baseline, end of program and 3 month follow up (endline) about participant experiences.

Detailed description

The goal of the project is to adapt and pilot a gender transformative, sexual violence and adolescent relationship abuse prevention program, Sisterhood 2.0, among African American high school-age females in a community-based setting. The Sisterhood 2.0 curriculum was adapted from Program M, created in 2006 by Promundo to address health and empowerment of young women aged 15-24. The curriculum engages young women in questioning rigid and non-equitable stereotypes about masculinity and femininity and how these rigid stereotypes affect their health and well-being. This study will pilot test, using a quasi-experimental design, the participant satisfaction with the program through measures of attendance and retention, and be compared to a job skills development curriculum. This study is significant because there are too few evidence-based sexual violence and adolescent relationship abuse prevention program in the U.S., none that are specifically tailored for African American adolescent females, and there are no evidence- based programs implemented in community settings that target both sexual violence and adolescent relationship abuse and adolescent sexual health.

Interventions

BEHAVIORALSisterhood 2.0

The Sisterhood 2.0 curriculum was adapted from Program M, created in 2006 by Promundo to address health and empowerment of young women aged 15-24. The curriculum engages young women in questioning rigid and non-equitable stereotypes about masculinity and femininity and how they affect both women's and men's health and well-being.

Sponsors

Department Human Services, Pennsylvania
CollaboratorUNKNOWN
Fisa Foundation
CollaboratorUNKNOWN
The Grable Foundation
CollaboratorUNKNOWN
University of Pittsburgh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The 18-24 hour content (divided into 8, 3 hour sessions) are spread over a 3 week to 2 month period. Sessions explored gender, consider harmful messages around femininity and socially acceptable images of women, healthy sexuality, healthy relationships and connections, understanding and identifying sexual abuse and assault, and self care. Control Program: The control intervention used widely-used curricula focused on job skills development and life skills. Trained prevention educators provided the programs for both intervention and control arms and were trained to implement either the Sisterhood 2.0 program or the job skills curriculum.

Eligibility

Sex/Gender
FEMALE
Age
13 Years to 19 Years
Healthy volunteers
Yes

Inclusion criteria

* Participants must be ages 13-19 (inclusive) * Participants must speak English * Participants must self identify as female

Exclusion criteria

* Not ages 13-19 (inclusive) * Does not speak English * Does not identify as female

Design outcomes

Primary

MeasureTime frameDescription
Participant Attendancethrough study completion, an average of 1 per weekAttendance recorded at beginning and end of each session with a weekly satisfaction survey. Calculated as a proportion of total number of sessions.
Participant Retentionpost-intervention at Week 8At the end of the program, participants were asked why they returned or did not return to the program each week and their reasons for missing any sessions.
Participant Satisfactionthrough study completion, an average of 1 per weekParticipants were asked about how satisfied they were with the topic discussed and format of the program each week.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026