Disseminating Effective Sexual Health Programs in Schools Using iCHAMPSS
Part of paid clinical trials in Houston, Texas.
- Sponsor
- The University of Texas Health Science Center, Houston
- Study ID
- NCT07679620
- Status
- Recruiting
Conditions
- Sexual Health Education
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - N/A
- Healthy Volunteers
- Accepted
Interventions
- iCHAMPSS 2.0 — BEHAVIORALiCHAMPSS 2.0 is designed for Program Champions, critical to EBP use, such as district and school administrators, SHAC members (which include parents), and health and physical education teachers, who are highly motivated to promote sexual health education. iCHAMPSS 2.0 has four features: 1. the CHAMPSS Model tutorial, which familiarizes Champions with the iCHAMPSS 2.0 system 2. a Staging Tool, which helps Champions understand their school's level of readiness to adopt, implement, and maintain a sexual health EBP, and can tailor their experience 3. a tools library, which includes a suite of over 60 decision support tools 4. an interactive linkage system, which is an online platform to help Champions connect with others and to receive technical assistance (TA)
Study Details
The purpose of this study is to assess the efficacy of iCHAMPSS 2.0 in impacting Reach Effectiveness Adoption Implementation Maintenance (RE-AIM) implementation outcomes, with implementation of a sexual health evidence-based program (EBP) assess iCHAMPSS 2.0's efficacy in impacting determinants of sexual health EBP implementation and to conduct a process evaluation to monitor iCHAMPSS 2.0 implementation, reach, dosage, and barriers and facilitators to implementing iCHAMPSS 2.0 during the study.
Key Dates
- Start date
- Apr 2, 2026
- Status verified
- Apr 2026
- Primary completion
- Apr 1, 2028
- Completion
- Apr 1, 2028
Study Design
- Enrollment
- 75 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- PREVENTION
Arms
- Experimental: Arm 1: 1 semester of implementation then 7 semesters of intervention
- Experimental: Arm 2: 1 semester of control, 1 semester of implementation then 7 semesters of intervention
- Experimental: Arm 3: 1 semesters of control, 1 semester of implementation then 6 semesters of intervention
Primary Outcome Measure
Change in percentage of schools within a district implementing an EBP [ Time Frame: From baseline to end of intervention period (about 20 to 30 months from baseline) ]
Central Contacts
- Belinda Hernandez, PhD, MPH(210) 276-9009
- Laura Thormaehlen(713) 500-9000
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The University of Texas Health Science Center at Houston | Houston | Texas | 77030 |