Health TrialsbyHealthPanel

Disseminating Effective Sexual Health Programs in Schools Using iCHAMPSS

ConditionSexual Health Education
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorThe University of Texas Health Science Center, Houston

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Licensed educator or administrator who holds one of the following positions: 1) district or school administrator (e.g., health coordinators, instructional specialists, and curriculum coordinators), 2) health and physical education teachers, and 3) social and health service staff (e.g., nurses and counselors) in a Texas school district participating in the iCHAMPSS 2.0 study

Disqualifiers

not holding a job in a Texas school district as a school stakeholder, OR holding a job in a Texas school district as a school stakeholder but not in a school district participating in the iCHAMPSS 2.0 study

Trial design

Design model

Crossover

Treatments tested in this trial

  • iCHAMPSS 2.0

    Behavioral

    iCHAMPSS 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)

Treatment groups

75 Participants
are divided into 3 treatment groups
Group A: Arm 1: 1 semester of implementation then 7 semesters of interventionExperimental treatment 1 intervention
Group B: Arm 2: 1 semester of control, 1 semester of implementation then 7 semesters of interventionExperimental treatment 1 intervention
Group C: Arm 3: 1 semesters of control, 1 semester of implementation then 6 semesters of interventionExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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)
2

Rate of implementation of the EBP

Time frame
From baseline to end of intervention period (about 20 to 30 months from baseline)

Secondary outcomes

1

Percentage of School Health Advisory Councils (SHACs) that have recommended a sexual health EBP to their school board

Time frame
From baseline to end of intervention period (about 20 to 30 months from baseline)
2

Percentage of School Health Advisory Councils (SHACs) that have adopted a sexual health EBP to their school board

Time frame
From baseline to end of intervention period (about 20 to 30 months from baseline)
3

Percentage of schools with the school board's approval of an Evidence Based Program (EBP)

Time frame
From baseline to end of intervention period (about 20 to 30 months from baseline)
4

Percentage of schools with the principal's approval of an EBP

Time frame
From baseline to end of intervention period (about 20 to 30 months from baseline)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

The University of Texas Health Science Center, Houston

Lead sponsor

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator

Source ClinicalTrials.gov
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