- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02831413
Testing the Effectiveness of Relationship Smarts and the Effects of Enhanced Facilitator Training
May 13, 2019 updated by: Mathematica Policy Research, Inc.
Testing the Effectiveness of Relationship Smarts Curriculum and the Effects of Enhanced Facilitator Training
This project will test the effectiveness of offering healthy marriage and relation education for youth as part of the regular school curriculum and examine whether providing enhanced training and support for facilitators shows promise for enhancing the effects on high school students.
The evaluation will examine a range of students' relationship outcomes, including their attitudes toward relationships, their knowledge of healthy relationships, their communication skills, and the characteristics of their current relationship.
Study Overview
Status
Withdrawn
Intervention / Treatment
Detailed Description
Family Bridges will deliver the "Relationship Smarts +" program to students at 10 Chicago-area high schools.
The RS+ curriculum will be delivered to 9th grade students in the target schools and classrooms during the 2016-2017 and 2017-2018 school years.
The curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week.The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.
Using a three-arm randomized controlled trial design, this study will test the effectiveness of offering RS+ as part of the regular school curriculum on the students' knowledge of healthy relationships, their communication skills, and the characteristics of their current relationship.
In addition to testing the effects of the curriculum, the study will also test the effects of providing enhanced training and support to facilitators.
Study Type
Interventional
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Illinois
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Oak Park, Illinois, United States, 60302
- Family Bridges, Inc.
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
No older than 17 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Students must be age 17 or younger
- have consent from a parent or guardian for evaluation activities
- provide assent for evaluation activities.
Exclusion Criteria:
- Students in evaluation classrooms who do not meet these criteria will still receive programming, but will not be included in the STREAMS data collection activities or in the study's analysis.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: Control
Control group members will receive an alternate curriculum that is not related to relationship education.
Family Bridges has identified a computer programming curriculum, Codeacademy, that teaches students how to use HTML.
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a computer programming curriculum, Codeacademy, that teaches students how to use HTML.
|
|
Experimental: RS+
The RS+ curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week.
The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.
|
The curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week.
The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.
|
|
Experimental: RS+ with enhanced facilitator support
The RS+ curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week.
The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.
Affiliates assigned to this enhanced treatment group will participate in enhanced facilitator training and support activities.
|
The curriculum's 12 sessions will be delivered over a period of about 12 weeks during the winter quarter, with an average of one session taught per week.
The lessons cover topics such as personal values, the principals of smart relationships, communication and conflict management, and sexual decision making.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge about Healthy Relationships
Time Frame: end of programming (approx. 12 weeks after beginning of programming )
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
end of programming (approx. 12 weeks after beginning of programming )
|
|
Attitudes about Healthy Relationships
Time Frame: end of programming (approx. 12 weeks after beginning of programming )
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
end of programming (approx. 12 weeks after beginning of programming )
|
|
Knowledge about Healthy Relationships
Time Frame: 1 year follow-up
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
1 year follow-up
|
|
Attitudes about Healthy Relationships
Time Frame: 1 year follow-up
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
1 year follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Communications skills
Time Frame: end of programming (approx. 12 weeks after beginning of programming )
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
end of programming (approx. 12 weeks after beginning of programming )
|
|
Characteristics of current romantic relationship
Time Frame: end of programming (approx. 12 weeks after beginning of programming )
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
end of programming (approx. 12 weeks after beginning of programming )
|
|
Communications skills
Time Frame: 1 year follow-up
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
1 year follow-up
|
|
Characteristics of current romantic relationship
Time Frame: 1 year follow-up
|
audio computer-assisted self-administered interviewing (ACASI) software on tablet devices.
|
1 year follow-up
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Diane Paulsell, Mathematica Policy Research
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2016
Primary Completion (Actual)
January 1, 2018
Study Completion (Actual)
January 1, 2018
Study Registration Dates
First Submitted
June 2, 2016
First Submitted That Met QC Criteria
July 8, 2016
First Posted (Estimate)
July 13, 2016
Study Record Updates
Last Update Posted (Actual)
May 15, 2019
Last Update Submitted That Met QC Criteria
May 13, 2019
Last Verified
May 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- MPR-500098-FB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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