- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03765255
Personal Responsibility Education Program Innovative Strategies: Digital Initiative for Youth (PREIS)
Personal Responsibility Education Program Innovative Strategies: Digital Initiative for Youth; An Innovative Youth-Centered Initiative to Improve the Sexual Health and Socio-Economic Well-Being of Youth in Fresno County, California
Study Overview
Status
Intervention / Treatment
Detailed Description
The Digital Initiative for Youth (DIY) is an innovative, youth-centered, digital intervention that aims to improve the health and well-being of adolescents ages 13-19 in Fresno County, California. In particular, it will address the needs of homeless and unstably housed youth, youth of color, sexual minority youth, and Native American youth using a trauma-informed approach and positive youth development framework.
DIY combines existing, in-person, group-based, comprehensive sexual health education with an app designed in consultation with youth. DIY is built on three strategies: positive youth development, youth-centered design, and wraparound technologies. It will focus on four main areas: sexual health and contraceptive use, healthy relationships, educational and career development, and life skills. The intervention includes six hours of in-person education and an app that includes a resource locator, goal setting, text message reminders, and additional information and referrals.
This study is funded through the Personal Responsibility Education Program Innovative Strategies (PREIS), which is administered by the Family and Youth Services Bureau, part of Health and Human Services,
Fresno EOC is responsible for site and participant recruitment as well as the implementation of the intervention. Participants are randomized at the cohort (group) level. All control group participants will be invited to participate after completion of the long-term follow up period.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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California
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Fresno, California, United States, 93701
- Fresno Economic Opportunities Commission
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Speak/understand Spanish or English
- Live within Fresno County, California at baseline (may move out afterward)
- Age between 13-19
- Have access to a smart phone or internet (does not need to own)
Exclusion Criteria:
- Do not live in Fresno County, California at baseline
- Do not speak or understand Spanish or English
- Severe mental health issues that prevent them from participating
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: In the Know (ITK): sexual health education
Cohorts/participants in the experimental (treatment) arm receive an intervention that combines 6 hours of in-person sexual health and adolescent development education with an app that includes a resource locator, text message reminders (for one month), goal setting, and other resources.
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The in-person sessions include modules on: sexual and reproductive health (2 hours - anatomy, gender and sexual orientation, pregnancy, contraception, sexually transmitted infections); healthy relationships and life skills (2 hours - communication and negotiation, consent, violence, online dating, goal setting, strengths); and educational and career success (2 hours - educational and career options, applying for scholarships and financial aid, job readiness, resume preparation, interview skills).
The app includes: online referrals, personal life plans/goal setting, text message reminders, quizzes, and other resources.
|
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No Intervention: Control: do not receive ITK intervention
Cohorts/participants in the no intervention arm do not receive either the in-person education or the app.
However, after completing the 10 month survey, they will have access to the app and will be invited to participate in the in-person program after the study implementation phase is completed (years 4 and 5).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-reported condom/contraceptive use or no sex in the last three months on survey
Time Frame: Short term follow up (3 months)
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Answered some or all of the time to: In the past 3 months, how often did you or a partner use birth control when you had vaginal sex OR In the past 3 months, how often did you use condoms when you had anal sex?
Respondents complete computer-based survey.
Survey developed by University of California, San Francisco (UCSF).
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Short term follow up (3 months)
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Self-reported use of any clinic services in the last three months on survey
Time Frame: Long-term follow up (9 months)
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Checked any services from survey list after question, "Please check all of the services you have received from a doctor, counselor, therapist, social worker, or clinic in the past 3 months."
Respondents complete computer-based survey.
Survey developed by UCSF.
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Long-term follow up (9 months)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-reported sexual risk behavior on survey
Time Frame: Short-term follow up (3 months)
|
Respondents provide number of sexual partners in past 3 months on computer-based survey.
Survey developed by UCSF.
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Short-term follow up (3 months)
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Self-reported knowledge of local clinical services on survey
Time Frame: Short-term follow up (3 months)
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Answered yes to question on computer-based survey: "Have you heard of a clinic or doctor in your community where teens can get sexual health information and services such as condoms, birth control, pregnancy tests, sexually transmitted infection (STI) tests/treatment, and/or HIV tests?"
Survey developed by UCSF.
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Short-term follow up (3 months)
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-reported healthy relationship skills on survey
Time Frame: Short-term follow up (3 months)
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Increased number of correct answers on knowledge about healthy relationships questions on computer-based survey between baseline and short-term follow up.
Survey developed by UCSF.
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Short-term follow up (3 months)
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Self-reported career and education skills on survey
Time Frame: Long-term follow up (9 months)
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Respondents answer they are or have been enrolled in career training, internships, or educational support.
Respondents complete computer-based survey.
Survey developed by UCSF.
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Long-term follow up (9 months)
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Self-reported goal setting skills on survey
Time Frame: Short-term follow up (3 months)
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Aggregate responses to "worked on an educational and/or career goal" and "made plans to reach your goals" on computer-based survey.
Survey developed by UCSF.
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Short-term follow up (3 months)
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Mara J Decker, DrPH, University of California, San Francisco
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 90AP2688
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- ICF
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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