Evaluation of Curriculum for Teen Pregnancy Prevention: Decisions, Responsibility, Empowerment, Accountability, Motivations & Success
DREAMS
1 other identifier
interventional
2,000
1 country
1
Brief Summary
The study is a an evaluation of the teen pregnancy prevention curriculum Decisions, Responsibility, Empowerment, Accountability, Motivations \& Success (DREAMS) through a random control trial. The evaluation will take place in high schools in the greater Houston area. Five cohorts of two classes each in ten HS schools will be used. Randomization will occur each semester for five semesters. Curriculum is ten modules in length delivered in 45 minute classes twice a week for five weeks.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2017
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 10, 2017
CompletedStudy Start
First participant enrolled
October 10, 2017
CompletedFirst Posted
Study publicly available on registry
October 16, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2020
CompletedOctober 16, 2017
October 1, 2017
3 years
October 10, 2017
October 10, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Number of participants who had sex without a condom
Number of participants who had sex without a condom. The relative difference of condom usage during penile-vaginal sex acts in the intervention versus control group at post-intervention, 6-months and 12-months post-intervention.
immediately post-intervention, 6-months and 12-months-post intervention
Number of participants who ever had sex
Number of participants who ever had sex. The relative difference of ever having sex (penile-vaginal sex acts) in the intervention versus control group at post-intervention, 6-months and 12-months post-intervention.
immediately post-intervention, 6-months and 12-months-post intervention
Number of penile-vaginal sex acts
Number of penile-vaginal sex acts. The relative difference of the number of penile-vaginal sex acts in the intervention versus control group at post-intervention, 6-months and 12-months post-intervention.
immediately post-intervention, 6-months and 12-months-post intervention
Number of participants who used other birth control methods
Number of participants who used other birth control methods. The relative difference of birth control methods (e.g., the pill, the patch) during penile-vaginal sex acts in the intervention versus control group at post-intervention, 6-months and 12-months post-intervention.
immediately post-intervention, 6-months and 12-months-post intervention
Number of participants who had an STI
Number of participants who had an STI. The relative difference of reported STI in the intervention versus control group at post-intervention, 6-months and 12-months post-intervention.
immediately post-intervention, 6-months and 12-months-post intervention
Number of participants who increased knowledge concerning risks associated with unprotected sex
Number of participants who increased knowledge concerning risks associated with unprotected sex. The relative difference of knowledge gained in the intervention versus control group at immediately post-intervention.
immediately post intervention
Secondary Outcomes (2)
Number of participants (by gender, age, and race/ethnicity) who had had a teenage pregnancy
12-months-post intervention
Number of participants who had had a teenage pregnancy
12-months-post intervention
Study Arms (2)
DREAMS
EXPERIMENTALThe experimental group will be exposed to the DREAMS curriculum including the supplemental technology based application.It is composed of 10 modules: Introduction; Self Exploration; Healthy Relationships; Adolescent Sexuality; Attitudes and Adolescent Sexual Activity; Consequences of Sex - HIV/STI; Consequences of Sex - Pregnancy; Managing Pressure to Engage in Sexual Activity through the Lens of Social Media; Financial Literacy; Careers; Post secondary Education; Wrap up and Close Out. The technology app will include curriculum support and additional resources. Students will have access to the mobile app after the in school programming ends. The intent is for students to have access to portions of the app that deal with self developed goals and progress monitoring for goals, and resource material. This is similar to a student having continued access to a textbook/other class materials.
Non DREAMS
ACTIVE COMPARATORThe control group experience will include health curriculum already adopted by the school district. Continued services as usual. The control group schools, for the most part, lack any formal pregnancy prevention services. All schools claim that lessons developed by the teachers meet the Texas Essential Knowledge Standards (TEKS). No outside services are provided to students and school based services are limited. The services offered at the schools is predominately abstinence based. Students attending the schools would need to initiate any services that are available within the community. The control group will not have access to the DREAMS curriculum or the technology-based application to enhance the DREAMS curriculum. The technology-based application will be a closed, password protected, system during the research trial.
Interventions
Teen Pregnancy Prevention Curriculum as described in arm/group description.
Eligibility Criteria
You may qualify if:
- Age 13-19; enrolled in participating high school health class; passive consent received;
You may not qualify if:
- Students who enrolled in classes post baseline. Students who had previously failed the HS course and was already exposed to DREAMS curriculum.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Winter Rose Services, LLClead
- Department of Health and Human Servicescollaborator
Study Sites (1)
Bee Busy Inc.
Houston, Texas, 77036, United States
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Students are masked through
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- CEO
Study Record Dates
First Submitted
October 10, 2017
First Posted
October 16, 2017
Study Start
October 10, 2017
Primary Completion
September 30, 2020
Study Completion
September 30, 2020
Last Updated
October 16, 2017
Record last verified: 2017-10