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Evaluation of Curriculum for Teen Pregnancy Prevention: Decisions, Responsibility, Empowerment, Accountability, Motivations & Success

Evaluation of Curriculum for Teen Pregnancy Prevention: Decisions, Responsibility, Empowerment, Accountability, Motivations & Success (DREAMS) in Houston TX

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03311061
Acronym
DREAMS
Enrollment
2000
Registered
2017-10-16
Start date
2017-10-10
Completion date
2020-09-30
Last updated
2017-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Teen Pregnancy

Keywords

Teen Pregnancy, Prevention, Positive Youth Development, Financial Literacy, College and Career Readiness, School Based Intervention, Age 13-19, Behavior Modification

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.

Detailed description

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.

Interventions

OTHERDREAMS Curriculum

Teen Pregnancy Prevention Curriculum as described in arm/group description.

Sponsors

Department of Health and Human Services
CollaboratorFED
Winter Rose Services, LLC
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Masking description

Students are masked through

Intervention model description

Two groups of participants. group A will receive the DREAMS Curriculum intervention. Group B (Control group) will receive curriculum already in place at school.

Eligibility

Sex/Gender
ALL
Age
13 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

Age 13-19; enrolled in participating high school health class; passive consent received;

Exclusion criteria

Students who enrolled in classes post baseline. Students who had previously failed the HS course and was already exposed to DREAMS curriculum.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants who had sex without a condomimmediately post-intervention, 6-months and 12-months-post interventionNumber 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.
Number of participants who ever had seximmediately post-intervention, 6-months and 12-months-post interventionNumber 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.
Number of penile-vaginal sex actsimmediately post-intervention, 6-months and 12-months-post interventionNumber 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.
Number of participants who used other birth control methodsimmediately post-intervention, 6-months and 12-months-post interventionNumber 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.
Number of participants who had an STIimmediately post-intervention, 6-months and 12-months-post interventionNumber 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.
Number of participants who increased knowledge concerning risks associated with unprotected seximmediately post interventionNumber 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.

Secondary

MeasureTime frameDescription
Number of participants (by gender, age, and race/ethnicity) who had had a teenage pregnancy12-months-post interventionNumber of participants (by gender, age, and race/ethnicity) who had had a teenage pregnancy. The relative difference of teenage pregnancies (among genders, ages, and race/ethnicity) in the intervention versus control group at 12-months post-intervention.
Number of participants who had had a teenage pregnancy12-months-post interventionNumber of participants who had had a teenage pregnancy. The relative difference of teenage pregnancies in the intervention versus control group at 12-months post-intervention.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026