NCT03311061

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,000

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2017

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Completed
Same day until next milestone

Study Start

First participant enrolled

October 10, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 16, 2017

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2020

Completed
Last Updated

October 16, 2017

Status Verified

October 1, 2017

Enrollment Period

3 years

First QC Date

October 10, 2017

Last Update Submit

October 10, 2017

Conditions

Keywords

Teen PregnancyPreventionPositive Youth DevelopmentFinancial LiteracyCollege and Career ReadinessSchool Based InterventionAge 13-19Behavior Modification

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

EXPERIMENTAL

The 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.

Other: DREAMS Curriculum

Non DREAMS

ACTIVE COMPARATOR

The 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.

Other: DREAMS Curriculum

Interventions

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

DREAMSNon DREAMS

Eligibility Criteria

Age13 Years - 19 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

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

Study Sites (1)

Bee Busy Inc.

Houston, Texas, 77036, United States

Location

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

Locations