MASH: Evaluation of a Middle School Comprehensive Sexual Health Media Literacy Education Program

Sponsor
Innovation Research & Training (Other)
Overall Status
Completed
CT.gov ID
NCT02359422
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
1,017
1
2
16
63.6

Study Details

Study Description

Brief Summary

The purpose of this study is to conduct a randomized controlled trial of a media literacy education program for middle school students with the goal of enhancing decision-making skills to prevent early and risky sexual behavior and teen pregnancy, and encourage healthy relationships.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Media Aware-Sexual Health
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
1017 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Randomized Control Trial Efficacy Study of a Comprehensive Sexual Health Media Literacy Education Program for Middle School Students
Study Start Date :
Apr 1, 2014
Actual Primary Completion Date :
Aug 1, 2015
Actual Study Completion Date :
Aug 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Media Aware-Sexual Health

10-lesson middle school, comprehensive sexual health program developed based upon the Message Interpretation Processing model designed to increase critical thinking skills about media messages and reduce risky sexual behaviors.

Behavioral: Media Aware-Sexual Health
10-lesson middle school, comprehensive sexual health media literacy education program. Each lesson take approximately 50 minutes to teach and will be taught every school day for 2 weeks.

No Intervention: Wait-list control

Outcome Measures

Primary Outcome Measures

  1. Change in self-reported sexual activity assessed via questionnaire. [2 weeks]

  2. Change in self-reported sexual activity assessed via questionnaire. [3 months]

Secondary Outcome Measures

  1. Change in self-reported intentions to engage in sexual activity assessed via questionnaire. [2 weeks]

  2. Change in self-reported intentions to engage in sexual activity assessed via questionnaire. [3 months]

  3. Change in self-reported attitude toward sexual activity assessed via questionnaire. [2 weeks]

  4. Change in self-reported attitude toward sexual activity assessed via questionnaire. [3 months]

  5. Change in self-reported attitudes toward contraception assessed via questionnaire. [2 weeks]

  6. Change in self-reported attitudes toward contraception assessed via questionnaire. [3 months]

  7. Change in self-reported attitude toward sexual communication assessed via questionnaire. [2 weeks]

  8. Change in self-reported attitude toward sexual communication assessed via questionnaire. [3 months]

  9. Change in self-reported perceived norms regarding sexual activity assessed via questionnaire. [2 weeks]

  10. Change in self-reported perceived norms regarding sexual activity assessed via questionnaire. [3 months]

  11. Change in self-reported perceived norms regarding contraception assessed via questionnaire. [2 weeks]

  12. Change in self-reported perceived norms regarding contraception assessed via questionnaire. [3 months]

  13. Change in self-reported perceived norms regarding sexual communication assessed via questionnaire. [2 weeks]

  14. Change in self-reported perceived norms regarding sexual communication assessed via questionnaire. [3 months]

  15. Change in self-reported self-efficacy to refusal sexual activity assessed via questionnaire. [2 weeks]

  16. Change in self-reported self-efficacy to refusal sexual activity assessed via questionnaire. [3 months]

  17. Change in self-reported self-efficacy to use contraception assessed via questionnaire. [2 weeks]

  18. Change in self-reported self-efficacy to use contraception assessed via questionnaire. [3 months]

  19. Change in self-reported self-efficacy for sexual communication assessed via questionnaire. [2 weeks]

  20. Change in self-reported self-efficacy for sexual communication assessed via questionnaire. [3 months]

  21. Change in self-reported intentions for condom/contraception use assessed via questionnaire. [2 weeks]

  22. Change in self-reported intentions for condom/contraception use assessed via questionnaire. [3 months]

  23. Change in self-reported intentions for sexual communication assessed via questionnaire. [2 weeks]

  24. Change in self-reported intentions for sexual communication assessed via questionnaire. [3 months]

Other Outcome Measures

  1. Change in media deconstruction skills assessed via questionnaire. [2 weeks]

  2. Change in media deconstruction skills assessed via questionnaire. [3 months]

  3. Change in perceived realism of media messages assessed via questionnaire. [2 weeks]

  4. Change in perceived realism of media messages assessed via questionnaire. [3 months]

  5. Change in perceived similarity to media messages assessed via questionnaire. [2 weeks]

  6. Change in perceived similarity to media messages assessed via questionnaire. [3 months]

  7. Change in perceived desirability of media messages assessed via questionnaire. [2 weeks]

  8. Change in perceived desirability of media messages assessed via questionnaire. [3 months]

  9. Change in media skepticism assessed via self-report questionnaire. [2 weeks]

  10. Change in media skepticism assessed via self-report questionnaire. [3 months]

  11. Change in identification to media messages assessed via questionnaire. [2 weeks]

  12. Change in identification to media messages assessed via questionnaire. [3 months]

  13. Change in acceptance of dating violence norms assessed via questionnaire. [2 weeks]

  14. Change in acceptance of dating violence norms assessed via questionnaire. [3 months]

  15. Change in acceptance of gender role norms assessed via questionnaire. [2 weeks]

  16. Change in acceptance of gender role norms assessed via questionnaire. [3 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
10 Years to 15 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Must be able to read and write in English
Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 innovation Research & Training Durham North Carolina United States 27707

Sponsors and Collaborators

  • Innovation Research & Training
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Investigators

  • Principal Investigator: Tracy M Scull, PhD, Innovation Research & Training

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Innovation Research & Training
ClinicalTrials.gov Identifier:
NCT02359422
Other Study ID Numbers:
  • iRT-2R44HD061193-02-RCT
  • 2R44HD061193-02
First Posted:
Feb 10, 2015
Last Update Posted:
Nov 20, 2015
Last Verified:
Nov 1, 2015

Study Results

No Results Posted as of Nov 20, 2015