Feasibility Study of the Online High School Media Aware Program (FS-OHSMAP)

February 25, 2019 updated by: Innovation Research & Training

Web-based High School Media Literacy for Healthy Relationships,

This is a pretest-posttest feasibility study of Media Aware Sexual Health - High School, an interactive web-based comprehensive sexual health media literacy education program for high school students. The program is designed to develop students' critical thinking skills and promote sexual health. It is hypothesized that this program will enhance adolescents' media literacy skills, sexual health knowledge, cognitions (i.e., attitudes, self-efficacy, and norms), and behaviors regarding healthy sexual decision-making.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

367

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • North Carolina
      • Durham, North Carolina, United States, 27707
        • innovation Research & Training

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 17 years (Child)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. Students must be in grades 9 or 10 in participating classrooms at participating schools.
  2. Students must be able to speak and read English because the study materials (e.g., questionnaires) and the program are in English.
  3. Students must have appropriate permissions to receive sex education per school districts' policy (i.e., opt-in policy or opt-out policy).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Media Aware Sexual Health - High School
Students received the web-based Media Aware Sexual Health - High School program.
Media Aware Sexual Health is a web-based comprehensive sexual health education program for high school students that uses a media literacy approach.
Other Names:
  • Media Aware
No Intervention: Typical Health Education Programming
Students received their regular health education programming not related to sexual health education.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in willingness to engage in unprotected sex
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (strongly disagree; disagree; agree; strongly agree) assessing the degree to which one is willing to engage in unprotected sex (Suppose you were with a boyfriend/girlfriend. He/she wants to have sex, but neither of you have any form of protection. In this situation, how willing would you be to go ahead and hook-up anyway?).
pretest and posttest (approximately one week after pretest)
Change in willingness to hook up against own wishes
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (strongly disagree; disagree; agree; strongly agree) assessing the degree to which one is willing to hook up with someone even if they are not sure that they really want to. (Suppose you were with a boyfriend/girlfriend. He/she wants to hook-up, but you are not sure that you want to. In this situation, how willing would you be to go ahead and hook-up anyway?).
pretest and posttest (approximately one week after pretest)
Change in intentions to use contraception/protection
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (not at all likely; unlikely; likely; extremely likely) assessing intentions to use contraception (e.g., if you were to have vaginal or anal sex, how likely would you be to use a condom?).
pretest and posttest (approximately one week after pretest)
Change in intentions to engage in sexual activity
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (not at all likely; unlikely; likely; extremely likely) assessing participants intentions to engage in sex in the next year (How likely is that you will have any type of sexual contact with another person (oral sex, anal sex, vaginal sex, or genital-to-genital contact) in the next year?).
pretest and posttest (approximately one week after pretest)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Efficacy to refuse sexual activity
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (strongly disagree; disagree; agree; strongly agree) assessing participants efficacy to refuse sex (e.g., I could say no to someone who is pressuring me to have sex).
pretest and posttest (approximately one week after pretest)
Efficacy to communicate before sex
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (strongly disagree; disagree; agree; strongly agree) assessing participants efficacy to communicate about sexual health (e.g., I could talk with a boy/girlfriend about using condoms for sexually transmitted infection protection).
pretest and posttest (approximately one week after pretest)
Efficacy to use contraception/protection
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (strongly disagree; disagree; agree; strongly agree) assessing participants efficacy to get and use contraception (e.g., If I wanted to, I could get condoms or another form of contraception).
pretest and posttest (approximately one week after pretest)
Intentions to communicate before sex
Time Frame: pretest and posttest (approximately one week after pretest)
4-point Likert scale (not at all likely; unlikely; likely; extremely likely) assessing intentions to communicate about sexual health before sex (e.g., Before deciding to have sex, how likely would you be to talk to a boy/girlfriend about HIV/AIDS or other sexually transmitted infections?).
pretest and posttest (approximately one week after pretest)
Sexual health knowledge
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked several multiple choice and T/F questions about sexual health.
pretest and posttest (approximately one week after pretest)
Norms - Frequency of teen risky sexual activity (%)
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked to indicate what percentage [0% = no teens; 100% = all teens] are engage in risky sexual activities (e.g., have sex with someone who is much older).
pretest and posttest (approximately one week after pretest)
Norms - teen sexual activity (%)
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked to indicate what percentage [0% = no teens; 100% = all teens] are engage in sexual activity.
pretest and posttest (approximately one week after pretest)
Perceived realism of media messages
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) the degree to which they agreed that teens on the media: 1) do things that average teens do; 2) act like average teens; 3) are as sexually experienced as average teens; 3) get pregnant as often as average teens; 4) get STIs as often as average teens.
pretest and posttest (approximately one week after pretest)
Perceived similarity to media messages
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) the degree to which they agreed that: 1) The things I do in my life are similar to what I see teens do in the media; 2) I look like teens I see in the media; 3) I like the kinds of things that teens in the media like.
pretest and posttest (approximately one week after pretest)
Cognitive elaboration of advertisement
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are shown an advertisement and responded on a 4-point Likert scale (not much at all; a little; a good amount; a lot) the extent to which they: 1) thought about the ad; 2) spent time thinking about the ad; and 3) paid attention to the ad.
pretest and posttest (approximately one week after pretest)
Media Skepticism
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) the degree to which they agree with several statements about media (e.g., Media are dishonest about what happens when people drink alcohol).
pretest and posttest (approximately one week after pretest)
Teen Sex Attitudes
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) the degree to which they agree with several statements about teen sex (e.g., it is ok for teens to be sexually active).
pretest and posttest (approximately one week after pretest)
Risky Teen Sex Attitudes
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) the degree to which they agree with several statements about teens engaging in risky sexually behaviors (e.g., I believe it is ok for teens to do use alcohol or drugs before or during a sexual encounter.)
pretest and posttest (approximately one week after pretest)
Teen Contraception Use Attitudes
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) the degree to which they agree with several statements about teen contraception use (e.g., I believe if a teen is going to have sex, they should always use a condom.)
pretest and posttest (approximately one week after pretest)
Teen Sexual Communication Attitudes
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) the degree to which they agree with several statements about teen sexual communication (e.g., Before deciding to have sex, I believe teens should talk with their parents or another trusted adult).
pretest and posttest (approximately one week after pretest)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Intent to intervene as bystander
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (not likely at all; Unlikely; Likely; Extremely likely) how likely they would be to intervene as a bystander (e.g., Approach a friend if I thought they were in an abusive relationship and let them know that I am here to help)
pretest and posttest (approximately one week after pretest)
Efficacy to intervene as bystander
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked to indicate on a scale on 0 (Can't do) to 100 (Very Certain) their degree of confidence in several behaviors (e.g., I could talk to a friend who I suspected is in an abusive relationship.)
pretest and posttest (approximately one week after pretest)
Belief in rape myths
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) their level of agreement on several items pertaining to myths about rape (e.g., It shouldn't be considered rape if a guy is drunk and didn't realize what he was doing.)
pretest and posttest (approximately one week after pretest)
Acceptance of strict gender role stereotypes
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) their level of agreement on several items pertaining to strict gender role stereotypes (e.g., Raising children is primarily a woman's responsibility).
pretest and posttest (approximately one week after pretest)
Acceptance of dating violence
Time Frame: pretest and posttest (approximately one week after pretest)
Participants are asked on a 4-point Likert scale (strongly disagree; disagree; agree; strongly agree) their level of agreement on several items pertaining to dating violence (e.g., It is okay for people to hit their girlfriends/boyfriends if they did something to make them mad).
pretest and posttest (approximately one week after pretest)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 24, 2018

Primary Completion (Actual)

March 12, 2018

Study Completion (Actual)

March 12, 2018

Study Registration Dates

First Submitted

February 21, 2019

First Submitted That Met QC Criteria

February 25, 2019

First Posted (Actual)

February 26, 2019

Study Record Updates

Last Update Posted (Actual)

February 26, 2019

Last Update Submitted That Met QC Criteria

February 25, 2019

Last Verified

February 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • iRT-Media Aware HS-Phase I

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Sexual Behavior

Clinical Trials on Media Aware Sexual Health - High School

3
Subscribe