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Web-Based Health Promotion for Sexual Health Education
Study Summary
This trial will evaluate the effectiveness of a web-based sexual and relationship health promotion program for community college students.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I am 18 or 19 years old.I have an email address for study updates.
- Group 1: Delayed Intervention Control
- Group 2: Intervention - Media Aware for Young Adults
- Group 3: Active Control - Health Aware for Young Adults
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Who qualifies to join this clinical trial?
"This medical trial seeks to include 2010 young adults aged 18 or 19 who have suffered sexual assault. To be considered, applicants must possess a device connected to the internet, attend one of the participating community colleges, and furnish an email address for study communication."
Are there any open enrollment opportunities for the trial at this time?
"As per the clinicaltrials.gov website, this research is currently seeking participants. It was initially posted on July 21st 2021 and had its last update on February 16th 2022."
What is the current patient count for this experiment?
"Affirmative. According to the information published on clinicaltrials.gov, this medical trial is still recruiting patients, having been initially posted on July 21st 2021 and last edited on February 16th 2022. The study requires 2010 individuals from one site for participation."
What are the fundamental goals of this research endeavor?
"A 12-month follow up period will be used to assess the study's primary outcome, which is Relationship satisfaction. Secondary measures include Bystander Efficacy (0-100), Sex Refusal Self-Efficacy (1-4) and Attitudes Toward Unprotected Sex (1-4)."
Does the research protocol for this clinical trial include participants over 30 years of age?
"Eligible participants must be between the ages of majority and 19 years old."
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