CompletedNot Applicable

Study of Long-term Efficacy and Mechanisms Underlying the Impact of a Web-based Sexual and Relationship Health Promotion Program With Young Adult Community College Students

United States2,184 participantsStarted 2021-07-21

Plain-language summary

Community college students are an underserved and at-risk population in terms of their sexual and relationship health. This is a three-arm randomized control trial to evaluate the long-term efficacy of a web-based sexual and relationship health promotion program among U.S. community college students (expected N = 2010) and explore the mechanisms underlying the program efficacy.

Who can participate

Age range

18 Years – 19 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Students must be 18 or 19 years of age. * Students must attend one of the community colleges from which this study is recruiting participants. * Students must have an email address to receive study communication. * Students must have access to a computer, tablet, or phone device with internet access as the questionnaires and programs are web-based. * Students must be able to speak and read English because the study materials (e.g., questionnaires, programs) are in English. Exclusion Criteria: \-

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Relationship Satisfaction

Timeframe: posttest (4-weeks after pretest)

Relationship Satisfaction

Timeframe: 6-month follow-up

Relationship Satisfaction

Timeframe: 12-month follow-up

Percentage of Participants With Relationship Violence Perpetration

Timeframe: posttest (4-weeks after pretest)

Percentage of Participants With Relationship Violence Perpetration

Timeframe: 6-month follow-up

Percentage of Participants With Relationship Violence Perpetration

Timeframe: 12-month follow-up

Percentage of Participants With Relationship Violence Victimization

Timeframe: posttest (4-weeks after pretest)

Trial details

NCT IDNCT04950686

SponsorInnovation Research & Training

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-03-24

Results submitted2025-05-08

View on ClinicalTrials.gov More Sexual Behavior trials

Plain-language summary

Who can participate

Age range

18 Years – 19 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Relationship Satisfaction

Timeframe: posttest (4-weeks after pretest)

Relationship Satisfaction

Timeframe: 6-month follow-up

Relationship Satisfaction

Timeframe: 12-month follow-up

Percentage of Participants With Relationship Violence Perpetration

Timeframe: posttest (4-weeks after pretest)

Percentage of Participants With Relationship Violence Perpetration

Timeframe: 6-month follow-up

Percentage of Participants With Relationship Violence Perpetration

Timeframe: 12-month follow-up

Percentage of Participants With Relationship Violence Victimization

Timeframe: posttest (4-weeks after pretest)