Virtual sexual health and well-being program for youth
Rigorous Evaluation of Yes and Know, a Fully Virtual Intervention Integrating Group-based Education With Digital Tools to Improve Youth Sexual Health and Well-Being
This study is testing a virtual sexual health education program for young people aged 14-19 to see if it helps them learn more and feel more confident about their sexual health compared to a nutrition program.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 1200 (estimated) |
| Ages | 14 Years to 19 Years |
| Sex | All |
| Sponsor | ETR Associates Academic / other |
| Locations | 1 site (Watsonville, California) |
| Trial ID | NCT06581536 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of Yes and Know, a virtual sexual health education program for youth aged 14-19. Participants will be randomly assigned to either the sexual health intervention or a nutrition education program, with both groups receiving nine hours of instruction delivered through synchronous online sessions. The study aims to assess changes in knowledge, self-efficacy, and behaviors related to sexual health over a 12-month period. Participants will complete online surveys at baseline, 3 months, and 12 months to measure outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are English-speaking youth aged 14-19 years.
Not a fit: Patients who do not meet the age or language criteria will not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly reduce unprotected sex among youth and improve their understanding of reproductive health.
How similar studies have performed: Other studies have shown success with similar virtual health education approaches, indicating potential for positive outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Ages 14-19; and * English speaking. Exclusion Criteria: \- Anyone not meeting inclusion criteria.
Where this trial is running
Watsonville, California
- ETR Associates — Watsonville, California, United States (Recruiting)
Study contacts
- Principal investigator: Rebecca A Braun, DrPH, MPH — ETR Associates
- Study coordinator: Rebecca A Braun, DrPH, MPH
- Email: rebecca.braun@etr.org
- Phone: 510-858-0989
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.