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Recruiting NCT06581536

NCT06581536 Rigorous Evaluation of Yes and Know, a Fully Virtual Sexual Health and Well-Being Intervention for Youth

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Clinical Trial Summary
NCT ID NCT06581536
Status Recruiting
Phase
Sponsor ETR Associates
Condition Pregnancy Related
Study Type INTERVENTIONAL
Enrollment 1,200 participants
Start Date 2025-08-06
Primary Completion 2027-12-31

Eligibility & Interventions

Sex All sexes
Min Age 14 Years
Max Age 19 Years
Study Type INTERVENTIONAL
Interventions
Yes and Know curriculumNutrition Education for Adolescents

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 1,200 participants in total. It began in 2025-08-06 with a primary completion date of 2027-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study is a 2-arm cluster randomized controlled trial with approximately 1,200 youth aged 14-19 years to assess the effectiveness of Yes and Know, a sexual health education program. To be eligible, participants must be 14-19 years old and English-speaking. Those in the treatment arm will receive Yes and Know, a synchronous virtual program delivered over multiple sessions totaling nine hours, along with asynchronous online activities and resources. Those in the control arm will receive a similarly structured program focused on nutrition education. Participants will complete brief online surveys at baseline and at 3 and 12 months after the synchronous sessions. The study will assess the program's effectiveness in reducing the prevalence of unprotected sex among youth and improving short-term outcomes, such as knowledge of reproductive health and healthy relationships, self-efficacy, and the use of reproductive health services.

Eligibility Criteria

Inclusion Criteria: * Ages 14-19; and * English speaking. Exclusion Criteria: \- Anyone not meeting inclusion criteria.

Contact & Investigator

Central Contact

Rebecca A Braun, DrPH, MPH

✉ rebecca.braun@etr.org

📞 510-858-0989

Principal Investigator

Rebecca A Braun, DrPH, MPH

PRINCIPAL INVESTIGATOR

ETR Associates

Frequently Asked Questions

Who can join the NCT06581536 clinical trial?

This trial is open to participants of all sexes, aged 14 Years or older, up to 19 Years, studying Pregnancy Related. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06581536 currently recruiting?

Yes, NCT06581536 is actively recruiting participants. Contact the research team at rebecca.braun@etr.org for enrollment information.

Where is the NCT06581536 trial being conducted?

This trial is being conducted at Watsonville, United States.

Who is sponsoring the NCT06581536 clinical trial?

NCT06581536 is sponsored by ETR Associates. The principal investigator is Rebecca A Braun, DrPH, MPH at ETR Associates. The trial plans to enroll 1,200 participants.

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