Actively Recruiting

Phase Not Applicable
Age: 14Years - 19Years
All Genders
NCT06581536

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

Led by ETR Associates · Updated on 2026-05-14

1200

Participants Needed

1

Research Sites

125 weeks

Total Duration

On this page

Sponsors

E

ETR Associates

Lead Sponsor

U

University of California, San Francisco

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 14Years - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Ages 14 to 19 years
  • English speaking
Not Eligible

You will not qualify if you...

  • Anyone not meeting the inclusion criteria

AI-Screening

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Trial Site Locations

Total: 1 location

1

ETR Associates

Watsonville, California, United States, 95076

Actively Recruiting

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Research Team

R

Rebecca A Braun, DrPH, MPH

CONTACT

P

Pamela K Anderson, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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