Families Moving Forward (FMF) Connect Pro for Mental Health Providers (NCT05960461)
🩺 Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to test a new provider-assisted version of the caregiver Families Moving Forward (FMF) Connect app ("FMF Connect Pro") with mental health providers in the United States. In FMF Connect Pro, mental health providers learn to do routine screening for prenatal alcohol exposure, diagnose fetal alcohol spectrum disorders (FASD), and support families in using the FMF Connect caregiver app. Two different training methods will be compared with a waitlist group in this study. The first training method involves 13-sessions of tele-mentoring using an Extension of Community Healthcare Outcomes (ECHO) approach. The second training method involves a self-directed approach in which providers will access similar content in any asynchronous format on a website. The main questions this study aims to answer are: * What is the proportion of agencies and providers who accept and participate in the clinical trial (Reach)? * Do study groups differ on provider outcome measures of Effectiveness (clients screened/diagnosed), Adoption (provider change in knowledge, self-efficacy), Implementation (practice change, FMF Connect Pro Dashboard usage), and Maintenance of FASD-informed care practice change? All mental health providers in the study will complete online assessments at study entry, 6 months, and 12 months.
Who can join: Review the eligibility criteria below.
Location: Mt. Hope Family Center — Rochester, New York
Age range: 18 Years
🧪 Interventions in This Study
- FMF (Families Moving Forward) Connect Pro (BEHAVIORAL)
- ECHO (Extension of Community Healthcare Outcomes) implementation. (BEHAVIORAL)
- Self-Directed Learning implementation. (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Mt. Hope Family Center — Rochester, New York
📞 Contact the Study Coordinator
Phone: (585) 275-2991
Email: christie_petrenko@urmc.rochester.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Fetal Alcohol Spectrum Disorders
- Choline Supplementation as a Neurodevelopmental Intervention in Fetal Alcohol Spectrum Disorders Study — Minneapolis, Minnesota
- Thrive Person-Centered Planning Program for Young Adults With Fetal Alcohol Spectrum Disorders — Rochester, New York
- My Health Coach App RCT — Rochester, New York
- The Synchrony Study: Examining Music Training for Children With FASD — Albuquerque, New Mexico
- Trigeminal Nerve Stimulation for Children With Prenatal Alcohol Exposure — Los Angeles, California
Explore by condition: All Fetal Alcohol Spectrum Disorders clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.