Neuroscience-informed Treatment to Remotely Target Reward Mechanisms in Post-acute Anorexia Nervosa (NCT05799872)
๐ฉบ Plain-English Summary (8th-Grade Level)
The investigators will recruit individuals with broadly-defined AN (n = 80) who are currently in or have recently participated in higher-level eating disorder treatment (e.g., residential, partial hospitalization/day treatment, intensive outpatient treatment). Interested participants will sign consent, complete eligibility assessments, and will be randomized to receive Positive Affect Treatment for Anorexia Nervosa (PAT-AN) or Psychoeducation and Behavioral Therapy (PBT) through teletherapy shortly following discharge from higher level of care. Participants can participate in most other forms of outpatient treatment while receiving the research intervention. Participants will engage in 24 weeks of PAT-AN or PBT starting in the first 3 months post-discharge. At each session, the investigators will complete brief measures assessing treatment acceptability, affect, and eating disorder symptoms. Participants will also complete an assessment battery of self-report, EMA, and neurocognitive measures evaluating primary outcomes (BMI; eating disorder symptoms), secondary outcomes (depression, anxiety, and suicidality), and presumed treatment mechanisms at baseline, end of treatment (EOT), and 3-month follow-up (FU). All assessments will be remotely delivered via HIPAA-compliant platforms.
Who can join: Review the eligibility criteria below.
Location: Virginia Commonwealth University โ Richmond, Virginia
Age range: 18 Years
๐งช Interventions in This Study
- Positive Affect Treatment for Anorexia Nervosa (PAT-AN): (BEHAVIORAL)
- Psychoeducational and Behavioral Therapy (PBT) (BEHAVIORAL)
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (1 Sites)
- Virginia Commonwealth University โ Richmond, Virginia
๐ Contact the Study Coordinator
Phone: (804) 828-2658
Email: venableskg@vcu.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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 ยง 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 Anorexia Nervosa
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- Identifying Networks Underlying Compulsivity in Anorexia Nervosa for Targeting With Neuromodulation โ San Francisco, California
- Investigation of Multi-Family Therapy for Anorexia Nervosa โ Chicago, Illinois
- Appetitive Conditioning in Anorexia Nervosa โ Toronto, Ontario
- Incorporating Narrative Into the Treatment of Youth With Anorexia Nervosa (Virtual) โ San Francisco, California
Explore by condition: All Anorexia Nervosa clinical trials
๐ก 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.