Project HOME: Home-Based Treatment Options and Mechanisms for Eating Disorders
Launched by UNIVERSITY OF PITTSBURGH · Dec 21, 2021
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The Project HOME clinical trial is studying two different psychological treatments for adolescents with anorexia nervosa (AN) to see how effective they are when delivered at home. In this trial, 50 adolescents diagnosed with AN and their caregivers will be randomly assigned to one of two treatment options: family-based treatment or integrated family therapy. The goal is to understand how well these treatments work in a real-world setting, especially when they are accessible from home. Participants will share information about their weight, eating habits, and emotional well-being, and their caregivers will help provide feedback on how well the treatment is going.
To be eligible for this trial, participants must meet certain criteria, including having a diagnosis of AN or atypical AN, living at home with supportive caregivers, and being medically stable. This means they need to be at a safe weight and healthy enough to receive outpatient treatment. It’s also important that participants are not currently hospitalized for other health issues or involved in other psychological treatments for eating disorders. If eligible, participants can expect to engage in therapy sessions at home, and their progress will be closely monitored throughout the study. This trial aims to improve understanding of how to make effective eating disorder treatments more accessible and beneficial for young people and their families.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Meets criteria for AN or atypical AN according to DSM-5 diagnostic criteria.
- • Currently living at home with caregivers who are willing to engage in family treatment.
- • Medically stable for outpatient treatment according to the recommended thresholds of the American Academy of Pediatrics and the Society of Adolescent Medicine (e.g., ≥75% of expected body weight, heartrate ≥50 beats per minute) and receiving medical monitoring from a clinician throughout treatment.
- • If on psychotropic medication, meets all eligibility criteria while on stable dose of psychotropic medication for a co-morbid condition.
- • Available for follow-up.
- Exclusion Criteria:
- • Associated physical illness that necessitates hospitalization.
- • Psychotic illness/other mental illness requiring hospitalization.
- • Current dependence on drugs or alcohol.
- • Physical conditions (e.g. diabetes mellitus, pregnancy) known to influence eating or weight.
- • Concurrent involvement in other psychological treatment for an eating disorder.
- • Developmental delay that would preclude participation in the intervention.
About University Of Pittsburgh
The University of Pittsburgh is a leading research institution known for its commitment to advancing medical science and improving patient care through innovative clinical trials. With a robust infrastructure for research and a multidisciplinary approach, the university fosters collaboration among experts in various fields, facilitating the development of novel therapies and interventions. Its clinical trial programs emphasize ethical standards, patient safety, and the integration of cutting-edge technology, making the University of Pittsburgh a pivotal contributor to the landscape of clinical research and a trusted partner in the pursuit of health advancements.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Pittsburgh, Pennsylvania, United States
Pawtucket, Rhode Island, United States
Providence, Rhode Island, United States
Patients applied
Trial Officials
Andrea B Goldschmidt, Ph.D.
Principal Investigator
The University of Pittsburgh
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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