Clinical trial Recruiting at 1 site Interventional Ages 18 to 55

Mobile app to deliver CBT-AR for ARFID

Official title: Development and Testing of a Mobile App to Scale Delivery of Cognitive-behavioral Therapy for Avoidant/Restrictive Food Intake Disorder

Run by Massachusetts General Hospital · NCT06898177 · Data updated 2026-11-12

A mobile app is being tested to see if it can deliver cognitive-behavioral therapy for ARFID to adults who have not yet received face-to-face CBT-AR.

Quick facts

Study typeInterventional
Ages18 Years to 55 Years
SexAll
Enrollment60 (estimated)
SponsorMassachusetts General Hospital
Academic / other
Locations1 site (Boston, Massachusetts)
StatusRecruiting
StartedApril 13, 2026
Main results expectedApril 1, 2030
Study endsApril 1, 2030
Registry record updatedJune 16, 2026
Trial IDNCT06898177 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with ARFID who are fluent in English, reside in the United States, have internet access, and have not previously completed face-to-face CBT-AR at MGH.

Probably not a fit

Individuals with medical instability, severe comorbid conditions needing additional treatment, or those unable to use mobile technology may not benefit from this app-based approach.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study tests a mobile app version of CBT-AR to scale access to evidence-based treatment for Avoidant/Restrictive Food Intake Disorder (ARFID). Eligible participants are adults with ARFID who speak English, live in the United States, and have a compatible smartphone with internet access. The trial seeks to determine whether the app can be feasibly used and whether it can deliver helpful therapeutic content for ARFID outside traditional in-person care. Key safety considerations include excluding individuals with significant medical instability, comorbid disorders needing other treatment, or those who have completed face-to-face CBT-AR at MGH. Leader institution is Massachusetts General Hospital, and the study location is in Boston, MA.

Why it matters

Potential benefit: If successful, the app could provide a scalable, inexpensive way to deliver CBT-AR to more people with ARFID.

How similar studies have gone: Previous efforts to adapt CBT for eating disorders into mobile formats have shown promise for accessibility and engagement, but app-based CBT-AR for ARFID is still emerging.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Current avoidant/restrictive food intake disorder based on DSM-5 criteria
2. Must not have completed face-to-face CBT-AR at the Eating Disorders Clinical and Research Program at Massachusetts General Hospital
3. Ability to speak, write, and understand English
4. Residence in the United States
5. Access to an internet-connected smartphone device

Exclusion Criteria:

1. Underweight status (i.e., BMI \< 18.5 kg/m2)
2. Complete lack of oral intake or dependence on supplemental feeding
3. Feeding or eating disorder other than ARFID
4. Any comorbid clinically significant disorder that would require attention beyond the study treatment

6\. Medical instability requiring inpatient care according to the American Psychiatric Association 2023 treatment guidelines for eating disorders 7. Medical history of intellectual disability 8. Illiteracy

Where it's running

  • Massachusetts General Hospital
    Boston, Massachusetts, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.