Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Systematic early support to keep adults with eating disorders engaged in care

Official title: Study of the Effectiveness of a Systematic Minimal Early Intervention on Care Engagement in Adults With Eating Disorders Requesting Specialized Treatment: A Monocentric Pilot Study.

Run by Centre Hospitalier St Anne · NCT07411807 · Data updated 2026-11-12

This pilot tests whether three brief scheduled phone calls and five online support group sessions help adults with anorexia or bulimia stay connected and start specialized treatment after they request care.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment215 (estimated)
SponsorCentre Hospitalier St Anne
Academic / other
Locations1 site (Paris)
StatusRecruiting
StartedDecember 29, 2025
Main results expectedApril 2027
Study endsApril 2027
Registry record updatedFebruary 17, 2026
Trial IDNCT07411807 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) living in Île-de-France who have submitted a request for specialized care at the CMME for anorexia nervosa or bulimia nervosa and who can communicate by phone in French are the intended participants.

Probably not a fit

Patients with BMI >30 kg/m², those already in specialized eating-disorder care, individuals with major hearing/communication barriers in French, or patients under legal protection are unlikely to benefit or are excluded from this intervention.

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

What this trial studies

Eating disorders such as anorexia nervosa and bulimia nervosa often lead to long delays or loss to follow-up before specialized care begins. This monocentric, low-risk interventional pilot at the CMME (GHU Paris Psychiatrie & Neurosciences) offers a minimal early intervention consisting of three structured telephone contacts (around days 7, 45 and 90 after request validation) and five online support group sessions during the waiting period. The study will compare care engagement outcomes to determine whether this package reduces the proportion of patients who are lost before starting treatment and will measure acceptability of the approach. Eligible participants are adults (≥18) residing in Île-de-France who have requested specialized eating-disorder care and can communicate by telephone in French.

Why it matters

Potential benefit: If successful, the intervention could reduce dropouts during the waiting period and increase the number of patients who actually begin specialized eating-disorder treatment.

How similar studies have gone: Brief contact and guided-support interventions have shown promise in reducing attrition in other mental-health services, but targeted early-contact programs specifically for eating disorders are limited and not widely validated.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Individual who has submitted a request for care to the CMME for an eating disorder (anorexia nervosa or bulimia)
* Adult (18 years or older) Resident of the Île-de-France region

Exclusion Criteria:

* Body mass index (BMI) greater than 30 kg/m²: these patients will be directed, from the first telephone contact, to structures or care networks that can offer appropriate treatment.

Poor understanding of the French language

Sensory impairment significantly affecting telephone communication

Patient currently receiving care at a specialized eating disorder facility at the time of the call

Patient not consenting to participate in the study

Subject under legal protection measures (guardianship or curatorship)

Where it's running

  • GHU Paris Psychiatrie et Neurosciences
    Paris, France
    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.