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Efficacy of a Phone-based Relapse Prevention for Anorexia Nervosa After a First Hospitalization

Efficacy of a Phone-based Relapse Prevention for Anorexia Nervosa After a First Hospitalization

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04102475
Acronym
EATLINE
Enrollment
19
Registered
2019-09-25
Start date
2021-03-18
Completion date
2025-03-08
Last updated
2026-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anorexia Nervosa

Brief summary

Anorexia Nervosa (AN) is a highly challenging disease which consequences are serious. Relapse rate is estimated between 38 and 41% during the year following hospitalization. The efficacy of patients' phone contact procedure on relapse has been assessed and has shown interest in numerous disorders. However, no study has ever used phone contact as a relapse prevention intervention tool in AN. Objective: To evaluate efficacy of a phone contact procedure to increase body weight at 12 months after a first hospitalization for AN, by comparison to standard medical follow-up. Secondary objectives are to evaluate effect of phone contact procedure on: change in body weight at 6 month, general psychopathology disorder, psychopathology disorder specific to AN, rate of usual follow-up visit, and medico-economic impact. Method: Prospective, multicenter, open-label, randomized controlled clinical trial, for subject over 15 years old presenting with diagnosis of AN. Patients randomized in EATLINE group will be contacted by phone at 15 days, 1, 2, 4 and 9 months after discharge from hospitalization. Patients in control group will benefit from usual follow-up. Expected outcomes and perspectives:that there will be a significant decrease in relapse due to phone contact procedure compared to control group. Results would justify additional devices at the end of hospitalization, until development of various connected tools allowing to "stay in contact" with patients in order to optimize the current therapeutic possibilities of AN.

Interventions

OTHEREatline

After discharge from a first hospitalization: Phone calls at 15 days, 1, 2, 4 and 9 months by a trained psychologist. The phone interview will be guided by the same standardized frame, which was developed by a group of experts and tested with a group of patients. The purpose of this intervention is to provide a therapeutic and motivational approach, with positive reinforcement and reassurance. * Added to treatment as usual (TAU): outpatient visits (at least monthly consultations) or scheduled hospitalizations * 6- and 12-month assessments as an outpatient interview with an assessor who is blind to condition

OTHERControl

After discharge from the first hospitalization: * No specific phone calls * TAU: outpatient visits (at least monthly consultations) or scheduled hospitalizations * 6- and 12-month assessments as an outpatient interview with an assessor who is blind to condition

Sponsors

University Hospital, Lille
Lead SponsorOTHER
Ministry of Health, France
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subject over 15 years of age * Diagnosis of AN (restrictive and/or purgative) according to DSM-5 criteria * Included after a first inpatient hospitalization in specialized care * Providing informed, dated and signed consent (for a minor, consent must be signed by both parents who have parental authority ) * With medical insurance * Can be reached by telephone

Exclusion criteria

* Uncompensated psychiatric pathology * Refusal to participate in the study * The inability to consent to care (patient or his/her legal representative) * Pregnancy * Major incapable subject or under guardianship or judicial protection * Homelessness * No mastery of reading and writing

Design outcomes

Primary

MeasureTime frame
change in body mass index (BMI)from discharge of the first hospitalization to 12 months.

Secondary

MeasureTime frame
change in BMI from the first hospitalizationfrom the first hospitalization to 6 months and at 1 year
Mini International Neuropsychiatric Interview (MINI)at baseline, at 6 months , at 1 year
SCID-2 (Structured Clinical Interview for DSM IV Axis II Personality Disorders)at baseline, at 6 months , at 1 year
The level of psychopathology specific to AN assessed by EDI (Eating Disorders Inventory)at baseline, at 6 months , at 1 year
The level of psychopathology specific to AN assessed BSQ (Body Shape Questionnaire)at baseline, at 6 months , at 1 year
The level of psychopathology specific to AN assessed by WCS (Weight and Shape Concern Scale)at baseline, at 6 months , at 1 year
Rate of patients lost to follow-up visitsduring the one year
Rate of patients with at least one re-hospitalization or earlier consultations than expectedduring the one year
Medico-economic evaluation with the MEDEC questionnaireat 6 months, at 1 year

Countries

France

Contacts

PRINCIPAL_INVESTIGATOROlivier Cottencin, MD,PhD

University Hospital, Lille

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 25, 2026