Cognitive Remediation Therapy in Anorexia Nervosa (TreCogAM)

January 13, 2017 updated by: Assistance Publique - Hôpitaux de Paris

Cognitive Remediation Therapy Effectiveness in Anorexia Nervosa: a Multicenter Randomized Clinical Study

"Clinicians from the Maudsley (IoP, London, UK) have specifically tailored a cognitive remediation therapy (CRT) for treating Anorexia Nervosa (AN). It is an intensive manualised training cognitive therapy which addresses the difficulties in flexibility and holistic processing that have been incriminated in AN. CRT has been found to improve AN's neuropsychological functioning and short term outcome. To our knowledge, no French speaking country has tested its effectiveness. Moreover, the question whether it is efficient for both anorexic restrictive and anorexic binge-purging patients remains unanswered.

The aim of the present study is to determine if CRT in AN adolescents and young adults has a favourable impact on cognitive functioning and clinical status. We will also explore whether the impact of CRT is similar in both anorexic restrictive and binge-purging subtypes. There will also be an Historical Control Group of patients, sixty, who received traditional medical interventions in a specialized inpatient unit for eating disorders (i.e., EVHAN study)."

Study Overview

Detailed Description

"Several studies have documented that patients with Anorexia Nervosa (AN) display a trait of cognitive inflexibility (e;g., poor set-shifting performances on the Trail Making Task B), i.e. an inability to move flexibly back and forth between tasks, operations, or mental sets which allows for the adaptation of behaviour in response to changing demands within the environment. This cognitive inflexibility can be observed both during the acute phase of the illness and after weight restoration, and has been found to predict negative treatment outcomes. 'Weak central coherence' is another skill which is particularly problematic in AN. It refers to a cognitive style in which information remains fragmented as opposed to integrated, with processing occurring at the level of 'detail' as opposed to 'whole'. AN patients exhibit this detail focussed information-processing style (e.g., as measured by the Embedded Figures Test). To treat these difficulties, clinicians from the Institute of Psychiatry (London, UK) have specifically tailored a treatment for AN. Cognitive remediation therapy (CRT) is an intensive training cognitive therapy that encourages people to reflect on and try to modify the way they think, with a particular focus on improving cognitive flexibility. It is a manualised therapist-led intervention consisting of multiple versions of a variety of tasks and mental exercises that address the difficulties in flexibility and holistic processing. CRT is a 10-sessions long program that has been found to improve AN's neuropsychological functioning and short term outcome. To our knowledge, no French speaking country has tested its effectiveness. Moreover, the question whether it is efficient for both anorexic restrictive and anorexic binge-purging patients remains unanswered.

To address these issues, we designed a multicenter randomized clinical trial on the effectiveness of CRT in AN adolescents and young adults.

Main hypothesis: AN patients treated with CRT present a better clinical status than those treated by a control therapy.

Recruitment and Procedure: 120 female adolescents or young adults [15-40 years old] AN (60 Anorexic Restrictive; 60 Anorexic Binge-Purging) will be recruited among the patients of specialized ED care units of three hospitals: PAUL BROUSSE, INSTITUT MUTUALISTE MONTSOURIS, COCHIN-MAISON DE SOLENN. In each group of AN subtype, the patients will be randomly allocated to one of the two treatment arms: CRT or Sham Therapy (ST). Each therapy is manualised and includes 10 sessions over a period of 5 weeks (2 sessions/week). All the patients will be assessed just prior the beginning and after the end of the CRT/ST, at 6 months and 1 year of follow-up."

Study Type

Interventional

Enrollment (Actual)

120

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Paris, France, 75014
        • Institut Mutualiste Monsouris
      • Paris, France, 75013
        • Clinique Villa Montsouris
      • Paris, France, 75014
        • Maison de Solenn
      • Villejuif, France, 94804
        • Assistance Publique - Hôpitaux de Paris, Hôpital Paul Brousse

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 40 years (ADULT, CHILD)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • female;
  • 15-40 years old;
  • hospitalised for a diagnosis of Anorexia Nervosa (DSM-IV Revised criteria) in one of the three departments participating in this research ;
  • fluent in French;
  • who provide their informed consent (or as far as possible their parents for those under 18).

Exclusion Criteria:

  • previous history of neurological disorders;
  • actual substance use disorder;
  • schizophrenia;
  • presenting a related somatic illness (diabetes, Crohn's disease, metabolic illness) or a life-threatening condition.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
ACTIVE_COMPARATOR: Cognitive Remediation Therapy (CRT)
Active : CRT
Cognitive remediation therapy (CRT) is an intensive training cognitive therapy that encourages people to reflect on and try to modify the way they think, with a particular focus on improving cognitive flexibility. It is a manualised therapist-led intervention consisting of multiple versions of a variety of tasks and mental exercises that address the difficulties in flexibility and holistic processing. CRT is an individual 10-sessions long program (2 sessions per week).
Other Names:
  • CRT
SHAM_COMPARATOR: Sham Therapy (ST)
Sham : ST
The Sham therapy (ST) has been designed to match the CRT format: an individual manualised therapist-led 10-sessions long program (2 sessions per week). ST sessions have been designed so as to avoid set-shifting and central coherence training. Rather, ST is a manualised sham intervention consisting of multiple exercises on 3 domains: soft physical activity, emotional expression recognition and interpersonal functioning.
Other Names:
  • ST

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Neuropsychological functioning:Wisconsin Sorting Card Test (WSCT)
Time Frame: 1 week post-therapy
The WSCT are two neuropsychological tests that have been consistently used to highlight poor set-shifting skills in Anorexia nervosa.
1 week post-therapy
Clinical status Evaluation:Morgan and Russell Global Outcome Assessment Scale (GOAS);
Time Frame: up to 1 year of follow-up
The Global Outcome Assessment Schedule (GOAS; Morgan & Hayward, 1998) is a standard measure of outcome in eating disorders; it includes 14 subscales evaluating five dimensions: (A) Food Intake and body weight ; (B) Menstrual status; (C) Mental state ; (D) Psychosexual state ; (E) Socioeconomic status and social functioning.
up to 1 year of follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Central coherence
Time Frame: 1 week post-therapy
Central coherence: Rey figure;
1 week post-therapy
Nutritional status
Time Frame: 1 week post-therapy
body mass index
1 week post-therapy
Nutritional status
Time Frame: 6 months of follow-up
body mass index
6 months of follow-up
Nutritional status
Time Frame: 1 year of follow-up
body mass index
1 year of follow-up
Self-reported eating disorders symptoms
Time Frame: 1 week post-therapy
Eating Disorder Examination Questionnaire and Body Shape Questionnaire
1 week post-therapy
Self-reported eating disorders symptoms
Time Frame: 1 year of follow-up
Eating Disorder Examination Questionnaire and Body Shape Questionnaire
1 year of follow-up
Self-reported Cognitive style;
Time Frame: 1 week post-therapy
Detail and Flexibility Questionnaire
1 week post-therapy
Self-reported Cognitive style;
Time Frame: 1 year of follow-up
Detail and Flexibility Questionnaire
1 year of follow-up
Self-reported treatment satisfaction
Time Frame: 1 week post-therapy
Helping Alliance Questionnaire and Patient Satisfaction Questionnaire
1 week post-therapy
Self-reported motivation to change
Time Frame: 1 week post-therapy
the Maudsley motivation to change questionnaire
1 week post-therapy
Self-reported motivation to change
Time Frame: 6 months of follow-up
the Maudsley motivation to change questionnaire
6 months of follow-up
Self-reported motivation to change
Time Frame: 1 year of follow-up
the Maudsley motivation to change questionnaire
1 year of follow-up
Self-reported self-esteem
Time Frame: 1 week post-therapy
Rosenberg self-esteem Questionnaire
1 week post-therapy
Self-reported self-esteem
Time Frame: 1 year of follow-up
Rosenberg self-esteem Questionnaire
1 year of follow-up
Flexibility evolution : Trail Making Test (TMT)
Time Frame: 1 week post-therapy
Neuropsychological functioning
1 week post-therapy

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Sylvie BERTHOZ, PhD, Institut National de la Santé Et de la Recherche Médicale, France
  • Principal Investigator: Damien RINGUENET, MD, Assistance Publique - Hôpitaux de Paris

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2012

Primary Completion (ACTUAL)

June 1, 2016

Study Completion (ACTUAL)

January 1, 2017

Study Registration Dates

First Submitted

January 17, 2013

First Submitted That Met QC Criteria

January 17, 2013

First Posted (ESTIMATE)

January 21, 2013

Study Record Updates

Last Update Posted (ESTIMATE)

January 16, 2017

Last Update Submitted That Met QC Criteria

January 13, 2017

Last Verified

January 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • RCB-2011-A01280-41
  • P091123 (OTHER: AP-HP)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Young Adult

Clinical Trials on Cognitive Remediation Therapy

3
Subscribe