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Web-based guided self-help cognitive behavioral therapy-enhanced versus treatment as usual for binge-eating disorder: a randomized controlled trial protocol.
van Beers, Ella; Melisse, Bernou; de Jonge, Margo; Peen, Jaap; van den Berg, Elske; de Beurs, Edwin.
Affiliation
  • van Beers E; Novarum Center for Eating Disorders & Obesity, Amstelveen, Netherlands.
  • Melisse B; Novarum Center for Eating Disorders & Obesity, Amstelveen, Netherlands.
  • de Jonge M; Utrecht University, Department of Clinical Psychology, Utrecht, Netherlands.
  • Peen J; Novarum Center for Eating Disorders & Obesity, Amstelveen, Netherlands.
  • van den Berg E; Department of Research, Arkin Mental Health Institute, Amsterdam, Netherlands.
  • de Beurs E; Novarum Center for Eating Disorders & Obesity, Amstelveen, Netherlands.
Front Psychiatry ; 15: 1332360, 2024.
Article in En | MEDLINE | ID: mdl-38435976
ABSTRACT
Binge-eating disorder (BED) is a psychiatric disorder characterized by recurrent episodes of eating a large amount of food in a discrete period of time while experiencing a loss of control. Cognitive behavioral therapy-enhanced (CBT-E) is a recommended treatment for binge-eating disorder and is typically offered through 20 sessions. Although binge-eating disorder is highly responsive to CBT-E, the cost of treating these patients is high. Therefore, it is crucial to evaluate the efficacy of low-intensity and low-cost treatments for binge-eating disorder that can be offered as a first line of treatment and be widely disseminated. The proposed noninferiority randomized controlled trial aims to determine the efficacy of web-based guided self-help CBT-E compared to treatment-as-usual CBT-E. Guided self-help will be based on a self-help program to stop binge eating, will be shorter in duration and lower intensity, and will require fewer therapist hours. Patients with binge-eating disorder (N = 180) will be randomly assigned to receive guided self-help or treatment-as-usual. Assessments will take place at baseline, mid-treatment, at the end of treatment, and at 20- and 40-weeks post-treatment. Treatment efficacy will be measured by examining the reduction in binge-eating days in the previous 28 days between baseline and the end of treatment between groups, with a noninferiority margin (Δ) of 1 binge-eating day. Secondary outcomes will include full remission, body shape dissatisfaction, therapeutic alliance, clinical impairment, health-related quality of life, attrition, and an economic evaluation to assess cost-effectiveness and cost-utility. The moderators examined will be baseline scores, demographic variables, and body mass index. It is expected that guided self-help is noninferior in efficacy compared to treatment-as-usual. The proposed study will be the first to directly compare the efficacy and economically evaluate a low-intensity and low-cost binge-eating disorder treatment compared to treatment-as-usual. If guided self-help is noninferior to treatment-as-usual in efficacy, it can be widely disseminated and used as a first line of treatment for patients with binge-eating disorder. The Dutch trial register number is R21.016. The study has been approved by the Medical Research Ethics Committees United on May 25th, 2021, case number NL76368.100.21.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Psychiatry Year: 2024 Document type: Article Affiliation country: Países Bajos Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Psychiatry Year: 2024 Document type: Article Affiliation country: Países Bajos Country of publication: Suiza