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Online Cognitive Behavior Therapy Enhanced for Binge Eating Disorder

Online Cognitive Behavior Therapy Enhanced for Binge Eating Disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21268
Enrollment
180
Registered
2019-08-27
Start date
2019-08-27
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Binge eating disorder, other specified eating disorder BED

Interventions

GSH CBT-E is a 12 week program. Patients have to start reading information online, to monitor their eating behavior, and to schedule, once a week, weighing, and, twice a week, self- evaluation sessio

Sponsors

This intervention will be applied at Novarum center for eating disorders and obesity, the eating disorder department of Arkin
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: (1) a DSM- 5 BED or OFSED most similar to BED classification; (2) age at least 18; (3) a BMI between 19.5 and 40; (4) moderate proficiency in Dutch and ability to read pPart one of the Dutch translation of Overcoming Binge Eating, by Christopher Fairburn (2013) , which involves psychoeducation; (5) willingness to provide contact details, including phone number, internet access, possession of a computer or tablet, and willingness to use it for treatment and research purposes.

Exclusion criteria

Exclusion criteria: (1) acute psychosis, assessed via Structural Clinical Interview by the DSM 5 (SCID -5) (First, Williams, Karg & Spitzer, 2016); (2) acute depression, assessed via SCID -5; (3) suicidal ideation, assessed via SCID -5 or (4) self-induced vomiting as compensatory behavior, as reported at initial session or EDE-interview at baseline. Other exclusion criteria are: (5) having received eating disorder treatment during the past 6 months, (6) being pregnant (7) reported use of medication with the potential to influence eating behavior such as, Lithium, Mitrazepine and anti- psychotic stimulants.

Design outcomes

Primary

MeasureTime frame
The primary outcome measure will be difference in eating disorder pathology, operationalized as the amount of days binge eating occurred, post treatment versus the waiting list control condition.

Secondary

MeasureTime frame
As secondary outcomes, differences in other eating disorder pathology defined as restraint eating, dieting, weight concern and shape concern (C. G. Fairburn & S. J. Beglin, 2008; Cooper & Fairburn, 1987), Quality of Life and clinical impairment will be assessed.

Contacts

Public ContactBernou Melisse

Novarum, centrum voor eetstoornissen en obesitas

Bernou.Melisse@novarum.nl0205904741

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)