Bariatric Surgery and Guided Self-help for Binge Eating Disorder
NCT ID: NCT02094027
Last Updated: 2016-12-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
150 participants
INTERVENTIONAL
2011-07-31
2014-12-31
Brief Summary
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The investigators hypothesize that patients who have guided self help pre-operatively will have reduced episodes of bingeing pre-operatively compared to those having treatment as usual (bariatric surgery), which will be maintained in the post-operative period, and will be associated with improved weight loss and psychological outcomes after surgery.
Detailed Description
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Guided self help for BED (GSH) is a treatment which, like bariatric surgery, is effective in reducing the number of binge episodes in people who binge eat. It is not known whether GSH prior to surgery, in patients undergoing bariatric surgery has any additional benefit for reducing bingeing, or improving weight loss in these patients.
Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Guided Self Help
Guided Self Help intervention to reduce binge eating
Guided Self Help
A behaviourally orientated guided self help book designed to reduce binge eating prior to surgery
Treatment As Usual
No intervention for binge eating (treatment as usual in the form of bariatric surgery)
Treatment As Usual
Binge eating disordered participants receive treatment as usual in the form of bariatric surgery (i.e. no pre-operative intervention to reduce binge eating)
Interventions
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Guided Self Help
A behaviourally orientated guided self help book designed to reduce binge eating prior to surgery
Treatment As Usual
Binge eating disordered participants receive treatment as usual in the form of bariatric surgery (i.e. no pre-operative intervention to reduce binge eating)
Eligibility Criteria
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Inclusion Criteria
* Pursuing bariatric surgery
Exclusion Criteria
* If the patient is taking any medication which makes them unsuitable
* If the patient is pregnant or breast feeding
* If the patient has donated blood in the last three months
* If the patient has a history of alcoholism or substance dependency within the last 5 years
* If the patient has a history of major haematological, renal, gastrointestinal, hepatic, respiratory, cardiovascular or psychiatric disease or other illness or use of any medications, including over the counter products, which, in the opinion of the investigators would either interfere with the study or potentially cause harm to the volunteer
* If the patient has any medical or psychological condition or social circumstances which would interfere with their ability to participate reliably in the trial
* If the patient is without access to a telephone
* If the patient is currently receiving or intends to receive treatment with an investigational drug within the next 2 months If the patient is currently receiving or intends to receive treatment for binge eating
* If the patient currently suffers with severe depression, as indicated by a Beck Depression Inventory Score greater than 28
18 Years
65 Years
ALL
Yes
Sponsors
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National Institute for Health Research, United Kingdom
OTHER_GOV
Imperial College London
OTHER
Responsible Party
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Principal Investigators
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Samantha Scholtz, MRCPsych
Role: PRINCIPAL_INVESTIGATOR
Imperial College London
Locations
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Obesity, Endocrine and Medical Clinics at Imperial College Healthcare NHS Trust
London, , United Kingdom
Countries
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Other Identifiers
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10/H0707/67
Identifier Type: -
Identifier Source: org_study_id