Reduction of Emotional Eating After a Behavior Change Program in Obesity
NCT ID: NCT01997697
Last Updated: 2021-12-08
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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COMPLETED
NA
138 participants
INTERVENTIONAL
2013-11-22
2017-11-12
Brief Summary
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Detailed Description
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* identify the barriers related to physical activity
* increase informations related to physical activity and nutrition
* informations about the risk related to inactivity and diet
* ask to the individual to list and barriers related to barriers as thhe interest to modify the behavior.
* List persons who may act as social support
* set behavior change goals
* Increase self-confidence and self-efficacy about changing behavior
* Relaxation at home
* Use reinforcement management
* methods of time management
* counter-conditioning
* identify factors related to the relapse Time management Participants will be evaluated after the first 6 months. Then, they will be followed during 24 months. Statistical analysis Sample size The sample was calculated using a previous study. To obtain a difference of 0.51 in emotional eating with a standard deviation of 1.63 with an alpha risk of 5% and a power of 90%, the number of subject is 110 subject. Expected a drop-out of 20%, 138 subjects will be included. Predictive factors
1. Identification of predictive factors Student T test to select the predictive factors
2. Predictive factors Multiple linear regression
3. Mechanisms analysis of mediation with the Baron and Kenny method
Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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Patients with obesity
behavior change program among patients with obesity
behavior change program
behavior change program among patients with obesity
Interventions
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behavior change program
behavior change program among patients with obesity
Eligibility Criteria
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Inclusion Criteria
* Age 18 to 65
* participation to the therapeutic training
* Patient with non physical activity
Exclusion Criteria
* patient taking neuroleptic or psychiatric
* pregnancy
18 Years
70 Years
ALL
No
Sponsors
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University Hospital, Montpellier
OTHER
Responsible Party
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Locations
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University Hospital of Montpellier-Hopital La colombière
Montpellier, , France
Countries
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Other Identifiers
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9110
Identifier Type: -
Identifier Source: org_study_id