Optimizing Weight Loss Outcomes Through Body Image Enhancement
NCT ID: NCT05090293
Last Updated: 2022-11-03
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
58 participants
INTERVENTIONAL
2021-09-13
2022-05-08
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Lifestyle Intervention (LI)
Participants will receive a standard, 12-week, group-delivered cognitive behavioral lifestyle intervention for weight loss.
Lifestyle Intervention (LI)
A multidisciplinary, group-delivered, multidisciplinary weight loss program addressing various lifestyle factors impacting weight loss.
Lifestyle Intervention with Body Image Treatment (LIBI)
Participants will receive a standard, 12-week, group-delivered cognitive behavioral lifestyle intervention for weight loss supplemented with a novel body image intervention designed to address body image issues in the context of weight loss.
Experimental: Lifestyle Intervention with Body Image Treatment (LIBI)
A body image protocol designed to improve outcomes in a group-delivered multidisciplinary weight loss program by addressing body acceptance within a context of positive behavior change and utilizing existing body discomfort and re-purposing it as an agent of motivation.
Interventions
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Experimental: Lifestyle Intervention with Body Image Treatment (LIBI)
A body image protocol designed to improve outcomes in a group-delivered multidisciplinary weight loss program by addressing body acceptance within a context of positive behavior change and utilizing existing body discomfort and re-purposing it as an agent of motivation.
Lifestyle Intervention (LI)
A multidisciplinary, group-delivered, multidisciplinary weight loss program addressing various lifestyle factors impacting weight loss.
Eligibility Criteria
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Inclusion Criteria
* Sex: Female
* BMI of 25 kg/m2 or greater
Exclusion Criteria
* Participants who are pregnant or planning to become pregnant over the next 4 months
* Participants who are breastfeeding or planning to breastfeed over the next 4 months
* Participants who have received a diagnosis of diabetes (type I or II)
* Participants who been told NOT to lose weight or exercise for any reason by a healthcare provider
* Participants who currently have psychiatric illnesses (e.g., Psychosis, schizophrenia, bipolar disorder or severe depression/anxiety)
* Participants who currently have persistent suicidal thoughts or have attempted suicide in the last year
* Participants with a history of diagnosed eating disorders such as bulimia nervosa or anorexia nervosa.
18 Years
FEMALE
Yes
Sponsors
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Texas Tech University
OTHER
Responsible Party
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Martin Binks
Associate Professor
Principal Investigators
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Martin Binks, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Texas Tech University- Department of Nutritional Sciences
Locations
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Texas Tech University - Department of Nutritional Sciences
Lubbock, Texas, United States
Nutrition & Metabolic Health Initiative
Lubbock, Texas, United States
Countries
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Other Identifiers
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TTUIRB2021-470
Identifier Type: -
Identifier Source: org_study_id
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