- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03262350
The Effects of Yoga on Body Image in College Women
Can Yoga Reduce Body Image Concerns in Females, Thereby Reducing Risk of Obesity and Eating Disorders?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
A randomized controlled design will be used to study the effects of a regular yoga practice on body image in young adult women. Fifty female freshman, sophomores, and juniors between the ages of 18 and 26 years will be recruited from the University of Delaware student population, specifically targeting those new to yoga. Age, academic standing, availability and prior yoga experience will be evaluated.
Consented individuals will be randomized to one of two conditions: (1) yoga (offered 3 times per week) for 10 weeks; or (2) a control group. Baseline assessments, midpoint assessments, and end-of-study assessments will be conducted on all participants. Participants will be compensated for their attendance at assessment visits.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Delaware
-
Newark, Delaware, United States, 19711
- University of Delaware
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Freshman, sophomore, or junior at the University of Delaware
- Available Spring 2017 on Mondays, Wednesdays, and Fridays from 1:25-2:15pm
- Physically able to participate in yoga
Exclusion Criteria:
- Females who are seniors at the University of Delaware (This is because participants in the control condition will be given a pass to participate in group fitness at the end of the study, and would not be able to use this incentive if they are seniors)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Yoga Group
Participants are required to attend three assessment visits.
During these assessments, participants will complete a questionnaire that will ask about their eating patterns, body image, sleep habits, and loneliness and have their height and weight measured.
Participants are also required to attend 50-minute yoga classes on Mondays, Wednesdays, and Fridays from 1:25-2:15pm for 10 weeks.
The overall time commitment for Yoga Group participants is 3 hours of assessments and 50-minute yoga classes 3X week for 10 weeks.
|
The yoga classes will be adapted to all levels of experience, mobility, and body size.
Specific breathing techniques and body positive language will be incorporated into a body-positive yoga training done by Ms. Lisa Diers, RDN, E-RYT, YACEP.
Less focus will be placed on precision of the poses, instead focus will be on body feelings, except where physically dangerous.
Thus, the overall focus will be on listening to one's own body.
List of messages will be carefully designed to be related to eating and weight, but to not be directly discussed.
Ms. Diers will travel to Delaware to lead the intervention training for yoga instructors prior to the study taking place.
|
No Intervention: Control Group
Participants will be required to attend three assessment visits.
During these assessments, participants will complete a questionnaire that will ask about their eating patterns, health habits, body image, sleep habits and loneliness and have their height and weight measured.
The overall time commitment for Control Group participants is 3 hours of assessments total.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body Image
Time Frame: 10 weeks
|
assessed using Body Image Quality of Life Inventory
|
10 weeks
|
body image
Time Frame: 10 weeks
|
assessed using Mind Body Self Relations Questionnaire
|
10 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change in Body Mass Index
Time Frame: 10 weeks
|
weight and height will be combined to report BMI in kg/m^2
|
10 weeks
|
disordered eating attitudes/behaviors
Time Frame: 10 weeks
|
assessed using the Eating Attitudes Test-26
|
10 weeks
|
disordered eating attitudes/behaviors
Time Frame: 10 weeks
|
assessed using the Binge Eating Scale
|
10 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- REF AWARD# 0001271422
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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