- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06724796
Yoga 4 Body Image (Y4BI): Investigating the Impact of Yoga on Body Image and Eating Behaviours (Y4BI)
Yoga 4 Body Image (Y4BI): Investigating the Impact of Yoga on Body Image and Eating Behaviours in Young Women
The practice of yoga can positively impact body image, a psychological construct encompassing perceptual, emotional, cognitive, and behavioral aspects, which can be either positive or negative. Negative body image manifests as extreme dissatisfaction with one's body-a condition particularly common among young women-that places them at significant risk for developing Body Image Disorders (BIDs). In contrast, positive body image is characterized by an overall respect for one's body.
Current research on the impact of yoga on body image has several limitations, making it challenging to determine whether yoga practice truly has a positive effect on body image and to identify the mechanisms underlying this impact. To address these gaps, the present project aims to overcome the limitations of existing studies by investigating the impact of yoga on body image through quantitative methodologies and by exploring the mechanisms that drive this effect.
The project consists of two phases:
- Investigating the impact of yoga on body image (both positive and negative) and eating behaviours in a population characterized by high levels of body dissatisfaction-young women.
- Examining the psychological mechanisms underlying yoga's impact on body image, including increased interoceptive awareness, embodiment, and self-compassion, as well as a reduction in self-objectification.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Silvia Cerea, PhD
- Phone Number: ++39 049 827 6683
- Email: silvia.cerea@unipd.it
Study Locations
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-
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Padova, Italy
- Recruiting
- Department of General Psychology, University of Padova
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Contact:
- Silvia Cerea, PhD
- Phone Number: ++39 049 827 6683
- Email: silvia.cerea@unipd.it
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Females
- Age 18-35 years old
Exclusion Criteria:
- Regular yoga practice
- Pregnancy
- Medical conditions that preclude yoga practice (e.g., neurodegenerative diseases, recent injuries, rheumatic conditions)
- Full-blown body image disorder
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: Y4BI
The yoga classes will be conducted once a week, in groups, with each session lasting 1 hour.
They will be led by a qualified instructor with over 10 years of teaching experience in yoga.
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The yoga classes will follow the Iyengar method, one of the most widely practiced traditional yoga styles, aimed at promoting body alignment and precision in executing poses (asanas) through the use of props such as blankets, straps, cushions, chairs, and blocks, making the poses accessible to all individuals. The classes will be conducted once a week, in groups, with each session lasting 1 hour. They will be led by a qualified instructor with over 10 years of teaching experience in yoga. The classes will be adapted for beginners who do not practice yoga regularly. |
|
Active Comparator: ACTIVE
The total body classes will take place once a week, with each session lasting one hour.
They will be led by a kinesiology specialist in preventive and adapted physical activities.
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The total body classes will take place once a week, with each session lasting one hour.
They will be led by a kinesiology specialist in preventive and adapted physical activities.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Negative Body Image
Time Frame: 10 weeks
|
Assessed with the Questionario sul Dismorfmismo Corporo (QDC; Cerea et al., 2017), a self-report questionnaire assessing negative body image made up of 40 items.
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10 weeks
|
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Body Appreciation
Time Frame: 10 weeks
|
Assessed with the Body Appreciation Scale-2 (BAS-2; Tylka & Wood-Barcalow, 2015b, Casale et al., 2021), a self-report questionnaire assessing body appreciation made up of 10 items.
|
10 weeks
|
|
Functionality Appreciation
Time Frame: 10 weeks
|
Assessed with the Functionality Appreciation Scale (FAS; Alleva, Tylka & Van Diest, 2017, Cerea et al., 2021), a self-report questionnaire assessing functionality appreciation made up of 7 items.
|
10 weeks
|
|
Dysfunctional Eating Behaviours and Risk of Developing Eating Disorders
Time Frame: 10 weeks
|
Assessed with the Eating Disorder Risk Composite Score of the Eating Disorder Inventory-3 (EDI-3; Garner, 2004; Giannini, Pannocchia, Dalla Grave, Muratori & Viglione, 2008), a self-report questionnaire assessing the risk of developing eating disorders
|
10 weeks
|
|
Functional Eating Behaviors
Time Frame: 10 weeks
|
Assessed with the Intuitive Eating Scale-2 (IES-2; Tylka & Kroon Van Diest, 2013, Swami et al., 2021), a self-report questionnaire assessing the ability to eat intuitively.
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10 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Embodiment
Time Frame: 10 weeks
|
Assessed with the Experience of Embodiment Scale (EES; Piran, Teall, & Counsell, 2020), a self-report questionnaire investigating embodiment.
|
10 weeks
|
|
Interoceptive Awareness
Time Frame: 10 weeks
|
Assessed with the Multidimensional Assessment of Interoceptive Awareness (MAIA; Mehling et al., 2012; Calì et al., 2015), a self-report questionnaire investigating interoceptive awareness
|
10 weeks
|
|
Self-compassion
Time Frame: 10 weeks
|
Assessed with the Self-Compassion Scale (SCS, Neff, 2003; Veneziani et al. 2017), a self-report questionnaire investigating self-compassion
|
10 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Other Study ID Numbers
- 389
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
product manufactured in and exported from the U.S.
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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