Effects of a Yoga-Based Course in Preventing Disordered Eating in Female Collegiate Athletes

September 27, 2022 updated by: Catherine Cook-Cottone, University at Buffalo

Effects of a Yoga-Based Course in Preventing Disordered Eating in Female Collegiate Athletes: A Controlled Study

The purpose of the study is to evaluate effects of a 7-week undergraduate course, incorporating Eat Breathe Thrive program curriculum, offered to female student-athletes in order to increase positive body image, emotional regulation, interoceptive awareness, self-care skills, and intuitive eating. The undergraduate course is structured around the Eat Breathe Thrive program curriculum, which aims to: a) teach somatic practices that increase interoceptive awareness, b) provide healthy tools for emotional regulation, c) allow for the creation of community-based networks of support, and (d) foster a sense of meaning and purpose through service activities. In a non-randomized controlled trial, the investigators plan to examine whether this preventative undergraduate course is found effective in a female student-athlete population in preventing and decreasing eating disorder risk. The investigators also plan to examine whether the program is found effective in increasing protective factors, such as self-care behaviors, interoceptive awareness, intuitive eating, and emotional regulation skills.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

To the investigators' knowledge, there are no studies that incorporate yoga into eating disorder prevention intervention in a student-athlete population, indicating a gap in literature that the proposed study aims to address. In this study, a 7-week undergraduate course offered to female student-athletes, which incorporates Eat Breathe Thrive program curriculum, will be examined to evaluate preventative effects. The Eat Breathe Thrive program was selected by the course instructors to provide female student-athletes with mental health support, utilizing an interactive multisession format with a positive psychology orientation. Eat Breathe Thrive's curriculum focuses on the reduction of eating disorder risk by lesson plans centered around positive engagement with others and developing a strong relationship with self. This framework is based on the idea that individuals are able to sustain proper health, relationships, and overall well-being using the positive embodiment tools and psychoeducational information learned. The study aims to contribute to the eating disorder literature targeting female student-athletes by examining the effects of a prevention program delivered as part of an undergraduate course.

It is hypothesized that:

  • Prevention course participants will show a decrease in disordered eating behaviors when compared to controls.
  • Prevention course participants will show an increase in self-care behaviors compared to controls.
  • Prevention course participants will show an increase in interoceptive awareness, intuitive eating, and emotional regulation when compared to controls.
  • Prevention course participants will show a decrease in difficulties with emotional regulation and an increase in tolerance to distress when compared to controls.
  • Prevention course participants will show better maintenance of wellbeing as well as better maintenance in decreased symptomatology as compared to compared to controls.

The study will employ self-report surveys to examine the preventative effects of participation in a 7-week course utilizing a longitudinal non-randomized control design with Division I female student-athletes in western New York. Participants will be current female student-athletes recruited within the university's athletic department. Experimental group participants will be recruited from their enrollment in the prevention course offered that incorporates the Eat Breathe Thrive curriculum. Since the prevention course has a capacity of 30 students per semester, data will be collected for four 7-week semesters to account for total sample size. The study will be recruiting from a total of 120 female student-athletes in the experimental group. Female student-athletes not enrolled in the prevention course will be recruited for control. Each semester, course enrollment numbers will be matched by recruiting research participants from the rest of the female student-athlete population at the university (those who are not enrolled in the course). Female student-athletes in the experimental and control groups will complete all study measures at the same time points throughout the study. This study is based on the need to provide female student-athletes with greater access to effective tools and strategies that support their well-being as well as to protect this high-risk population against the development of an eating disorder.

Study Type

Observational

Enrollment (Actual)

108

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New York
      • Buffalo, New York, United States, 14260
        • Center for Excellence in Academic and Athletic Performance

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 24 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Participants are from the undergraduate student-athlete population at the university who are currently a member of one of the Division I sports teams. Specifically, female undergraduate student-athletes, ranging from ages 18-24.

Description

Inclusion Criteria:

  • Participant is a female undergraduate student-athletes at the university

Exclusion Criteria:

  • There are no exclusion criteria not already covered within the criteria for inclusion stated

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Prevention Course Group
The Prevention Course Group is composed of female student-athletes enrolled in the 7-week prevention course. The course occurs once a week (1 hour, 40 minute sessions) for a total of 7-weeks during the academic semester. Approximately 1 hour of each class session is lecture based, leaving 40 minutes for yoga practice administered by a certified yoga instructor. The course instructor is certified in Eat Breathe Thrive Program delivery. The course teaching assistant is certified in yoga instruction.
The undergraduate prevention course is structured around Eat Breathe Thrive Program curriculum. The course aims to teach somatic practices, provide healthy tools for emotional regulation, allow for the creation of community-based networks of support, foster a sense of meaning and purpose through service activities, and practice these learned skills through yoga.
Other Names:
  • Eat Breathe Thrive Program
Control Group
The Control Group is composed of female student-athletes not enrolled in the 7-week prevention course. Female student-athletes in this group will not be enrolled in the course during the period of data collection, nor will they have previously completed the course.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Disordered Eating Behaviors
Time Frame: Change from Baseline in Eating Disorder Examination Questionnaire at 7 weeks
Change in Eating Disorder Examination Questionnaire
Change from Baseline in Eating Disorder Examination Questionnaire at 7 weeks
Self-Care Behaviors
Time Frame: Change from Baseline in Mindful Self-Care Scale-Short at 7 weeks
Change in Mindful Self-Care Scale-Short
Change from Baseline in Mindful Self-Care Scale-Short at 7 weeks
Interoceptive Awareness
Time Frame: Change from Baseline in Multidimensional Assessment of Interoceptive Awareness at 7 weeks
Change in Multidimensional Assessment of Interoceptive Awareness
Change from Baseline in Multidimensional Assessment of Interoceptive Awareness at 7 weeks
Emotional Regulation
Time Frame: Change from Baseline in Difficulties in Emotion Regulation Scale at 7 weeks
Change in Difficulties in Emotion Regulation Scale
Change from Baseline in Difficulties in Emotion Regulation Scale at 7 weeks
Distress Tolerance
Time Frame: Change from Baseline in Distress Tolerance Scale and State-Trait Anxiety Inventory for Adults at 7 weeks
Change in Distress Tolerance Scale and State-Trait Anxiety Inventory for Adults
Change from Baseline in Distress Tolerance Scale and State-Trait Anxiety Inventory for Adults at 7 weeks
Intuitive Eating
Time Frame: Change from Baseline in Intuitive Eating Scale in 7 weeks
Change in Intuitive Eating Scale
Change from Baseline in Intuitive Eating Scale in 7 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Disordered Eating Behaviors
Time Frame: Change from Baseline in Eating Disorder Examination Questionnaire at 19 weeks
Change in Eating Disorder Examination Questionnaire
Change from Baseline in Eating Disorder Examination Questionnaire at 19 weeks
Self-Care Behaviors
Time Frame: Change from Baseline in Mindful Self-Care Scale-Short at 19 weeks
Change in Mindful Self-Care Scale-Short
Change from Baseline in Mindful Self-Care Scale-Short at 19 weeks
Emotional Regulation
Time Frame: Change from Baseline in Difficulties in Emotion Regulation Scale at 19 weeks
Change in Difficulties in Emotion Regulation Scale
Change from Baseline in Difficulties in Emotion Regulation Scale at 19 weeks
Distress Tolerance
Time Frame: Change from Baseline in Distress Tolerance Scale and State-Trait Anxiety Inventory for Adults at 19 weeks
Change in Distress Tolerance Scale and State-Trait Anxiety Inventory for Adults
Change from Baseline in Distress Tolerance Scale and State-Trait Anxiety Inventory for Adults at 19 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Catherine Cook-Cottone, PhD, Counseling, School, and Educational Psychology

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 24, 2018

Primary Completion (Actual)

June 30, 2019

Study Completion (Actual)

June 30, 2019

Study Registration Dates

First Submitted

November 15, 2017

First Submitted That Met QC Criteria

November 15, 2017

First Posted (Actual)

November 20, 2017

Study Record Updates

Last Update Posted (Actual)

September 29, 2022

Last Update Submitted That Met QC Criteria

September 27, 2022

Last Verified

September 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • EBTSA01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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