Intervention Program to Improve Body Image and Self-Esteem Among Female Athletes.
Primary Purpose
Feeding and Eating Disorders
Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Clinical intervention program to prevent eating disorders
Sponsored by
About this trial
This is an interventional prevention trial for Feeding and Eating Disorders
Eligibility Criteria
Inclusion Criteria:
- Female
- Age 10-16
- Athletes in aesthetic sports: figure skaters, dancers and gymnasts.
Exclusion Criteria:
- Males
- Females under age 10 or over 16
- Athletes from non-aesthetic sports
- Non-athletes.
Sites / Locations
- Academic College of Tel Hai
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention Program
Control Group
Arm Description
Clinical intervention designed to prevent eating disorders and promote healthy eating habits and body image among female adolescent athletes. The intervention program will include 10 45-min interactive sessions led by the researcher. Each session will include a brief theoretical background, experiential activities (artistic or cognitive / emotional) and group discussions.
No participation in intervention program.
Outcomes
Primary Outcome Measures
Change in results of study questionnaire.
Questionnaire shall be answered by study participants by hand or using Qualtrics online software. 3 points of assessment for each participant: baseline, post-intervention, and 3 months follow-up.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03211468
Brief Title
Intervention Program to Improve Body Image and Self-Esteem Among Female Athletes.
Official Title
Effectiveness of an Intervention Program to Improve Body Image and Self-Esteem Among Female Adolescent Aesthetic Athletes.
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
May 1, 2017 (Actual)
Primary Completion Date
April 1, 2018 (Actual)
Study Completion Date
June 1, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tel Hai College
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A controlled, randomized clinical intervention study which includes the development and activation of an intervention program designed to prevent eating disorders among adolescent female aesthetic athletes. Our hypothesis is that the intervention program will yield improvement in the participants' eating behaviors, drive for thinness, and body image as compared with the age matched control group. Results will be measured using the study questionnaire, to be filled out by the participants before, after, and three months after the completion of the program. The Questionnaire will include validated questionnaires with good psychometric qualities.
Detailed Description
Eating disorders can cause a decrease in athletic performance and affect the overall health of athletes. Athletes are exposed to an increased risk of developing pathological eating behaviors and dissatisfaction with their bodies. A number of studies have found higher rates of eating pathologies in aesthetic sports such as dance, ice skating, and gymnastics. Other studies have found that intervention programs designed to prevent eating disorders in athletes have yielded promising results. The current study will examine the effects of a controlled clinical intervention program designed to prevent eating disorders and improve the body image of female adolescent figure skaters and dancers. The program will consist of ten 45-minute interactive sessions led by the researcher. Each session will include a brief theoretical background, experiential activities (artistic or cognitive / emotional) and group discussions. The control group shall include age matched athletes who will not participate in the intervention program. The impact of the intervention shall be assessed with a nonrandomized, controlled experimental group design. To assess the impact and outcome of the intervention, all participants in the research and control groups will be asked to complete the study questionnaire at pre, post, and 3-month (after post) follow-up assessments. Process evaluation, which assesses program dissemination, attendance and relapse rates, as well as assessment of participants' satisfaction, will be performed at the end of the program. The study questionnaire includes: Personal and Demographic Information, EDI-2 (Eating Disorders Inventory), Body Esteem Scale-Mendelson, SATAQ-4 (Sociocultural Attitudes Towards Appearance Questionnaire-4), EDE-Q 8 (Eating Disorder Examination Questionnaire- 8), BAS (Body Appreciation Scale). All questionnaires have good psychometric properties. The study hypothesis is that the intervention program will result in improvement in the intervention group in terms of: disturbed eating behaviors, pursuit of thinness, body-dissatisfaction and external influences on body image compared with an age-matched control group that did not participate in the program.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Feeding and Eating Disorders
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
95 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention Program
Arm Type
Experimental
Arm Description
Clinical intervention designed to prevent eating disorders and promote healthy eating habits and body image among female adolescent athletes. The intervention program will include 10 45-min interactive sessions led by the researcher. Each session will include a brief theoretical background, experiential activities (artistic or cognitive / emotional) and group discussions.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
No participation in intervention program.
Intervention Type
Behavioral
Intervention Name(s)
Clinical intervention program to prevent eating disorders
Intervention Description
See previous
Primary Outcome Measure Information:
Title
Change in results of study questionnaire.
Description
Questionnaire shall be answered by study participants by hand or using Qualtrics online software. 3 points of assessment for each participant: baseline, post-intervention, and 3 months follow-up.
Time Frame
Each participant shall be assessed for a total duration of 6 months.
10. Eligibility
Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Female
Age 10-16
Athletes in aesthetic sports: figure skaters, dancers and gymnasts.
Exclusion Criteria:
Males
Females under age 10 or over 16
Athletes from non-aesthetic sports
Non-athletes.
Facility Information:
Facility Name
Academic College of Tel Hai
City
Kiryat Shmona
State/Province
North Of Israel
ZIP/Postal Code
1220800
Country
Israel
12. IPD Sharing Statement
Plan to Share IPD
No
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Intervention Program to Improve Body Image and Self-Esteem Among Female Athletes.
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