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Intervention Program to Improve Body Image and Self-Esteem Among Female Athletes.

This study is enrolling participants by invitation only.
Sponsor:
Information provided by (Responsible Party):
Tel Hai College
ClinicalTrials.gov Identifier:
NCT03211468
First received: May 7, 2017
Last updated: July 5, 2017
Last verified: July 2017
  Purpose
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.

Condition Intervention
Feeding and Eating Disorders Behavioral: Clinical intervention program to prevent eating disorders

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: No masking
Primary Purpose: Prevention
Official Title: Effectiveness of an Intervention Program to Improve Body Image and Self-Esteem Among Female Adolescent Aesthetic Athletes.

Resource links provided by NLM:


Further study details as provided by Tel Hai College:

Primary Outcome Measures:
  • Change in results of study questionnaire. [ Time Frame: Each participant shall be assessed for a total duration of 6 months. ]
    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.


Estimated Enrollment: 100
Actual Study Start Date: May 1, 2017
Estimated Study Completion Date: June 2018
Estimated Primary Completion Date: March 2018 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Intervention Program
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.
Behavioral: Clinical intervention program to prevent eating disorders
See previous
No Intervention: Control Group
No participation in intervention program.

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.
  Eligibility

Ages Eligible for Study:   10 Years to 16 Years   (Child)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Accepts Healthy Volunteers:   Yes
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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT03211468

Locations
Israel
Academic College of Tel Hai
Kiryat Shmona, North of Israel, Israel, 1220800
Sponsors and Collaborators
Tel Hai College
  More Information

Responsible Party: Tel Hai College
ClinicalTrials.gov Identifier: NCT03211468     History of Changes
Other Study ID Numbers: Tel Hai College
Study First Received: May 7, 2017
Last Updated: July 5, 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Feeding and Eating Disorders
Mental Disorders

ClinicalTrials.gov processed this record on July 11, 2017