HSP: Healthy Sport Project; Preventing Eating Disorders in Sport

Sponsor
Ostfold University College (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05583162
Collaborator
Norwegian School of Sport Sciences (Other), Oslo University Hospital (Other)
90
1
1
5.7
15.7

Study Details

Study Description

Brief Summary

The "Healthy Sport Project" is an adapted program from the Body Project by prof Eric Stice, aiming to reduce body dissatisfaction and symptoms of disordered eating and eating disorders in adolescent elite athletes. This trial aim to evaluate the effect of the program using a one-arm pilot study design in 14 years age old athletes at a Norwegian Elite Sport Junior High School.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Healthy Sport Project
N/A

Detailed Description

Eating disorders (EDs) are serious illnesses with highest incidence in adolescents. Moreover, athletes have a higher frequency of symptoms of disordered eating (DE) and EDs than non-athletes. There are many reasons to this health issue, but body appearance pressure, competing in body mass sensitive sports, and comments on body appearance are important explanations. Few programs have proved effective in preventing DE and EDs in the general population, or in athletes specifically, and none is permanent operative in sports in Norway. Body Project by prof Eric Stice have proved effective in preventing body dissatisfaction, figure idealization and new onset of EDs in female adolescents above 15 years of age, and with body dissatisfaction, from the general population. A few attempts to adapt this program to female athletes, argue for a comparative positive effect. Three important elements to further address, are: 1) programs need also to be tested in males; 2) programs need to be tested in adolescents of younger age before the typical onset of an ED; and 3) programs need to be possible to administer by non-professionals.

In this study the research group aim to adapt and test the effect of the Body Project, by the pilot study the "Healthy Sport Project", in elite junior athletes attending specialized junior sport high schools (age 14). The final goal for this project group is to create an effective preventive program for body dissatisfaction and DE/EDs in young athletes of both sexes and in mixed sports, and which may be administered by the schoolteachers.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
A cohort of athletes receive intervention in this pilot study, and changes from pre to post intervention are evaluatedA cohort of athletes receive intervention in this pilot study, and changes from pre to post intervention are evaluated
Masking:
None (Open Label)
Masking Description:
Masking is not performed in a one-arm study
Primary Purpose:
Prevention
Official Title:
Healthy Sport Project: "Recovery, Body Acceptance and Health in Young Athletes"
Actual Study Start Date :
Aug 10, 2022
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Jan 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

All pupils attending a Elite Sport Jr High School receive intervention

Behavioral: Healthy Sport Project
2 interactive information lectures (given per class of 30 pupils), and 4 interactive workshops (given to sex-homogenous groups of 10 pupils). One per week, a total of 6 weeks with intervention.
Other Names:
  • Sports Body Project
  • Outcome Measures

    Primary Outcome Measures

    1. Change in symptoms of Eating Disorder, Eating Disorder Questionnaire Short-form [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      9 Questions on eating restriction, on worries for body weight and appearance. Rated by number of days the different content has been relevant. By Fairburn and Beglin, 2008

    2. Change in Body Acceptance, Body Acceptance Scale, version 2 [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      10 Questions on body acceptance, rated by a 5 point Likert Scale (never - always). By Halliwell et al 2017.

    3. Change in symptoms of internalization of body figure ideals, SATAQ-4 [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      10 Questions from subscales of SATAQ-4 (thinness idealisation and muscularity idealization), rated by 5 point Likert Scale. By Schaefer et al 2015

    4. Experiences from participating in the project [After intervention (post, +6 weeks)]

      Focus group interview following a semistructured manual; asking for experiences with participation in the "Healthy Sport Project"

    Secondary Outcome Measures

    1. Change in experiences of Body Appearance Pressure (BAP), questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Question on experience of BAP (if it is experienced yes/no)

    2. Change in experiences of Body Appearance Pressure (BAP), questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Question on arenas for experience of BAP (in which contexts; choose between listed arenas)

    3. Change in dietary habits, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Questions on meal frequency (numbers); frequency of intake of fruit and vegetables (number of portions); frequency of intake of dairy products (number of portions); frequency of intake of fish (number of portions)

    4. Change in dietary habits, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Use of supplements (yes/no)

    5. Change in dietary habits, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Use of supplements ( what type of supplements, chose from listed alternatives)

    6. Change in nutrition knowledge, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      3 questions asking for examples of foods providing carbohydrates; proteins; fats, respectively.

    Other Outcome Measures

    1. Question on injuries, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      1 Questions asking for any incident of injury (yes/no)

    2. Question on injuries, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Where the injury was located (chose from list of anatomical locations)

    3. Demographics, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Age (years)

    4. Demographics, questions by research group [Before intervention]

      Sex (male/female)

    5. Demographics, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Sport (any given)

    6. Demographics, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Body weight (kg)

    7. Demographics, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Height (m)

    8. Demographics, questions by research group [Before intervention, After intervention (post, +6 weeks), 6 months after end of intervention]

      Number of hours in physical activity per week (hours).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    13 Years to 14 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • pupil at the recruited Sport Jr High School
    Exclusion Criteria:
    • no informed consent from parents

    • not willing to participate

    • a diagnosis of an eating disorder and being under (or waiting for) treatment

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Therese Fostervold Mathisen Fredrikstad Norway 1671

    Sponsors and Collaborators

    • Ostfold University College
    • Norwegian School of Sport Sciences
    • Oslo University Hospital

    Investigators

    • Principal Investigator: Therese F Mathisen, PhD, Østfold University College

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Therese Fostervold Mathisen, Associate Professor, Ostfold University College
    ClinicalTrials.gov Identifier:
    NCT05583162
    Other Study ID Numbers:
    • 277766
    First Posted:
    Oct 17, 2022
    Last Update Posted:
    Oct 20, 2022
    Last Verified:
    Oct 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Therese Fostervold Mathisen, Associate Professor, Ostfold University College
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 20, 2022