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Health BehaviorNCT04077177

Decreasing Body Dissatisfaction in Male College Athletes: A Randomized Controlled Trial of the Male Athlete Body Project

A study testing Male Athlete Body Project in people with Health Behavior, run by Illinois Institute of Technology at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Body Dissatisfaction (BD) is associated with marked distress and often precipitates disordered eating symptomology (Milligan \& Pritchard, 2006). BD in male athletes is an important area to explore, as research in this field often focuses on eating disorders in female athletes (e.g., Becker et al., 2012; Varnes et… Read more about this study

Who is it for?
Ages 18 to 50 years, men onlyHealthy volunteers can take part
Conditions the study is for
Health Behavior
What is being tested?
Male Athlete Body Project
Could I receive a placebo?
No, everyone receives an active treatment
How many people
83 participants
Where
1 siteUnited States
Study dates
15 Feb 2019to 20 Mar 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 50 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Male
  • member of a university-sponsored varsity athletic team
  • over age 18
  • some endorsement of body dissatisfaction (i.e., scores greater than zero). To maximize generalizability, there are no additional inclusion criteria, consistent with recommendations from previous athlete Body Project research

Who cannot join

  • NONE

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Illinois Institute of Technology

    Chicago, Illinois, 606016

Other trials in United States

About this study

Body Dissatisfaction (BD) is associated with marked distress and often precipitates disordered eating symptomology (Milligan \& Pritchard, 2006). BD in male athletes is an important area to explore, as research in this field often focuses on eating disorders in female athletes (e.g., Becker et al., 2012; Varnes et al., 2013). The current body of literature regarding male college athletes suggests that they experience pressures associated with both societal muscular ideals and sport performance (Galli et al., 2015). While there is a clear association between drive for muscularity and BD in collegiate male athletes (Galli et al., 2015), no study to date has conducted research aimed to attenuate the effect of BD in this population. The current study seeks to investigate a BD intervention for male college athletes. Participants will be randomized to an adapted version of the standardized Female Athlete Body Project (i.e., the Male Athlete Body Project) or an assessment only control condition. All participants will complete baseline and post-treatment measures of BD, negative affect, internalization of an athletic ideal, drive for muscularity, sport confidence, eating pathology, and unhealthy weight-control behaviors. Study aims are to determine if the Male Athlete Body Project intervention group reduces BD and related factors post-treatment, and to investigate whether these differences are maintained at 1-month follow up. Results will inform mental health and sport clinicians, coaches, and other personnel involved in an athlete's care about successful strategies for decreasing BD.

Conditions
Health Behavior
Being tested
Male Athlete Body Project
Medical subject headings
Health Behavior

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Male Athlete Body ProjectBehavioural

    Participants who meet eligibility criteria and consent to the study will be randomized to one of two conditions: intervention condition (i.e., Male Athlete Body Project) or an assessment only control condition. The intervention groups will take place at IIT. Participants who accept randomization to condition will complete baseline questionnaires after randomization (immediately prior to Session 1 in the intervention condition and after being randomized to the assessment only control condition). Questionnaires will be repeated immediately post-intervention (intervention condition)/after a 3-week interval (control). All participants will be asked to complete the questionnaires again, 4 weeks after the previous round of questionnaires. The 3, 80-minute group sessions will be separated by 1 week.

Study groups in NCT04077177
Study groupRoleWhat they receive
Assessment OnlyNo interventionNot described
InterventionExperimentalNot described
Receives: Behavioral: Male Athlete Body Project

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change is being assessed with Multidimensional Body-Self Relations Questionnaire (MBSRQ) - Appearance Scale

    This measure assesses body dissatisfaction and appearance concerns over 34 items. The total score will not be interpreted; instead, subscale scores will be reported and interpreted. The subscales are: Appearance Evaluation, Appearance Orientation, Overweight Preoccupation, Self-Classified Weight, and the Body Areas Satisfaction Scale. For the Appearance Evaluation subscale, higher scores indicate a better outcome. Scores range from 7-35. For Appearance Orientation, higher scores indicate a worse outcome. Scores range from 12-60. For the Overweight Preoccupation subscale, higher scores represent a worse outcome. Scores range from 4-20. For Self-Classified Weight, higher scores represent the individual believing they are overweight. Scores range from 2-8. For the Body Areas Satisfaction Scale, higher scores indicate a better outcome. Scores range from 9-45.

    Measured: Participants will complete this at baseline, 3-week follow up, and 1-month follow-up

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Sep 2019
  2. Study start15 Feb 2019
  3. Primary completion20 Mar 2020
  4. Study completion20 Mar 2020

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
83 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04077177
Sponsor's protocol ID
IllinoisIT
Status last verified
Sep 2020
First submitted
5 Aug 2019
Last updated
28 Sep 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Perelman H, Schwartz N, Yeoward-Dodson J, Quinones IC, Murray MF, Dougherty EN, Townsel R, Arthur-Cameselle J, Haedt-Matt AA. Reducing eating disorder risk among male athletes: A randomized controlled trial investigating the male athlete body project. Int J Eat Disord. 2022 Feb;55(2):193-206. doi: 10.1002/eat.23665. Epub 2022 Jan 17.

    PubMed 35037275

Questions about this trial

What is this clinical trial studying?

A study testing Male Athlete Body Project in people with Health Behavior, run by Illinois Institute of Technology at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Sep 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change is being assessed with Multidimensional Body-Self Relations Questionnaire (MBSRQ) - Appearance Scale (time frame: Participants will complete this at baseline, 3-week follow up, and 1-month follow-up). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04077177, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Sep 2020.

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