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Body Image Intervention Program for Student Athletes' Well-Being
Phase 3
Recruiting
Led By Daniel Taylor, Ph.D
Research Sponsored by University of Arizona
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up pre-intervention, 1-2 weeks, 4 months and 12 months post intervention
Awards & highlights
Study Summary
This trial will assess if a program can help athletes improve body image, eating concerns, and overall psychological well-being. Research suggests program can improve mental health of participants.
Who is the study for?
This trial is for current student-athletes who are at least 18 years old and attending a Pac-12 University. Participants must be fluent in English. The study aims to help those with body image concerns, regardless of their gender identity.Check my eligibility
What is being tested?
The 'Bodies in Motion' (BIM) program is being tested for its ability to improve body image, reduce eating disorders, and enhance psychological well-being among student athletes from diverse backgrounds.See study design
What are the potential side effects?
Since BIM is a psychological intervention program rather than a medication, it may not have typical physical side effects but could include emotional discomfort or distress during the process.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ pre-intervention, 1-2 weeks, 4 months and 12 months post intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~pre-intervention, 1-2 weeks, 4 months and 12 months post intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change between baseline and post intervention Body Parts Satisfaction Scale-Revised (BPSS-R)
Change between baseline and post intervention Self-Compassion Scale - Short Form (SCS-SF)
Change between baseline and post intervention Sociocultural Attitudes Toward Appearance Questionnaire
+2 moreSecondary outcome measures
Eating Disorder Examination Questionnaire-Short Form (EDE-QS)
Generalized Anxiety Disorder-2 Item (GAD-2)
Patient Health Questionnaire-2 Item (PHQ-2
Trial Design
1Treatment groups
Experimental Treatment
Group I: BIM intervention participantsExperimental Treatment1 Intervention
Specifically, at each of the seven intervention sites, a minimum of 30 male and 30 female-identifying student athletes will participate in the BIM program across the 2022-2023 academic year. Thus, our intervention sample will be a minimum of 210 male and 210 female identifying intervention group athletes. The BIM program is a manualized intervention that consists of a 35-min introductory session, followed by four, 75-min sessions. Athletes participating in BIM who give consent (via electronic consent documentation) to share their de-identified data for research purposes will complete additional surveys beyond the standard MH-CDE set of baseline measures at one time-point and treatment-related measures at five time-points:
Pre-intervention/Baseline
Post-intervention (1-2 weeks after)
4-months post-intervention
12-months post-intervention
Find a Location
Who is running the clinical trial?
University of ArizonaLead Sponsor
515 Previous Clinical Trials
148,294 Total Patients Enrolled
University of North Texas Health Science CenterOTHER
39 Previous Clinical Trials
19,752 Total Patients Enrolled
Daniel Taylor, Ph.DPrincipal InvestigatorUniversity of Arizona
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am 18 or older and at a Pac-12 University.I am currently a student-athlete.
Research Study Groups:
This trial has the following groups:- Group 1: BIM intervention participants
Awards:
This trial has 2 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How many participants are currently recruited to this experiment?
"Affirmative. Clinicaltrials.gov indicates that this research project is actively seeking participants, having been first posted on September 20th 2022 and last updated on May 8th 2023. The trial necessitates 420 patients to be recruited from a single medical facility."
Answered by AI
Are the criteria for volunteer enrollment in this clinical trial age-specific?
"This clinical trial is recruiting patients aged between 18 and 25 years old."
Answered by AI
What safety measures are in place to ensure the wellbeing of participants taking this treatment?
"We have calculated the safety of this therapeutic intervention to be a 3, as it is currently in Phase 3 trials. This means there are multiple validations supporting its efficacy and numerous rounds that have proven safety."
Answered by AI
Who has the capability to participate in this research trial?
"Those looking to enter this medical trial must have a history of disordered eating, and be within the age range of 18 to 25. As such, 420 participants will eventually join in on this clinical research project."
Answered by AI
Are there any vacancies available for participation in this clinical trial?
"Affirmative. Clinicaltrials.gov data confirms that this research project, which was initially posted on September 20th 2022, is actively recruiting patients. The trial aims to enlist 420 individuals from 1 medical centre."
Answered by AI
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