About this trial
The purpose of this study is to see if a combination of an educational curriculum and health coaching embedded within Special Olympics improves health outcomes and healthcare access compared to regular Special Olympics sport and health programming for adults with intellectual and/or developmental disabilities.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Currently participating in Special Olympics programming at a state agency in the study
Has a medical or educational diagnosis of intellectual and/or developmental disabilities
Between the ages of 21-65
Has at least weekly contact with a family member or care partner who is willing and able to participate
Disqualifiers
Inability to complete an accessible informed assent or consent process
Fluctuating capacity to consent
Trial design
Parallel
Treatments tested in this trial
Comprehensive Community Health
BehavioralParticipants will receive group health coaching, psychoeducation, and group health education.
Regular Special Olympics programming
Other interventionStandard practices for those participating in Special Olympics
Treatment groups
Trial outcomes
Primary outcomes
Change in Goal Attainment Scaling (GAS)
GAS is measured using three participant-identified goals, each assigned a priority weight from 1 to 3 (3=most important goal to participant). At each assessment, each goal is assigned a score from -2 to +2, with 0 representing expected level of attainment and 2 indicating much more than expected level of attainment; goals are assigned a score of -2 at baseline. GAS score levels across all three participant goals are converted into a standardized single GAS T-score for each participant. The range of possible T-scores is 23.56 (all three goals with GAS score of -2) to 76.44 (all three goals with GAS score of +2).
Secondary outcomes
Change in number of doctor visits
Participants will self-report how many times they visited their adult or family-care practitioner over the course of the study
Change in number of routine health check-ups
Participants will self-report whether they received routine care throughout the study
Change in number of participants with intellectual and/or developmental disabilities that follow-up with their primary physician
Participants will self-report whether they followed-up with their primary physician using HEALTH 4 ME tools to inform them of risk or concern about their health.
Change in quality of life - "Healthy Days Measure"
The CDC HRQOL-14 (Healthy Days Measures) scoring involves creating an Unhealthy Days Score by summing days with poor physical and mental health (max 30), and a Healthy Days Score (30 minus unhealthy days); individual items (general health, symptoms like pain, depression, energy) are often scored separately (0-30 for days, 1-5 for general health), with higher scores generally indicating worse health, except for energy/lack of fatigue, where higher is better. There isn't a single, complex summary score, but rather metrics for different aspects of quality of life, reported as means or percentages.
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Wisconsin, Madison
Lead sponsor
Patient-Centered Outcomes Research Institute
Collaborator
This trial is not recruiting at the moment. You can still explore other options: