Promoting physical activity in older adults with intellectual disabilities
We Walk Plus Study: A Walking Program Using Physical Activity Monitors and Social Networking for Older Adults With Intellectual Disabilities
This study is testing a new program that uses a walking tracker and social support to help older adults with intellectual disabilities be more active and improve their well-being.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 46 (estimated) |
| Ages | 35 Years to 60 Years |
| Sex | All |
| Sponsor | University of Illinois at Chicago Academic / other |
| Locations | 2 sites (Chicago, Illinois and 1 other locations) |
| Trial ID | NCT04573530 on ClinicalTrials.gov |
What this trial studies
The We Walk Plus intervention aims to enhance physical activity and cognitive function among older adults with intellectual disabilities. This pilot study utilizes a user-friendly physical activity tracker, social networking features, and a monitoring platform to encourage participants to engage in regular walking. The study will assess both the feasibility and acceptability of the intervention while exploring its preliminary effects on participants' physical activity levels and overall well-being.
Who should consider this trial
Good fit: Ideal candidates include men and women aged 35-60 with mild to moderate intellectual disabilities who are physically inactive and can follow instructions.
Not a fit: Patients with uncontrolled hypertension, coronary disease, or those who are already physically active may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the physical health and cognitive function of older adults with intellectual disabilities.
How similar studies have performed: Other studies have shown promise in using technology to promote physical activity among older adults, indicating that this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Men and women with mild or moderate intellectual disabilities; * ages 35-60; * able to speak, read English and willing to provide consent to enroll; * able to follow instructions and walk, physically inactive; * willing to receive SMS, wear Fitbit throughout the study; * living with family or in a community residence; * support persons are willing to assist participants to ensure the Fitbit functions properly. Exclusion Criteria: * Inability to follow instructions; * diagnosis of coronary disease or uncontrolled hypertension, smokers, physically active; * participating in a health promotion program; * having mental illness or behavior problems; * support persons unable or unwilling to assist participants with Fitbit devices, if needed.
Where this trial is running
Chicago, Illinois and 1 other locations
- University of Illinois at Chicago — Chicago, Illinois, United States (Not_yet_recruiting)
- Trinity Services Inc. — New Lenox, Illinois, United States (Recruiting)
Study contacts
- Study coordinator: Kelly Hsieh, PhD
- Email: hsieh@uic.edu
- Phone: 3124131530
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.