Skip to main content
Clinical Trials/NCT04573530
NCT04573530
Active, Not Recruiting
N/A

We Walk Plus Study: A Walking Program Using Physical Activity Monitors and Social Networking for Older Adults With Intellectual Disabilities

University of Illinois at Chicago2 sites in 1 country46 target enrollmentJune 15, 2021

Overview

Phase
N/A
Intervention
Not specified
Conditions
Intellectual Disability
Sponsor
University of Illinois at Chicago
Enrollment
46
Locations
2
Primary Endpoint
Physical activity
Status
Active, Not Recruiting
Last Updated
4 months ago

Overview

Brief Summary

Determine the feasibility and acceptability of We Walk Plus intervention to promote physical activity and improve cognition for older adults with intellectual disabilities (ID).

Detailed Description

We Walk Plus study consists of: (1) a user friendly physical activity tracker (i.e., Fitbit Charge HR ); (2) user-centered social networking (e.g., Fitbit community); and (3) the iCardia platform for monitoring daily Fitbit physical activity and wear time and sending personalized text-messages targeting physical activity and self-efficacy. The specific aims of this two-arm RCT pilot are to: 1) assess the feasibility and acceptability of the We Walk Plus intervention and 2) explore the preliminary efficacy of We Walk Plus on physical activity and well-being.

Registry
clinicaltrials.gov
Start Date
June 15, 2021
End Date
February 15, 2026
Last Updated
4 months ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kueifang Hsieh

Research Associate Professor

University of Illinois at Chicago

Eligibility 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.

Outcomes

Primary Outcomes

Physical activity

Time Frame: 12 weeks

daily steps

Secondary Outcomes

  • Self-efficacy to physical activity(12 weeks)
  • Attention & executive function(12 weeks)
  • Executive function(12 weeks)
  • Cardiovascular fitness(12 weeks)
  • Working memory(12 weeks)
  • Processing speed(12 weeks)

Study Sites (2)

Loading locations...

Similar Trials