Evaluation of Wheelchair In-Seat Activity Tracker
NCT04168450 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34
Last updated 2022-08-10
Summary
Individuals who use wheelchairs are at an increased risk of developing pressure injuries on the parts of the body that are in constant contact with the wheelchair. The development of pressure injuries can cause reduced mobility, reduced activity and participation, greater unemployment, increased risk for future pressure injury development, and premature death. There are numerous risk factors associated with developing pressure injuries. Individuals can reduce the risk of pressure injury formation by changing positions, weight-shifting, and using special cushions, but many people still struggle with pressure injuries.
This study is designed to assess the clinical effectiveness of WiSAT (Wheelchair in-Seat Activity Tracker). WiSAT is a tool designed to help prevent the development of pressure ulcers by changing behaviors that can lead to pressure ulcers. WiSAT monitors and provides real-time feedback on weight shifts and pressure relief behaviors while sitting in a wheelchair.
Conditions
- Pressure Ulcer, Buttock
- Pressure Injury
- Pressure Ulcer
Interventions
- OTHER
-
WiSAT System, Passive Feedback
The WiSAT system is installed in the participant's wheelchair cushion and a smartphone application is installed on his/her cellphone. Participants are able to view the application as they please and they will receive no notifications from the app regarding their movement goals.
- OTHER
-
WiSAT System, Active Feedback
The WiSAT system is installed in the participant's wheelchair cushion and smartphone application is installed on his/her cellphone. Participants receive notifications from the app to help them meet their movement goals.
Sponsors & Collaborators
-
Georgia Institute of Technology
collaborator OTHER -
United States Department of Defense
collaborator FED -
University of Pittsburgh
lead OTHER
Principal Investigators
-
Patricia E Karg, MS · University of Pittsburgh
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-01-13
- Primary Completion
- 2022-06-17
- Completion
- 2022-06-17
Countries
- United States
Study Locations
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