Clinical Trials Directory

Trials / Completed

CompletedNCT03226106

Optimizing Physical Activity Outcomes After Total Knee Arthroplasty

Optimizing Physical Activity Outcomes for Veterans After Total Knee Arthroplasty

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
114 (actual)
Sponsor
VA Office of Research and Development · Federal
Sex
All
Age
50 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Although total knee arthroplasty is an effective intervention for decreasing knee pain and improving physical function, physical activity levels remain low up to a year after surgery. This study will use mobile-health technology to deliver an intervention designed to improve physical activity behavior for Veterans recovering from total knee arthroplasty. The study will assess the effectiveness of using behavior-change intervention as a supplement to conventional rehabilitation to improve physical activity. The intervention will be delivered using home-based tablet computers for Veterans to have remote interaction with the researcher and real-time physical activity feedback from a wrist-worn activity sensor.

Detailed description

This randomized clinical trial will assess the efficacy of using physical activity behavior change intervention for Veterans recovering from total knee arthroplasty. Testing will occur at baseline (before surgery), at intervention midpoint (8 weeks after surgery), end of intervention (14 weeks after surgery), and 24 weeks after intervention. The primary outcome is accelerometer-assessed daily step count. Secondary outcomes include the percent time engaged in standing and walking activity and physical function (Six-Minute Walk, 30-Second Chair-Stand Test, Timed Up-and-Go, Western Ontario and McMaster Universities Osteoarthritis Index, and the Veterans RAND 12-Item Health Survey.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPhysical Activity Behavior InterventionHome-based weekly sessions (30 min) using behavior change methods for promoting physical activity. Sessions will occur using home-based computer tablets for real-time video interface between the participant and researcher. Participants will wear wrist-mounted activity sensors with direct physical activity feedback during the intervention period to allow for behavioral feedback and action planning.
OTHERAttention ControlConventional rehabilitation with supplemental 10 telerehabilitation sessions that match the frequency and duration of the experimental arm. Attention control intervention provided as 10 telerehabilitation sessions of non-physical activity related education-only sessions.

Timeline

Start date
2017-11-15
Primary completion
2023-05-15
Completion
2023-05-15
First posted
2017-07-21
Last updated
2024-10-16
Results posted
2024-10-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03226106. Inclusion in this directory is not an endorsement.