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N/A N=306 Randomized Supportive Care

Virtual vs. Traditional Physical Therapy Following Total Knee Replacement

Total Knee Replacement

Enrolled (actual)
306
Serious AEs
Results posted
Jan 2020
Primary outcome: Primary: Cost Difference in US Dollars — 1050.00; 2805.00 US Dollars

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Virtual physical therapy rehabilitation program (Device); No intervention (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Duke University
Primary completion
Mar 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Cost Difference in US Dollars
1050.00; 2805.00
SECONDARY
Knee Injury and Osteoarthritis Outcome Score (KOOS)
61.0; 61.8; 69.6; 67.2
SECONDARY
Range of Motion
2.5; 2.9; 114.5; 111.4
SECONDARY
10-meter Gait Speed
1.0; 1.0
SECONDARY
Pain Score
2.7; 3.0
SECONDARY
Report of Falls
19.4; 14.6
SECONDARY
Re-hospitalization
0.1; 0.2

Summary

The goals of this research study are the following: 1. To compare the effects of tele-rehabilitation-supported physical therapy versus traditional home and/or clinic-based physical therapy for total knee replacement (TKR) on 90-day health service use costs. 2. To compare tele-rehabilitation-supported physical therapy and traditional physical therapy on patient-centered outcomes 3. To explore whether individual patient characteristics are associated with differential improvement from 6 to 12 weeks assessed by patient-reported outcomes.

Eligibility Criteria

Inclusion Criteria

  • ≥ 18 years of age
  • Scheduled to have a non-traumatic TKR
  • Can be enrolled a minimum of 10 days prior to surgery (in-person visit)
  • Have a Risk Assessment and Prediction Tool (RAPT) score of ≥ 6 indicating expected discharge home after surgical hospitalization

Exclusion Criteria

  • Unable or unwilling to provide informed consent, including but not limited to cognitive or language barriers (comprehension)
  • Scheduled for staged bilateral TKR
  • Living in a nursing home prior to surgery
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02914210). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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