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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02911389
Other study ID # 16Chen01
Secondary ID
Status Recruiting
Phase N/A
First received September 15, 2016
Last updated September 19, 2016
Start date March 2016

Study information

Verified date September 2016
Source Rothman Institute Orthopaedics
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if unsupervised, home rehabilitation delivered by a web-based platform or paper manual is a safe and effective alternative to outpatient physical therapy after total knee replacement.


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date March 2017
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Any patient undergoing unilateral, primary TKA

Exclusion Criteria:

1. Patients without access to the Internet

2. Patients without access to outpatient PT

3. Revision or conversion TKA

4. Patients discharged to a rehabilitation unit or other form of respite care such as a skilled nursing facility, acute rehabilitation center, convalescent home, long-term care facility or nursing home.

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Other:
Home PT via web-based platform

Home PT via paper manual

outpatient PT


Locations

Country Name City State
United States Rothman Institute Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Rothman Institute Orthopaedics

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Knee Range of Motion Measured in degrees from 0-130 1 month post surgery No
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