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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03922737
Other study ID # 2019Horneff
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date October 6, 2017
Est. completion date December 1, 2019

Study information

Verified date April 2019
Source Rothman Institute Orthopaedics
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to evaluate the quality of care provided by a home-based teleheath program as a safe and acceptable alternative to an in-person office visit as determined by satisfaction with the program and the amount of further medical management required by the patients.


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Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
In-person office visit
Post-operative visit to occur in-person with provider
Teleheath visit
Post-operative visit to occur via telehealth software platform with provider

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 Patient Satisfaction: Likert Score Likert Score self-reported patient satisfaction 2 mont post-operative period following surgery
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