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NCT04302077 Clinical Trial

Patient Satisfaction With Virtual Post Operative Visits: Hip Arthroscopy

Femoroacetabular Impingement Clinical Trial

Official title:
Patient Satisfaction With Virtual Post Operative Visits: Hip Arthroscopy

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04302077
Other study ID # 19-01949
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 15, 2020
Est. completion date May 1, 2021

Study information
Verified date January 2022
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a prospective, randomized study designed to evaluate the effects of different initial postoperative follow-up modalities. Given the nature of the study, it is not possible for either the surgeons or the subjects to be blinded. Patients will be assigned to either group based on the last digit of their medical record number (MRN). Patients with an even-ending medical record number will be randomized to virtual visit/telemedicine, while patients with an odd-ending medical record number will be randomized to the office visit.

Description:

This study aims to evaluate the differences between two forms of postoperative follow-up with respect to patient satisfaction. The primary outcome will be patient satisfaction with their surgeon and with their overall experience. Following their second postoperative visit, the subjects will complete one electronic survey. The survey is designed to assess subject's overall satisfaction and satisfaction with their surgery. This survey is standardized and will be used by both groups.

Recruitment information / eligibility
Status Completed
Enrollment 75
Est. completion date May 1, 2021
Est. primary completion date April 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Participants undergoing arthroscopic hip surgery Exclusion Criteria: - Age < 18 years old or Age > 70 years old

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• virtual doctor visit
interactive live-video feed at home through EPIC
• Standard care doctor's visit
In person visit as per standard of care

Locations
Country Name City State
United States NYU Langone Health New York New York

Sponsors (1)
Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in patient satisfaction Participant satisfaction will be measured by a electronic survey . At the conclusion of the in-person or virtual visit, participants will be provided instructions how to access the survey questions through the QR code if in-person and through a secure link if at home via telemedicine through EPIC. 3 month follow up visit
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