Patient Satisfaction With Virtual Postoperative Visit

Not Applicable

Completed

• Conditions: Post-Op Complication
• Interventions: Behavioral: Traditional; Behavioral: Virtual

• Registration Number: NCT04108442
• Lead Sponsor: NYU Langone Health

Brief 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. To reduce bias that may occur due to each surgeon's personal preference for postoperative follow-up modality, the surgeons (rather than individual subjects) will be randomized to one of two postoperative follow-up modality groups (traditional or virtual).

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2019-08-01
• Study First Submitted: 2019-08-22
• Study First Submitted QC: 2019-09-26
• Study First Posted: 2019-09-30
• Primary Completion: 2020-03-01
• Study Completion: 2020-03-01
• Status Verified: 2020-10
• Last Update Submitted: 2020-10-08
• Last Update Posted: 2020-10-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 122

Inclusion Criteria

• > 18 years old
• < 60 years old
• Undergoing knee arthroscopy procedure

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Exclusion Criteria

• < 18 years old
• > 60 years old

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Traditional	Traditional	-
Virtual	Virtual	-

Primary Outcome Measures

Name	Time	Method
Patient Satisfaction with their surgeon	6 Months	Patients will report their satisfaction with their surgical experience 6 weeks after surgery using a 10-point Likert scale, 0-"Completely Dissatisfied, 10-"Completely Satisfied"

Trial Locations

Locations (1)

NYU Langone Health; 🇺🇸 New York, New York, United States