Patient Satisfaction With Virtual Postoperative Visit

Post-Op Complication Clinical Trial

Official title:

Patient Satisfaction With Virtual Postoperative Visit

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04108442
• Other study ID #: 19-00549
• Status: Completed
• Phase: N/A
• Start date: August 1, 2019
• Est. completion date: March 1, 2020

Study information

• Verified date: October 2020
• Source: NYU Langone Health
• Contact: n/a
• Is FDA regulated: No
• 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. 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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 122
• Est. completion date: March 1, 2020
• Est. primary completion date: March 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• > 18 years old

• < 60 years old

• Undergoing knee arthroscopy procedure

Exclusion Criteria:

• < 18 years old

• > 60 years old

Related Conditions & MeSH terms

• Post-Op Complication
• Postoperative Complications

Intervention

Behavioral:
• Traditional
Surgeons (rather than individual subjects) will be randomized to traditional Postoperative follow-up modality groups. They will adhere to this form of postoperative follow-up for all of their surgical patients (subjects) for one month.
• Virtual
Surgeons (rather than individual subjects) will be randomized to virtual postoperative follow-up modality group. They will adhere to that form of postoperative follow-up for all of their surgical patients (subjects) for one month.

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	Patient Satisfaction with their surgeon	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"	6 Months