Patient Satisfaction With Virtual Postoperative Visit

NYU Langone Health

Status: Completed

Conditions: Post-Op Complication

Treatments: Behavioral: Virtual; Behavioral: Traditional

Study type: Interventional

Funder types: Other

Identifiers

NCT04108442

19-00549

Details and patient eligibility

About

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).

Enrollment: 122 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

• < 18 years old
• > 60 years old

Trial design

Primary purpose: Supportive Care

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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122 participants in 2 patient groups

Traditional

Active Comparator group

Treatment:

Behavioral: Traditional

Virtual

Experimental group

Treatment:

Behavioral: Virtual