Patient Satisfaction With Virtual Postoperative Visit
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- NYU Langone Health
- Enrollment
- 122
- Locations
- 1
- Primary Endpoint
- Patient Satisfaction with their surgeon
Study Overview
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).
Study Design
- Study Type
- Interventional
- Allocation
- Non Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 60 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •> 18 years old
- •< 60 years old
- •Undergoing knee arthroscopy procedure
Exclusion Criteria
- •< 18 years old
- •> 60 years old
Outcomes
Primary Outcomes
Patient Satisfaction with their surgeon
Time Frame: 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"
Secondary Outcomes
No secondary outcomes reported