Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
122 participants
INTERVENTIONAL
2019-08-01
2020-03-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Traditional
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
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.
Interventions
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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.
Eligibility Criteria
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Inclusion Criteria
* \< 60 years old
* Undergoing knee arthroscopy procedure
Exclusion Criteria
* \> 60 years old
18 Years
60 Years
ALL
No
Sponsors
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NYU Langone Health
OTHER
Responsible Party
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Principal Investigators
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Kirk Campbell, MD
Role: PRINCIPAL_INVESTIGATOR
New York Langone Health
Locations
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NYU Langone Health
New York, New York, United States
Countries
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Other Identifiers
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19-00549
Identifier Type: -
Identifier Source: org_study_id
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