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Virtual Phone Visits for Post-Operative Follow-Up at a Sports Medicine Clinic
N/A
Waitlist Available
Led By John P Andrawis, M.D.
Research Sponsored by Jonathan Wu
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up after 6 week post-operative visit, 12 week post-operative visit, and 6 month post-operative visit
Awards & highlights
Study Summary
This trial will compare how patients feel about virtual vs. in-person post-op visits. Hypothesis: PRO & satisfaction scores differ between the two groups.
Eligible Conditions
- Orthopedic Disorders
- Surgery
- Patient Satisfaction
- Sports Injuries
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ after 6 week post-operative visit, 12 week post-operative visit, and 6 month post-operative visit
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~after 6 week post-operative visit, 12 week post-operative visit, and 6 month post-operative visit
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Patient-Reported Outcomes Measurement Information System Global survey scores
Secondary outcome measures
Knee injury and Osteoarthritis Outcome Score for Joint Replacement
Patient satisfaction scores
Quick Disabilities of the Arm, Shoulder, and Hand survey scores
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: virtual phone appointment visitsExperimental Treatment1 Intervention
Randomly selected participants will receive virtual telemedicine post-operative appointment visits at 6 week, 12 week, and 6 months after surgery.
Group II: standard in-person appointment visitsActive Control1 Intervention
Randomly selected participants will receive standard in-person post-operative appointment visits at 6 week, 12 week, and 6 months after surgery.
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Who is running the clinical trial?
Jonathan WuLead Sponsor
John P Andrawis, M.D.Principal InvestigatorLundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- Adults with any type of cognitive impairment.
Research Study Groups:
This trial has the following groups:- Group 1: standard in-person appointment visits
- Group 2: virtual phone appointment visits
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is this experiment accepting new participants at the present time?
"As reported on clinicaltrials.gov, this medical experiment is no longer actively recruiting patients as it has not been updated since August 10th 2023. However, there are still 397 other studies that require participants to join their trials at the present time."
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