Actively Recruiting
Evaluation of Home-based Telerehabilitation Platform to Augment Orthopedic Rehabilitation
Led by University of Mississippi Medical Center · Updated on 2025-07-24
15
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this study is to assess the feasibility of utilizing a telehealth rehabilitation platform to increase patient access for individuals who have undergone orthopedic surgery. Patient participants will be seen via telehealth until they are able to be seen by an in-person physical therapist of their choice. Provider participants will be the physical therapist who are providing physical therapy services through the telehealth application. Data collection: Patient and provider post surveys Home program and scheduled visit compliance rate Healthcare information in keeping with Stand of care physical therapy practices Feasibility criteria will be assessed to determine whether this modality improves physical therapy access for patients living in rural areas.
CONDITIONS
Official Title
Evaluation of Home-based Telerehabilitation Platform to Augment Orthopedic Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients that are candidates for anterior cruciate ligament reconstruction.
You will not qualify if you...
- Visual impairment greater than 20/200 with the use of corrective lenses
- Does not own or have consistent access to a phone with data capabilities
- Has been informed by their healthcare provider that they should not participate in physical therapy services
- Participants can be excluded from the study at any time if the physical therapist determines the patient is not an appropriate candidate for telehealth therapy.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The University of Mississippi Medical Center
Jackson, Mississippi, United States, 39216
Actively Recruiting
Research Team
J
Jacob Daniels, DPT, EdD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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