Evaluation of Home-based Telerehabilitation Platform to Augment Orthopedic Rehabilitation
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Software as a Medical Device (WizeCare).
- Who it may be relevant to
- Registry conditions: Anterior Cruciate Ligament Reconstruction Rehabilitation. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Device Software as a Medical Device (WizeCare)
Telehealth services will be provided through a telerehabilitation platform with AI capabilities and markerless motion capture.
Primary outcome measures
- Time to initial physical therapy visit [Time frame: At study completion, average 1 year]
- Time to first physical therapy visit scheduled [Time frame: At study completion, average 1 year]
- Number of major adverse events reported from telehealth physical therapy services [Time frame: Through study completion, an average of 1 year]
- Number of Scheduled physical therapy visits completed by enrolled patients [Time frame: At study completion, average 1 year]
- Number of participants' surveys that report satisfaction with telehealth services [Time frame: At study completion, average 1 year]
- Number of providers' surveys that report satisfaction with telehealth application use [Time frame: At study completion, average 1 year]
Secondary outcome measures (2)
- Lower Extremity Functional Scale [Time frame: Through study completion, an average of 1 year]
- Operative lower extremity pain [Time frame: Through study completion, an average of 1 year]
Eligibility criteria
Inclusion criteria
- Patients that are candidates for anterior cruciate ligament reconstruction.
Exclusion criteria
- 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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Other
Study locations
United States · 1 center
- The University of Mississippi Medical Center — Jackson
Identifiers
NCT: NCT06973642 · UMMC-IRB-2024-178 · 6 U66RH31459-06-01