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NCT Number: NCT06973642

Evaluation of Home-based Telerehabilitation Platform to Augment Orthopedic Rehabilitation

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.

Recruiting

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Key information

Conditions

Anterior Cruciate Ligament Reconstruction Rehabilitation

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University of Mississippi Medical Center

Jackson, Mississippi, 39216, United States

Location status: Recruiting

Location contact

Jacob Daniels

CONTACT

[email protected]

6018154038

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Software as a Medical Device (WizeCare)

Device

Telehealth services will be provided through a telerehabilitation platform with AI capabilities and markerless motion capture.

Primary outcomes

  1. Time to initial physical therapy visit

    Time frame: At study completion, average 1 year

    Number of days from the time the patient is enrolled in the study until the time they have their first physical therapy visit

  2. Time to first physical therapy visit scheduled

    Time frame: At study completion, average 1 year

    Number of days from when the patient is enrolled to when their first physical therapy visit is scheduled

  3. Number of major adverse events reported from telehealth physical therapy services

    Time frame: Through study completion, an average of 1 year

    Numerical count of how many major adverse events patients or providers report

  4. Number of Scheduled physical therapy visits completed by enrolled patients

    Time frame: At study completion, average 1 year

    Number of scheduled physical therapy sessions completed by patients compared to number of sessions scheduled

  5. Number of participants' surveys that report satisfaction with telehealth services

    Time frame: At study completion, average 1 year

    Participants will complete surveys after each telehealth session. Number of participants' surveys that report satisfaction compared to dissatisfaction will be measured.

  6. Number of providers' surveys that report satisfaction with telehealth application use

    Time frame: At study completion, average 1 year

    Providers will complete surveys after each telehealth session. Number of providers' surveys that report satisfaction compared to dissatisfaction will be measured.

Secondary outcomes

  1. Lower Extremity Functional Scale

    Time frame: Through study completion, an average of 1 year

    Lower Extremity Functional scale is a questionniare designed to assess functional status in patients with Lower extremity problems. The scale is 0-80 with a higher score demonstrating higher functional status

  2. Operative lower extremity pain

    Time frame: Through study completion, an average of 1 year

    Pain in relation to the lower extremity that has undergone ACL reconstructive surgery will be measured on a 0-10 scale with 0 being no pain and 10 being worse pain.

Study contacts

Contact information is provided by the study sponsor or research team.

Jacob Daniels, DPT, EdD

CONTACT

[email protected]

6018154038

Sponsors and collaborators

Lead sponsor

University of Mississippi Medical Center

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 15, 2025
Registry last updated
Jul 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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