Accessible Remote Rehabilitation System for Real-Time Biomechanical Monitoring

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMississippi State University

About this trial

This study evaluates a novel camera-based system designed to support remote rehabilitation by measuring hand and upper-limb biomechanics in real time. Many patients recovering from musculoskeletal or neurological conditions require frequent monitoring during rehabilitation, but regular clinic visits may be difficult due to distance, cost, or limited access to specialized care. Current telehealth approaches typically rely on qualitative assessments or self-reported feedback rather than objective biomechanical measurements.

The purpose of this study is to determine whether a computer vision-based system can accurately estimate biomechanical parameters such as joint angles, range of motion, muscle force, and joint torque using only a standard camera. The system analyzes hand movement using artificial intelligence and biomechanical modeling to provide real-time measurements during rehabilitation exercises.

Participants will perform guided hand-movement tasks while the system records video and extracts anatomical landmarks. These data will be used to compute biomechanical parameters and assess whether the system can reliably monitor rehabilitation progress remotely. The results will help determine whether this technology can provide clinicians with objective, continuous data to support personalized rehabilitation and improve patient outcomes.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adults aged 18 years or older.

Individuals undergoing or recovering from upper-limb or hand rehabilitation following musculoskeletal or neurological injury or surgery.

Ability to perform basic hand or upper-limb movement tasks required for the rehabilitation exercises.

Ability to understand study instructions and provide informed consent.

Disqualifiers

Severe cognitive impairment preventing understanding of study procedures.

Medical conditions that prevent safe participation in hand or upper-limb rehabilitation exercises.

Severe visual impairment preventing interaction with the camera-based monitoring system.

Participation in another interventional study that could affect rehabilitation outcomes.

Trial design

Design model

Parallel

Treatments tested in this trial

  • AI-Based Camera Tele-Rehabilitation Monitoring System

    Device

    A single-camera, computer vision and inverse-dynamics modeling system that estimates biomechanical parameters (joint torque, muscle force, and range of motion) from video-based hand landmark tracking during rehabilitation exercises.

  • Standard Telehealth Rehabilitation

    Behavioral

    Participants perform standard rehabilitation exercises and receive routine telehealth follow-up with clinicians according to usual care practices. No camera-based biomechanical monitoring system is used during the rehabilitation process.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Camera-Based Biomechanical Monitoring (Intervention)Experimental treatment 1 intervention
Group B: Standard Telehealth Rehabilitation (Control)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Accuracy of Camera-Based Joint Torque Estimation

Accuracy of the AI-based camera system in estimating joint torque during rehabilitation exercises compared with gold-standard dynamometer measurements. Accuracy will be evaluated using mean absolute percentage error (MAPE) between estimated torque values and reference dynamometer readings.

Time frame
Baseline assessment session
2

Correlation Between Camera-Based and Clinical Biomechanical Measurements

Agreement between biomechanical parameters estimated by the camera-based system and reference clinical measurements. Pearson correlation coefficients and Bland-Altman analysis will be used to evaluate agreement between estimated joint torque and gold-standard measurements.

Time frame
Baseline assessment session

Secondary outcomes

1

Grip Strength Improvement

Change in hand grip strength measured using a clinical dynamometer during the rehabilitation program.

Time frame
Baseline, 3 weeks, and 6 weeks
2

Range of Motion Improvement

Change in hand and finger joint range of motion measured using standard clinical goniometry during the rehabilitation period.

Time frame
Baseline, 3 weeks, and 6 weeks
3

Functional Recovery Time

Time required for participants to regain at least 80% of their pre-injury hand function based on clinical functional assessments.

Time frame
Up to 6 weeks
4

Patient Adherence to Rehabilitation Exercises

Participant adherence to prescribed rehabilitation exercises measured by completion rate of assigned therapy sessions during the study period.

Time frame
Up to 6 weeks

Other outcomes

Sponsors and contacts

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Mississippi State University

Lead sponsor

University of Mississippi Medical Center

Collaborator

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