Conventional and Virtual Reality-Based Neuromuscular Rehabilitation in Scapholunate Instability

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorYeditepe University

About this trial

Scapholunate instability is a common form of carpal instability that can cause wrist pain, weakness, and functional limitations during daily activities. Conservative rehabilitation approaches are frequently recommended in the early stages; however, there is no standardized rehabilitation protocol, and the effects of different neuromuscular rehabilitation methods have not been sufficiently investigated.

The primary aim of this study is to comparatively examine the effects of conventional physiotherapy approaches and virtual reality-supported neuromuscular rehabilitation on forearm muscle activation patterns assessed using surface electromyography, wrist proprioceptive function (joint position sense), pain intensity, and functional improvement in individuals with scapholunate instability, and to identify clinically applicable rehabilitation protocol approaches for this population.

In this single-blind randomized controlled trial, participants with pre-dynamic or dynamic scapholunate instability will be randomly assigned to either a conventional rehabilitation group or a virtual reality-supported rehabilitation group. Both groups will receive an 8-week rehabilitation program administered twice per week. Primary outcome measures will include electromyographically assessed forearm muscle activation and wrist proprioception. Secondary outcome measures will include pain intensity, grip strength, wrist muscle strength, and upper extremity functional outcomes assessed using validated clinical instruments. All outcome assessments will be performed before and after the intervention period by an assessor blinded to group allocation.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged between 18 and 65 years

Diagnosed with scapholunate instability (pre-dynamic or dynamic instability) by a physician and referred for conservative treatment

A score of ≤6 on the Beighton Hypermobility Scale

Presence of clinical instability symptoms, including pain, a sense of instability, and functional limitation

Disqualifiers

History of previous surgery involving the hand or wrist

Presence of any neurological or cardiovascular disorder

Presence of additional orthopedic pathology affecting the shoulder, elbow, or wrist other than scapholunate instability

History of surgery involving the ipsilateral upper extremity within the past 6 months

Trial design

Design model

Parallel

Treatments tested in this trial

  • Conventional Physiotherapy Group

    Other intervention

    Participants assigned to the conventional physiotherapy group will receive a structured neuromuscular rehabilitation program focusing on wrist and forearm stabilization. The intervention will include supervised strengthening exercises targeting scapholunate-friendly muscles, neuromuscular control exercises, and proprioceptive training aimed at improving wrist stability and functional movement patterns. Progressive resistance and task-oriented exercises will be used according to individual tolerance. The rehabilitation program will be administered twice per week for 8 weeks by a licensed physiotherapist.

  • Virtual Reality-Supported Neuromuscular Rehabilitation

    Other intervention

    Participants in the virtual reality-supported rehabilitation group will receive the same conventional physiotherapy program as the control group. In addition, this group will participate in virtual reality-based therapeutic exercises delivered through sensor-based interactive games designed for upper extremity rehabilitation. These exercises will aim to enhance wrist and forearm motor control, proprioceptive feedback, and functional task performance by promoting controlled and task-oriented movement patterns. Virtual reality sessions will be supervised by a physiotherapist and integrated into the rehabilitation program with the same frequency and duration as the conventional intervention, administered twice per week over an 8-week period.

Treatment groups

36 Participants
are divided into 2 treatment groups
Group A: Conventional Physiotherapy GroupActive comparator 1 intervention
Group B: Virtual Reality-Supported Neuromuscular Rehabilitation GroupExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Wrist Proprioception

Wrist proprioception will be assessed by evaluating joint position sense using both a universal goniometer and an electrogoniometer. Assessments will be performed in a standardized sitting position with the forearm supported. Predetermined wrist joint angles will be set by the assessor, and participants will be asked to actively reproduce the target positions without visual feedback. Wrist joint angles will be recorded using both measurement tools, and the absolute angular error between the target angle and the reproduced angle will be calculated to determine proprioceptive accuracy.

Time frame
Baseline and after 8 weeks of intervention
2

Forearm Muscle Activation

Forearm muscle activation will be assessed using surface electromyography during standardized wrist and forearm tasks. Electromyographic activity of selected forearm muscles involved in wrist stabilization will be recorded and analyzed to evaluate neuromuscular activation patterns.

Time frame
Baseline and after 8 weeks of intervention

Secondary outcomes

1

Pain Intensity

Pain intensity will be assessed using the Visual Analog Scale (VAS). Participants will rate their wrist pain on a 10-cm horizontal line, where higher scores indicate greater pain intensity.

Time frame
Baseline and after 8 weeks of intervention
2

Pressure Pain Threshold

Pressure pain threshold will be measured using a pressure algometer applied to predefined and standardized anatomical sites around the wrist. Gradually increasing pressure will be applied perpendicular to the skin at a constant rate, and participants will be instructed to indicate the point at which the sensation first becomes painful. The pressure value at this point will be recorded as the pressure pain threshold, with higher values indicating lower pain sensitivity.

Time frame
Baseline and after 8 weeks of intervention
3

Grip Strength

Grip strength will be measured using a hand dynamometer under standardized testing conditions. Participants will be seated with the shoulder adducted, elbow flexed at 90 degrees, and the forearm in a neutral position. Each participant will be instructed to perform a maximum voluntary grip contraction. Three consecutive measurements will be taken, and the highest value will be recorded to evaluate changes in hand strength.

Time frame
Baseline and after 8 weeks of intervention
4

Wrist Muscle Strength

Wrist muscle strength will be assessed using standardized strength testing of wrist flexion, extension, radial deviation, and ulnar deviation. Strength measurements will be performed in a standardized sitting position with the forearm supported, and resistance will be applied manually by the assessor. Participants will be instructed to perform maximum voluntary contractions for each movement, and the obtained strength values will be recorded to evaluate changes in wrist strength following the intervention.

Time frame
Baseline and after 8 weeks of intervention

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Yeditepe University

Lead sponsor

Biruni University

Collaborator

The Scientific and Technological Research Council of Turkey

Collaborator