Home-Based Exergame Rehabilitation for Upper Limb Function in People With Multiple Sclerosis

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMarina Castel Sánchez

About this trial

This randomized pilot clinical trial aims to evaluate the effectiveness, feasibility, and cost-effectiveness of a semi-autonomous upper-limb rehabilitation program based on therapeutic exergames in people with Multiple Sclerosis (MS). The intervention integrates intensive motor practice, multisensory feedback, and cognitively demanding tasks to enhance upper-limb function, dexterity, and patient autonomy. Participants will be randomly assigned to either an exergame-based home rehabilitation program with remote physiotherapist supervision or a dose-matched conventional home-based physiotherapy program.

The primary outcome is upper-limb functionality measured by the Action Research Arm Test (ARAT). Secondary outcomes include motor function, manual ability, quality of life, usability, adherence, and digital performance metrics related to the execution of motor and cognitive tasks. Follow-up at 16 weeks will assess the sustainability of treatment effects.

This study seeks to generate evidence on whether exergame-based rehabilitation can serve as an accessible, scalable, and patient-centered alternative to conventional home-based upper-limb rehabilitation for individuals with MS.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years.

Clinical diagnosis of Multiple Sclerosis with EDSS score between 2.0 and 6.5, with upper-limb involvement.

Ability to maintain independent sitting and to stand with or without assistive devices.

Upper-limb functional capacity between 11 and 54 points on the ARAT, indicating limited to substantial impairment.

Disqualifiers

Acute illness, musculoskeletal injury, or pain interfering with the ability to perform the intervention exercises.

Uncompensated visual or hearing impairments that limit participation.

Disruptive behavior or other conditions that significantly hinder participation in the rehabilitation program.

Active epilepsy or any medical contraindication to physical exercise.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Exergame-Based Upper Limb Rehabilitation Program

    Behavioral

    Participants in the experimental group will complete a semi-autonomous home-based exergame rehabilitation program targeting upper-limb motor, sensory, and perceptual function. The intervention integrates intensive motor practice, multisensory feedback, dual-task demands, visuomotor coordination, and progressive task difficulty. Remote supervision will be provided by a physiotherapist to monitor adherence, adjust progression, and ensure safety. Dose and Schedule: 5 sessions per week 30-40 minutes per session Duration: 8 weeks Mode of Delivery: Home-based training using therapeutic exergames, with remote monitoring and session review by a physiotherapist.

  • Conventional Home-Based Physiotherapy

    Behavioral

    Participants in the control group will follow a conventional individualized physiotherapy program focused on upper-limb motor rehabilitation. The program includes strengthening exercises, functional upper-limb tasks, and repetitive practice designed to match the dose and duration of the experimental group. Dose and Schedule: 5 sessions per week 30-40 minutes per session Duration: 8 weeks Mode of Delivery: Home-based exercises with standard clinical follow-up and therapist support as needed.

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Exergame-Based Semi-Autonomous ProgramExperimental treatment 1 intervention
Group B: Conventional Physiotherapy ProgramActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Action Research Arm Test (ARAT)

The ARAT assesses upper-limb functionality across four domains: grasp, grip, pinch, and gross movement. Scores range from 0 to 57, with higher scores indicating better upper-limb function and less impairment.

Time frame
Baseline (V0), Week 8 (V1), Week 16 (V2)

Secondary outcomes

1

EuroQol EQ-5D-5L

The EuroQol 5-Dimension 5-Level Questionnaire (EQ-5D-5L) is a standardized measure of health-related quality of life. It provides (1) a utility index score, ranging from -0.281 to 1.000, where higher scores indicate better health status, and (2) a Visual Analog Scale (VAS) ranging from 0 to 100, where 0 represents the worst imaginable health and 100 represents the best imaginable health.

Time frame
Baseline, Week 8, Week 16
2

Wolf Motor Function Test (WMFT)

Assesses upper-limb motor performance through timed tasks and strength measures. Scores range from 0 to 75, with higher scores indicating better motor function.

Time frame
Baseline, Week 8, Week 16
3

Fugl-Meyer Assessment for Upper Extremity (FMA-UE)

Evaluates motor function, sensation, passive joint mobility, and joint pain. Total scores range from 0 to 66, with higher scores indicating better motor recovery.

Time frame
Baseline, Week 8, Week 16
4

ABILHAND Questionnaire

The ABILHAND Questionnaire is a patient-reported measure of perceived manual ability during bimanual activities of daily living. Each item is rated using three response categories: "impossible," "difficult," and "easy." Responses are converted through Rasch analysis into a linear measure of manual ability. The official scoring system provides Rasch-transformed results that can be expressed on a 0-100 scale, where 0 represents the lowest manual ability and 100 represents the highest manual ability.Higher scores indicate better perceived manual ability.

Time frame
Baseline, Week 8, Week 16

Other outcomes

1

Adherence to the Rehabilitation Program

Percentage of completed sessions out of the prescribed 40 sessions. Adherence ≥80% is considered adequate.

Time frame
Throughout the 8-week intervention
2

Effective Practice Dose

Total minutes of active motor or cognitive task execution, recorded by the physiotherapist.

Time frame
Each session (summed across intervention period, up to 8 weeks)
3

Movement Accuracy

Movement accuracy will be quantified as the number of correctly performed task executions recorded by the digital platform during each training session. Higher values indicate better task performance and motor control.

Time frame
During each training session during the 8week-intervention program
4

Perceived Effort (Modified Borg Scale 0-10)

Perceived effort will be assessed using the Modified Borg Scale, a validated measure of perceived exertion that ranges from 0 ("nothing at all") to 10 ("maximal").Higher scores indicate greater perceived exertion. Participants will report their perceived effort immediately after each training session.

Time frame
End of each session (up to 40 minutes)

Sponsors and contacts

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Marina Castel Sánchez

Lead sponsor

European University of Madrid

Sponsor institution

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