Effect of Using an Object Handling Serious Game on Upper Limb Rehabilitation for Children with Neurological Disorders

NCT06866730 | Recruiting

• 1 other identifier: REPLAY
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 2

Brief Summary

Cerebral palsy, and more broadly neurological disorders, can lead to significant motor impairments that impact individuals' daily lives. To address these limitations, the French National Authority for Health has issued recommendations for rehabilitative care, highlighting intensive training programs, physical activity, and interactive computer games. Scientific literature has also demonstrated the benefits of therapies that incorporate repetition. In this study, the investigators aimed to train patients in producing grasp-and-release movements, and more broadly \*reach-to-grasp\* actions, in a manner intensified by movement repetition. To mitigate the boredom inherent to such repetitive tasks, the invesigators developed a device resembling a serious game, equipped with software, a modular physical platform, and two instrumented figurines designed to interact with the software. Intensive therapy through repetitive movements, supported by the engaging nature of serious games, is expected to improve the manual skills of children with neurological disorders causing motor impairments. To test this hypothesis, a cohort of 5 to 10 children aged 4 to 17 years with neurological disorders causing motor impairments will be invited to participate in the protocol. Participants will first undergo a baseline assessment, which will include repeated measurements of their score on the \*Box and Blocks Test\* and the active range of motion (AROM) of the wrist in extension and supination. An \*Assisting Hand Assessment (AHA)\* test will also be conducted. Following this, a 4-week intervention will be implemented, consisting of three 40-minute sessions per week. During these sessions, the child will play the game and complete the \*Box and Blocks Test\* as well as active range of motion assessments. In total, approximately 4 hours of gameplay is estimated over the course of the intervention, which will conclude with a repeat of the AHA test. A follow-up assessment will take place two months after the intervention's end, with a single measurement of the three parameters (\*Box and Blocks Test\*, AROM, and AHA).

Conditions

Neurologic Disorder

Outcome Measures

Primary Outcomes (1)

• Box and Blocks test

  Participant must transfer, one by one, with one hand, a maximum number of cubes from one side to the other of the box in 1 minute. A higher score represents better performance.

  3 months

Secondary Outcomes (2)

• Active Range of Motion

  3 months

• Assisting Hand Assessment

  3 months

Study Arms (1)

Serious game upper limb rehabilitation

EXPERIMENTAL

4 weeks program with 3 sessions per week of 40 minutes of serious game to improve upper limp motor function

Device: Serious game

Interventions

Serious game DEVICE

Serious game in which participants manipulate instrumented toys

Serious game upper limb rehabilitation

Eligibility Criteria

• Age: 4 Years - 17 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)

You may qualify if:

• Neurological disorder causing motor impairment
• Age 4 to 17 years old
• MACS level I to III
• Ability to cooperate, understand, and follow simple instructions to play the game.
• Patient affiliated with the French social security system.
• Voluntary patient whose parents have given consent for their child to participate in the study.

You may not qualify if:

• A diagnosis of photosensitive epilepsy mentioned in the medical record AND/OR a note in the child's medical record or reported by the parents of a history of seizures triggered by video game use.
• Botulinum toxin treatment within the 3 months prior to the study or intensive rehabilitation of manual skills (e.g., mCIMT, HABIT, etc.).
• Sensory and/or cognitive impairments that would interfere with playing the game.

Sponsors & Collaborators

• Fondation Ellen Poidatz: lead

Study Sites (2)

CRMTP Elisatbeth de la Panouse-Debré

Antony, 92160, France

RECRUITING

Fondation Ellen Poidatz

Saint-Fargeau-Ponthierry, 77310, France

RECRUITING

MeSH Terms

Conditions

Nervous System Diseases

Central Study Contacts

Eric Desailly, Ph.D.

CONTACT

+33 1 60 65 27 65; eric.desailly@fondationpoidatz.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: Single Case Experimental Design

Study Record Dates

• First Submitted: November 18, 2024
• First Posted: March 10, 2025
• Study Start: November 12, 2024
• Primary Completion (Estimated): September 1, 2026
• Study Completion (Estimated): September 1, 2026
• Last Updated: March 13, 2025

Record last verified: 2025-03

Locations

FR (2)