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Video-Based Games for Upper Limb Rehabilitation in Cerebral Palsy

Video-Based Games for Upper Limb Rehabilitation in Cerebral Palsy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03622970
Enrollment
30
Registered
2018-08-09
Start date
2015-03-03
Completion date
2018-08-23
Last updated
2018-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Palsy, Rehabilitation

Brief summary

The aim of the present study is to compare the effects of Neurodevelopmental Treatment (NDT)-based upper limb rehabilitation and video-game based therapy (VGBT) with Nintendo® Wii and LMC games on upper extremity functions in patients with Cerebral Palsy (CP).

Detailed description

The investigators hypothesized that VGBT using the Nintendo® Wii and LMC would be a usable tool to train manual dexterity in patients with CP as comprehensive and holistic therapy. The NDT program for both groups will be routinely applied according to each child's individual needs and included tonus regulation, support of sensation, perception and motor development for gross motor function. The two different patient-centered rehabilitation programs will be conducted with an average of one hour sessions three times a week for 8 weeks in both groups. The two different patient-centered programs will be as VGBT with Nintendo® Wii and LMC games (Group I) and NDT-based upper limb rehabilitation (Group II).

Interventions

DEVICEVGBT with Nintendo® Wii and LMC games

Nintendo Wii and LMC games will be used for upper limb rehabilitation in Cerebral Palsy. The games are tennis and boxing for Nintendo Wii, Leapball and CatchApet for LMC.

BEHAVIORALNDT-based upper limb rehabilitation

NDT-based upper limb rehabilitation includes using real materials (clothes, spoons, pencils, buttons, rope, etc.) such as getting dressed and eating etc. Also, It will practised with the materials such as velcro cylinders, skill cubes, exercise bands, screw sets, therapeutic putty, and tripled coordination tools.

Sponsors

Istanbul University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
5 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

The health committee report has received a CP diagnosis * Being between 5-18 years of age * According to Modifiye Ashworth Scale (MAS), upper extremity spasticity (0), (1), (1+) * Ability to adapt to exercises (According to the health report mental level normal or mild mental retardation

Exclusion criteria

* Botulinium Toxin (BOTOX) injection for the upper extremity in the last 6 months * Does not have epileptic epilepsy * Any person who has been diagnosed as having any absence of a cardiac or orthopedic condition * Admission of family treatment

Design outcomes

Primary

MeasureTime frameDescription
Minnesota Hand Dexterity TestChange from baseline to 8 weeks, follow up at two monthsMinnesota Manual Dexterity Test (MMDT): is a short version of the Minnesota Dexterity Tests and consists of two timed sub-tests (placing and turning tests) to assess the required manual dexterity to turn and/or place 60 short, round blocks with one or both hands . In this study, the placing sub-test will be used to assess the ability to handle objects, measured by the time required to complete the task.

Secondary

MeasureTime frameDescription
Modified Ashworth ScaleChange from baseline to 8 weeks, follow up at two monthsModified Ashworth Scale (MAS) measures the muscle spasticity rate (score, 0-5). Spasticity of wrist flexors, elbow flexors and forearm pronators will be assessed due to MAS in this study. Participants sat with their forearm fully supported and will be instructed to relax. The measurer moves the wrist into extension as fast as possible and then rated the quality of the muscle reaction to stretch on a scale from 0 to 5, with 0 representing no spasticity.
Hand and pinch gripsChange from baseline to 8 weeks, follow up at two monthsGrip strength was measured using a standard adjustable handle Jamar® Plus+Hand Dynamometer (Irvington NY, USA) in the sitting position with the shoulder adducted and neutrally rotated and the elbow flexed at 90. Pinch strengths (tip, key and palmar pinch) will be measured by a hydraulic pinch gauge (Irvington NY, USA) in the sitting position with the shoulder adducted and neutrally rotated and the elbow flexed at 90. Pinch positions will be defined using the American Society for Hand Therapists guideline. Each of grip and pinch strength tests will be performed thrice with a 30-sec interval between tests, and the mean value will be recorded.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026