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Wii Fit and cerebral palsy feasibility study

A feasibility study of virtual reality as a therapeutic intervention in children with ambulatory cerebral palsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17624388
Enrollment
80
Registered
2015-03-05
Start date
2015-07-27
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Cerebral Palsy Nervous System Diseases

Interventions

1. Control Group: Control participants will use the Nintendo Wii Fit for 30-minute sessions, 3 times a week, over a 12-week period. They will have free choice over which games they cho

Sponsors

Sussex Community NHS Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for questionnaire (phase one of study): 1.1. Parents of children with cerebral palsy of any level (ie GMFCS 1-5) 1.2. Child aged 5 to 16 years old 1.3. Under management of Sussex Community NHS Trust identified from local clinical database 2. Inclusion criteria for randomised, single blind, controlled study (phase two of study): 2.1. Ambulatory Bilateral and Unilateral CP 2.2. GMFCS types I and II e.g. able to walk without a walking aid 2.3. Ability to follow simple task instruction 2.4. All school ages -from 5 up to the age of 16; primary -5 to 11 years and secondary >11 – 16 years, (Upper limit of 16 to avoid timetabling variations at 6th form programmes) 2.5. Under management of Sussex Community NHS Trust, identified from local clinical database

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for questionnaire (phase one of study): 1.1. Child aged less than 5 or over 16 years old 2. Exclusion criteria for randomised, single blind, controlled study (phase two of study): 2.1. Children who are GMFCS III, IV, V 2.2. Child/Family unable to follow simple task instructions in English 2.3. Over the age of 16, outside of school age 2.4. Child with epilepsy who is photosensitive and has had a seizure within the last year 2.5. On anticonvulsant medication

Design outcomes

Primary

MeasureTime frame
1. Gross Motor Function Measurement (GMFM) 2. Bruininks-Oseretsky test of motor proficiency (BOT-2) 3. Timed up and go test (TUG) 4. Goal Attainment Scale (GAS) 5. Strengths and Difficulties Questionnaire Measurements will be taken at baseline (week 1), midway (week 6), and exit of trial period (week 12). Measurements will be taken by blinded members of the trial team.

Countries

United Kingdom

Contacts

Public ContactWilliam Farr

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026