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The Efficacy of Targeted Training on the Postural Control and Gross Motor Function in Children With Cerebral Palsy

The Efficacy of Targeted Training on the Postural Control and Gross Motor Function in Children With Cerebral Palsy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01357954
Enrollment
28
Registered
2011-05-23
Start date
2010-06-30
Completion date
2013-06-30
Last updated
2020-08-05

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

Conditions

Cerebral Palsy

Keywords

Postural control, Targeted Training, Gross motor function, Cerebral palsy

Brief summary

The project aims to test the effectiveness and explore the possibility of performing a novel therapeutic approach, targeting to increase strength and coordination around the trunk, giving a more active and functional seating and head control in those children with cerebral palsy (CP) who are wheelchair users. The project will also try to determine the muscle physiological effect of treatment using indirect measures of strength in the spinal musculature.

Interventions

The child's regular physiotherapy

Targeted training, 5 days a week for 6 months, up to 30 minutes a day

Sponsors

Hvidovre University Hospital
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
2 Years to 15 Years
Healthy volunteers
No

Inclusion criteria

* diagnosis of CP made by a neuro-pediatric physician experienced in assessment and diagnosis of CP * GMFCS level III, IV and V, * the child cannot walk without assistance, * age 2-15 year, * no joint deformity or contracture around the Targeted joint * not a candidate for surgery or other medical treatment that affects motor skills while participating in the project * trunk control problems.

Exclusion criteria

* uncontrolled epilepsy * surgery within 12 months of the study start * Botulinum toxin within 2 months of study start * Lack of personnel resources to treat the child at their school/kindergarten

Design outcomes

Primary

MeasureTime frame
Change from baseline in Gross Motor Function Measure at 6 monthsBaseline, 6 months

Secondary

MeasureTime frame
Change from baseline in thickness of the erector spinae muscles measured with ultrasound at 6 monthsBaseline, 6 months
Change from baseline in seated sway at 6 monthsBaseline, 6 months
Degree of achievement of a goal set at baseline using a modified Goal Attainment Scale (GAS)6 months
Change from baseline in Pediatric Evaluation of Disability Inventory (PEDI)at 6 monthsBaseline, 6 months
Change from baseline in thickness of the erector spinae muscles measured with ultrasound at 12 monthsBaseline, 12 months
Change from baseline in seated sway at 12 monthsBaseline, 12 months
Change from baseline in Gross Motor Function Measure at 12 monthsBaseline, 12 months
Change from baseline in Pediatric Evaluation of Disability Inventory (PEDI)at 12 monthsBaseline, 12 months

Countries

Denmark

Outcome results

None listed

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