Cerebral Palsy
Conditions
Keywords
single blinded, randomised, controlled, physiotherapy, children, cerebral palsy
Brief summary
This study's main aim is to look at targeted strength training for muscles at the hips. Specifically to consider whether targeted strength training not only effects strength of the specific muscles but also ability to stand on one leg (single leg balance) as well as walking in children with cerebral palsy? This study is a feasibility of method of investigation.
Detailed description
This study is focusing on functional change. The reasoning is that if the targeted strength training is effective at improving hip muscle contribution to stability then single leg balance may be improved. This may be functionally evident when weight bearing is taken by say the left leg in gait (percentage stance phase of gait) and as a consequence the opposing swing phase will be optimised as measured by stride. Thus the research question is does strengthening of the rotating and sideways moving hip muscles improve the walking of children with CP as measured by appropriate aspects of gait? Secondly, does this targeted strengthening also increase duration of single leg balance which is a simple easy to use measure in the community without the need for specialised equipment? The primary outcome measure will use a laboratory based 4 camera Codsmotion (CODA) biomechanical analysis system to measure stride (a) and percentage duration of stance phase of gait (b). Secondarily the duration of single leg balance in terms of seconds will be recorded. Gross motor functional and quality of life as also being assessed. The intervention is strengthening which will be implemented with the principles of progressive resistance training. Children with CP's therapists would ask for this type of intervention to be carried out
Interventions
OTHERUsual care plus progresive resistance training
Duration 8 weeks; two weeks of familiarisation with the intervention protocol without resistance (for familiarisation and neural adaptation) followed by 6 weeks progressive resistance (PR). The three times a week PR training will be as a home exercise program with fortnightly home visits to monitor/progress PR training. It comprises a 4 minute warm up and cool down with one exercise targeting the hip abductors and one the lateral rotators. Exercise prescription will follow existing guidelines for progressive PR training. Parents will be taught supervision by the researcher using clear explanations in words and pictures in a logbook. Logbooks have been found to facilitate compliance, dosage and motivation.
Sponsors
University of Nottingham
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
7 Years to 16 Years
Healthy volunteers
No
Inclusion criteria
* Children with CP aged between 7-16 years having sufficient cognition to undertake a strength training program
Exclusion criteria
1. non-ambulation children or those unable to walk 5 meters independently (without walking aid), 2. lower limb surgery within 12 months, 3. botox within 6 months, 4. oral muscle relaxant medication 5. significant learning difficulty 6. Any concurrent condition which would be contraindicated to progressive resistance training such as unmanaged high blood pressure, cardiac pathology or uncontrolled epilepsy 7. Where at baseline assessment finds no weakness in the muscles under investigation 8. concurrent or within 6 months involvement in any other research study 9. Non consent to General Practitioner (GP) notification.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Gait parameter | baseline, plus 8 weeks and plus 8 weeks (exit point) | 4 camera CODA gait analysis system for change in percentage stance phase of gait and stride in cm. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Gross Motor Function Measure (GMFM) | Baseline, plus 8 weeks and plus 8 weeks (exit) | To investigate any change in dimensions D and E of fucntioal activity with standardised GMFM. |
Countries
United Kingdom
Contacts
Primary ContactSarah E Westwater-Wood, MMedSci, BSc
Backup ContactGrahame Pope, MPhil, BSc
Outcome results
None listed