MOBILE: Intensive motor learning based intervention to target specific walking goals as identified using the Gait Outcome Assessment List.
Full Protocol outlining strategies available on request.
Three key principles underpin the intervention:
Principle 1: The type of task
Principle 2: The type of practice
Principle 3: The type of Feedback
Study summary
The goal of this clinical trial is to learn if a new therapy approach to improve walking ability in children with Cerebral Palsy is acceptable to the children and the families in a community setting.
The main questions we look to answer are:
1. Do the children/teens tolerate the therapy and feel that it is helpful?
2. Do the parents/ families feel the therapy helps and is easy to commit to?
3. Do the children/teens complete all their therapy sessions and assessments as planned?
The participants will trial the therapy for 30 hours over 6 weeks and will perform assessments before and after to see if they meet their goals. They will also be interviewed to see how they felt about the therapy when they finish.
Eligibility
Sex
ALL
Min age
6 Years
Max age
17 Years
Healthy volunteers
No
Inclusion Criteria:
* Primary diagnosis of Cerebral Palsy (GMFCS Levels I-III)
* Has a specific walking related goal
* Has capacity to follow instruction
* Has a primary caregiver who can support a home program
Exclusion Criteria:
* Has had surgery within 6 months of intervention start date
* Has had botox/ baclofen within 3 months of intervention start date
* Has a dual diagnosis that impacts ability to follow instruction
* Has a significant cognitive impairment
Primary outcome measure(s)
Recruitment Rate — rolling recruitment over 1.5 years Percentage of eligible numbers recruited
Adherence to Intervention — Duration of study 2 years Percentage of total hours practiced/ planned dose (30 hours)
Retention — Duration of study 2 years Percentage of recruited participants at final follow up
Adverse Events — Duration of study 2 years Measured as Yes or No with description
Fidelity to Intervention Protocol — Duration of study 2 years Checklist to measure extent of motor learning principles included in sessions
Feasibility of Outcome Measures (Participant) — Duration of study 2 years Participant experience of outcomes captured by semi-structured interviews.
Feasibility of Outcome Measures (Assessor) — Duration of study 2 years Assessor experience of outcomes captured by semi-structured interview.
Acceptability of Intervention — Duration of study 2 years Semi-structured interviews of participants and parents to capture acceptability of intervention using Framework of acceptability
Time taken to complete Outcome Measures — Duration of study 2 years Measured in Minutes
Trial sites (1)
Facility
City
Region
Status
Enable Ireland Bangla Therapy Centre
Balrath
Meath
Recruiting
More Royal College of Surgeons, Ireland trials in Ireland
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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