- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06170814
Effects of Different Focuses of Attention on Walking and Balance in Children With Cerebral Palsy
Investigation of the Effects of Different Focuses of Attention on Functional Walking and Balance in Children With Cerebral Palsy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In the external focus of attention (EF), attention is directed to movement and an environmental stimulus. In the internal focus (IF), attention is directed directly to body movements. In revealing positive effects in external focus; Methods such as metaphor, analogy, imaginary objects, mental analogies can be used. Adopting an External focus of attention (focusing on the effects of movements on the object or environment), as opposed to an Internal focus of attention (focusing on body movements), has been found to significantly improve performance on a variety of tasks. Walking and balance are essential for activities of daily living and social participation; Therefore, it is often considered one of the most important activities in daily life. Walking and balance is an automatic rhythmic motor behavior controlled mostly by subcortical brain regions. Automaticity means that walking can be performed without requiring attention. Although it seems like a very simple activity, it is actually a very complex chain of movements in which the brain, spinal cord, muscles, bones and joints work together in coordination. However, movement, balance and gait disorders cause individuals with CP to spend more energy, deteriorate their mobility and decrease their independence. Although the beneficial effects of EF have not yet been demonstrated for every population, the constrained action hypothesis encourages the use of an EF for teaching motor skills. Looking at the literature, the effects of EF on the development of motor performance in children with cerebral palsy have not been examined. Therefore, this study aims to examine the effects of external focus of attention on gait and balance.
Individuals with CP between the ages of 6-18 will be included in the research. After the purpose and scope of the study are explained to all individuals and their families who agree to participate in the study, their families will be asked to read and sign the volunteering form. All individuals who meet the inclusion criteria will be randomly divided into 2 groups (external focus and internal focus). It was planned to include 24 individuals in total, 12 individuals in each group. The same evaluations will be made to all individuals participating in the study by a physiotherapist who is an expert in the field. In addition to conventional physiotherapy for 6 weeks, individuals will be included in an exercise program that focuses on external and internal attention for 30 minutes a day, 3 days a week. Evaluation of walking function will be done with the C-Mill Walking Training System. Balance function will be performed by standing on one leg, pediatric berg balance scale and functional reaching tests.Independence Pediatric Functional Independence Scale will be evaluated with.Trunk control, trunk control measurement scale will be evaluated with.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Ankara, Turkey
- Rabia ERASLAN
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Children with hemiparatic cerebral palsy between the ages of 6 and 18 will be included in the study.
In order to perceive the commands during the exercise, the children participating in the study must have a level of cognitive development to be cooperative.
Description
Inclusion Criteria:
- Being diagnosed with spastic type cerebral palsy between the ages of 6-18
- Volunteerism of the family and individuals to participate in the study
- Being at levels I and II according to the Gross Motor Classification System
- Having the cognitive development to be cooperative
Exclusion Criteria:
- Having undergone any orthopedic and/or neurological surgery in the last 6 months,
- Having hearing and/or vision loss that would prevent participation in the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
external odak
Exercise will be done for approximately 40 minutes, 3 days a week for 6 weeks.
Ramps, obstacle jumping, stairs and tracks will be built to improve walking and balance functions.
During exercises, attention is directed to movement and an environmental stimulus in the external focus of attention.
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Exercise will be done for approximately 40 minutes, 3 days a week for 6 weeks.
Ramps, obstacle jumping, stairs and tracks will be built to improve walking and balance functions.
One group will be given external focus stimuli, the other group will be given internal focus stimuli.
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|
internal focus
Exercise will be done for approximately 40 minutes, 3 days a week for 6 weeks.
Ramps, obstacle jumping, stairs, and tracks will be built to improve walking and balance functions.
In internal focus during exercises, attention is directed directly to body movements.
|
Exercise will be done for approximately 40 minutes, 3 days a week for 6 weeks.
Ramps, obstacle jumping, stairs and tracks will be built to improve walking and balance functions.
One group will be given external focus stimuli, the other group will be given internal focus stimuli.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Gait
Time Frame: 6 week
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Walking function will be evaluated twice with the C-Mill Walking Training System, before and at the end of treatment (6 weeks of treatment).
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6 week
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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balance
Time Frame: 6 week
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Balance function will be evaluated twice, before and at the end of treatment (6 weeks of treatment), with the one-leg standing test and the functional reaching test.
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6 week
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Trunk control measurement scale
Time Frame: 6 week
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trunk control, trunk control measurement scale will be evaluated with.
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6 week
|
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Pediatric Functional Independence Scale
Time Frame: 6 week
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Independence, Pediatric Functional Independence Scale will be evaluated with.
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6 week
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pediatric berg balance scale
Time Frame: 6 week
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The Pediatric Balance Scale is a modified version of the Berg Balance Scale that is used to assess functional balance skills in school-aged children.
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6 week
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Beauchet O, Berrut G. [Gait and dual-task: definition, interest, and perspectives in the elderly]. Psychol Neuropsychiatr Vieil. 2006 Sep;4(3):215-25. French.
- Yamada M, Raisbeck LD, Porter JM. The Effects of Using Imagery to Elicit an External Focus of Attention. Res Q Exerc Sport. 2021 Sep;92(3):559-565. doi: 10.1080/02701367.2020.1733455. Epub 2020 Mar 6.
- Bunger A, Urfer-Maurer N, Grob A. Multimethod Assessment of Attention, Executive Functions, and Motor Skills in Children With and Without ADHD: Children's Performance and Parents' Perceptions. J Atten Disord. 2021 Feb;25(4):596-606. doi: 10.1177/1087054718824985. Epub 2019 Jan 30.
- Blank R, Barnett AL, Cairney J, Green D, Kirby A, Polatajko H, Rosenblum S, Smits-Engelsman B, Sugden D, Wilson P, Vincon S. International clinical practice recommendations on the definition, diagnosis, assessment, intervention, and psychosocial aspects of developmental coordination disorder. Dev Med Child Neurol. 2019 Mar;61(3):242-285. doi: 10.1111/dmcn.14132. Epub 2019 Jan 22.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Cerebral palsy and gait
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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