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Gait Analysis and Interdisciplinary Interventions for Children With Cerebral Palsy (CPinMotion)

Primary Purpose

Cerebral Palsy

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Intervention with IGA
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Palsy focused on measuring Cerebral palsy, Instrumented gait analysis, Gait Deviation Index

Eligibility Criteria

5 Years - 8 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Spastic Cerebral palsy
  • Gross Motor Function Classification System levels I or II.

Exclusion Criteria:

  • Earlier interventions in the form of orthopaedic surgery within the past 52 weeks, injection with botulinum toxin type A in the 12 weeks prior to baseline assessments
  • Relocation to another region during the trial.
  • If the child not are able to demonstrate sufficient co-operation and cognitive understanding to participate in the IGA.

Sites / Locations

  • University of Southern Denmark - Odense University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention with IGA

Intervention without IGA

Arm Description

Individually tailored interdisciplinary intervention based on measures performed as part of the Cerebral Palsy follow-Up Program and other clinical examinations AND instrumented gait analysis (IGA)

'Care as usual' - Individually tailored interdisciplinary interventions based on measures performed as part of the Cerebral Palsy follow-Up Program and other clinical examinations BUT NOT (IGA).

Outcomes

Primary Outcome Measures

Change from baseline in Gait Deviation Index
Gait Deviation Index (GDI) is based upon kinematic data from the Instrumented Gait Analysis, and is an quantitative index that summarises the overall gait pattern into a single score for each patient by comparison with non-pathological gait. A GDI value of 100 represents the absence of gait pathology, and each 10-point decrement below 100 indicates one standard deviation from normal gait kinematics. For the primary outcome measure, the median of five trials for each leg will be used to calculate the average of both legs to provide a single index for each child.

Secondary Outcome Measures

Change from baseline in 1-minute walk test
Walking performance is assessed with the 1-minute walk test. The test measure the distance in meters, when the child walks as fast as possible.
Change from baseline in Mobility Scale of the Pediatric Evaluation of Disability Inventory
The Mobility Scale of the Pediatric Evaluation of Disability Inventory evaluates the child's functional mobility in everyday activities with regard to functional skills and caregiver assistance. The Paediatric Evaluation of Disability Inventory will be applied as a parental questionnaire, allowing comparison of the child's functional skills over time for each of the two dimensions.
Change from baseline in Pediatric Quality of Life Inventory Cerebral Palsy Module
The Pediatric Quality of Life Inventory Cerebral Palsy Module is a measure of health-related quality of life, specifically designed for children with CP. The Pediatric Quality of Life Inventory Cerebral Palsy Module is based upon the parents' report and measures physical, emotional, social and school functioning.
Change from baseline in Pediatric Outcome Data Collection Instrument
The Pediatric Outcome Data Collection Instrument assesses overall health, pain and participation in normal daily activities.
Change from baseline in Mobility Scale of the Pediatric Evaluation of Disability Inventory
The Mobility Scale of the Pediatric Evaluation of Disability Inventory evaluates the child's functional mobility in everyday activities with regard to functional skills and caregiver assistance. The Paediatric Evaluation of Disability Inventory will be applied as a parental questionnaire, allowing comparison of the child's functional skills over time for each of the two dimensions.
Change from baseline in Pediatric Quality of Life Inventory Cerebral Palsy Module
The Pediatric Quality of Life Inventory Cerebral Palsy Module is a measure of health-related quality of life, specifically designed for children with CP. The Pediatric Quality of Life Inventory Cerebral Palsy Module is based upon the parents' report and measures physical, emotional, social and school functioning.
Change from baseline in Pediatric Outcome Data Collection Instrument
The Pediatric Outcome Data Collection Instrument assesses overall health, pain and participation in normal daily activities.

Full Information

First Posted
June 2, 2014
Last Updated
April 4, 2018
Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital, Sonderborg Hospital, Sygehus Lillebaelt, Hospital of South West Jutland, University of Salford, Region of Southern Denmark, Ludvig and Sara Elsass Foundation, Association of Danish Physiotherapists
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1. Study Identification

Unique Protocol Identification Number
NCT02160457
Brief Title
Gait Analysis and Interdisciplinary Interventions for Children With Cerebral Palsy
Acronym
CPinMotion
Official Title
Instrumented Gait Analysis and Individually Tailored Interdisciplinary Interventions for Children With Cerebral Palsy: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Completed
Study Start Date
August 6, 2014 (Actual)
Primary Completion Date
July 5, 2017 (Actual)
Study Completion Date
July 5, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital, Sonderborg Hospital, Sygehus Lillebaelt, Hospital of South West Jutland, University of Salford, Region of Southern Denmark, Ludvig and Sara Elsass Foundation, Association of Danish Physiotherapists

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to test the hypothesis, that improvements in gait pattern following individually tailored interventions guided by instrumented 3-dimensional gait analysis are superior to those used in 'care as usual'.
Detailed Description
Children with cerebral palsy (CP) who walk independently often have an altered gait pattern. Interdisciplinary interventions in terms of orthopaedic surgery, spasticity management, physical therapy and orthotics aim to improve the gait pattern. Standardised measurements are used in the Cerebral Palsy follow-Up Program to assess walking. However, these measurements do not describe features in the gait pattern reflecting underlying neuro-musculoskeletal impairments. This can be done with instrumented 3-dimensional gait analysis (IGA). It has never been investigated whether interdisciplinary interventions designed to address impairments identified by IGA result in improved gait pattern compared with 'care as usual' without IGA in children with CP. The aim of this study is to test the hypothesis, that improvements in gait pattern following individually tailored interventions guided by IGA are superior to those used in 'care as usual'. A prospective, single blind, randomised, parallel group study will be conducted. Participants will be recruited from the Cerebral Palsy follow-Up Program. Children aged 5 to 9 years with spastic CP, classified at Gross Motor Function Classification System levels I or II will be included. The interventions under investigation are 1) Individually tailored interdisciplinary intervention addressing impairments identified by IGA and 2) 'care as usual' (interdisciplinary interventions without IGA). The primary outcome is gait pattern measured by the Gait Deviation Index. Secondary outcome measures are, walking performance and patient-reported outcomes of functional mobility, health-related quality of life and overall health, pain and participation. Explorative outcome measures include walking performance, gait pattern, behavior of health care providers and the applied interventions. The primary endpoint for assessing the outcome of the two interventions will be 52 weeks after start of intervention. A follow up will also be performed at 26 weeks after start of intervention; however, exclusively for the patient-reported outcomes. To our knowledge, this is the first randomised controlled trial comparing the effects of an individually tailored interdisciplinary intervention designed to address impairments identified by IGA versus 'care as usual' in children with CP. Consequently, the study will provide novel evidence for the use of IGA in interdisciplinary interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Palsy
Keywords
Cerebral palsy, Instrumented gait analysis, Gait Deviation Index

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention with IGA
Arm Type
Experimental
Arm Description
Individually tailored interdisciplinary intervention based on measures performed as part of the Cerebral Palsy follow-Up Program and other clinical examinations AND instrumented gait analysis (IGA)
Arm Title
Intervention without IGA
Arm Type
No Intervention
Arm Description
'Care as usual' - Individually tailored interdisciplinary interventions based on measures performed as part of the Cerebral Palsy follow-Up Program and other clinical examinations BUT NOT (IGA).
Intervention Type
Other
Intervention Name(s)
Intervention with IGA
Other Intervention Name(s)
Vicon T40 system, Vicon, Oxford, UK, Advanced Mechanical Technology Inc. (AMTI), OR6-7-1000, Watertown, USA
Intervention Description
Individually tailored interdisciplinary intervention based on measures performed as part of the Cerebral Palsy follow-Up Program and other clinical examinations AND instrumented gait analysis The instrumented gait analysis consists of four steps: Instrumented gait analysis (data collection with a 8-camera Vicon T40 system (Vicon, Oxford, UK) and 2 force plates (AMTI, OR6-7-1000) Impairment-Focused Interpretation Recommendation for interdisciplinary interventions Dissemination of recommendations The two modalities differs in the use of IGA, but the study is not indented to document the effect of IGA alone, but to document the difference in the effects of the interdisciplinary interventions, when IGA is implemented to the experimental group.
Primary Outcome Measure Information:
Title
Change from baseline in Gait Deviation Index
Description
Gait Deviation Index (GDI) is based upon kinematic data from the Instrumented Gait Analysis, and is an quantitative index that summarises the overall gait pattern into a single score for each patient by comparison with non-pathological gait. A GDI value of 100 represents the absence of gait pathology, and each 10-point decrement below 100 indicates one standard deviation from normal gait kinematics. For the primary outcome measure, the median of five trials for each leg will be used to calculate the average of both legs to provide a single index for each child.
Time Frame
Baseline, 52 weeks
Secondary Outcome Measure Information:
Title
Change from baseline in 1-minute walk test
Description
Walking performance is assessed with the 1-minute walk test. The test measure the distance in meters, when the child walks as fast as possible.
Time Frame
Baseline, 52 weeks
Title
Change from baseline in Mobility Scale of the Pediatric Evaluation of Disability Inventory
Description
The Mobility Scale of the Pediatric Evaluation of Disability Inventory evaluates the child's functional mobility in everyday activities with regard to functional skills and caregiver assistance. The Paediatric Evaluation of Disability Inventory will be applied as a parental questionnaire, allowing comparison of the child's functional skills over time for each of the two dimensions.
Time Frame
Baseline, 52 weeks
Title
Change from baseline in Pediatric Quality of Life Inventory Cerebral Palsy Module
Description
The Pediatric Quality of Life Inventory Cerebral Palsy Module is a measure of health-related quality of life, specifically designed for children with CP. The Pediatric Quality of Life Inventory Cerebral Palsy Module is based upon the parents' report and measures physical, emotional, social and school functioning.
Time Frame
Baseline, 52 weeks
Title
Change from baseline in Pediatric Outcome Data Collection Instrument
Description
The Pediatric Outcome Data Collection Instrument assesses overall health, pain and participation in normal daily activities.
Time Frame
Baseline, 52 weeks
Title
Change from baseline in Mobility Scale of the Pediatric Evaluation of Disability Inventory
Description
The Mobility Scale of the Pediatric Evaluation of Disability Inventory evaluates the child's functional mobility in everyday activities with regard to functional skills and caregiver assistance. The Paediatric Evaluation of Disability Inventory will be applied as a parental questionnaire, allowing comparison of the child's functional skills over time for each of the two dimensions.
Time Frame
Baseline, 26 weeks
Title
Change from baseline in Pediatric Quality of Life Inventory Cerebral Palsy Module
Description
The Pediatric Quality of Life Inventory Cerebral Palsy Module is a measure of health-related quality of life, specifically designed for children with CP. The Pediatric Quality of Life Inventory Cerebral Palsy Module is based upon the parents' report and measures physical, emotional, social and school functioning.
Time Frame
Baseline, 26 weeks
Title
Change from baseline in Pediatric Outcome Data Collection Instrument
Description
The Pediatric Outcome Data Collection Instrument assesses overall health, pain and participation in normal daily activities.
Time Frame
Baseline, 26 weeks
Other Pre-specified Outcome Measures:
Title
Change from baseline in Gait Variable Score
Description
The Gait Variable Score is used to measure changes in gait pattern. Gait Variable Score is an index for a single gait variable. The Gait Variable Scores are determined for the following nine variables: Pelvic tilt, pelvic obliquity, pelvic rotation, hip flexion, hip adduction, hip rotation, knee flexion, dorsiflexion and foot progression
Time Frame
Baseline, 52 weeks
Title
Change from baseline in Measure of Processes of Care
Description
Measure of Processes of Care is a self-report measure of parents' perception of the extent to which the health services that their child receives are family-centred.
Time Frame
Baseline, 52 weeks
Title
Applied interventions
Description
Records from the Cerebral Palsy Follow-Up Program of the applied interventions will be used to explore differences (used vs. not used) in the use of the following intervention categories in the two groups: Orthopaedic surgery, Spasticity management, Physical Therapy and Orthotics.
Time Frame
52 weeks
Title
Difference in recommended and applied interventions
Description
Records from the Cerebral Palsy Follow-Up Program of the recommended and actually applied interventions in the experimental group will be used to explore the differences (used vs. not used) in the recommended and actually applied interventions in regard to the following categories: Orthopaedic surgery, Spasticity management, Physical Therapy and Orthotics.
Time Frame
Baseline, 52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Spastic Cerebral palsy Gross Motor Function Classification System levels I or II. Exclusion Criteria: Earlier interventions in the form of orthopaedic surgery within the past 52 weeks, injection with botulinum toxin type A in the 12 weeks prior to baseline assessments Relocation to another region during the trial. If the child not are able to demonstrate sufficient co-operation and cognitive understanding to participate in the IGA.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Helle Rasmussen, Ph.d. stud.
Organizational Affiliation
University of Southern Denmark and Odense University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anders Holsgaard-Larsen, Ph.d.
Organizational Affiliation
University of Southern Denmark and Odense University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
University of Southern Denmark - Odense University Hospital
City
Odense
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
32873289
Citation
Fonvig CE, Rasmussen HM, Overgaard S, Holsgaard-Larsen A. Effectiveness of instrumented gait analysis in interdisciplinary interventions on parents' perception of family-centered service and on gross motor function in children with cerebral palsy: a randomized controlled trial. BMC Pediatr. 2020 Sep 1;20(1):411. doi: 10.1186/s12887-020-02315-2.
Results Reference
derived
PubMed Identifier
26643822
Citation
Rasmussen HM, Pedersen NW, Overgaard S, Hansen LK, Dunkhase-Heinl U, Petkov Y, Engell V, Baker R, Holsgaard-Larsen A. The use of instrumented gait analysis for individually tailored interdisciplinary interventions in children with cerebral palsy: a randomised controlled trial protocol. BMC Pediatr. 2015 Dec 7;15:202. doi: 10.1186/s12887-015-0520-7.
Results Reference
derived

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Gait Analysis and Interdisciplinary Interventions for Children With Cerebral Palsy

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