Gait Analysis and Interdisciplinary Interventions for Children With Cerebral Palsy

NCT02160457 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2018-04-06

No results posted yet for this study

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'.

Conditions

  • Cerebral Palsy

Interventions

OTHER

Intervention with IGA

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: 1. Instrumented gait analysis (data collection with a 8-camera Vicon T40 system (Vicon, Oxford, UK) and 2 force plates (AMTI, OR6-7-1000) 2. Impairment-Focused Interpretation 3. Recommendation for interdisciplinary interventions 4. 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.

Sponsors & Collaborators

  • Odense University Hospital

    collaborator OTHER
  • Sonderborg Hospital

    collaborator OTHER_GOV
  • Sygehus Lillebaelt

    collaborator OTHER
  • Esbjerg Hospital - University Hospital of Southern Denmark

    collaborator OTHER
  • University of Salford

    collaborator OTHER
  • Region of Southern Denmark

    collaborator OTHER
  • Ludvig and Sara Elsass Foundation

    collaborator UNKNOWN
  • Association of Danish Physiotherapists

    collaborator OTHER
  • University of Southern Denmark

    lead OTHER

Principal Investigators

  • Helle Rasmussen, Ph.d. stud. · University of Southern Denmark and Odense University Hospital

  • Anders Holsgaard-Larsen, Ph.d. · University of Southern Denmark and Odense University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
5 Years
Max Age
8 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-08-06
Primary Completion
2017-07-05
Completion
2017-07-05

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02160457 on ClinicalTrials.gov