Skip to main content
Clinical Trials/NCT03530982
NCT03530982
Unknown
Not Applicable

Intensive Training of Functional Priorities Reported by Adolescents With Cerebral Palsy

Federal University of Minas Gerais1 site in 1 country20 target enrollmentJune 2, 2018
ConditionsCerebral Palsy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Palsy
Sponsor
Federal University of Minas Gerais
Enrollment
20
Locations
1
Primary Endpoint
Change in Daily functioning- Mobility
Last Updated
7 years ago

Overview

Brief Summary

Adolescents with cerebral palsy (CP) present important limitations for the performance of daily living activities. The aims of the study is to evaluate the feasibility and effects of an intensive goal training protocol for adolescents with CP. He hypothesize that adolescents submitted to the studied protocol will present improvements in performance and satisfaction of prioritized functional goals.

Detailed Description

We will conduct a feasibility study to assess the implementation and the possible effects of an intensive individualized goal training with adolescents with CP. Adolescents will select up to 5 functional goals to be trained during a 2 weeks, 3 hour-daily training, totalling 30 hours across 2 weeks. Moreover, they will be asked to daily practice these activities at home along the intervention period.

Registry
clinicaltrials.gov
Start Date
June 2, 2018
End Date
June 30, 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Federal University of Minas Gerais
Responsible Party
Principal Investigator
Principal Investigator

MARINA B BRANDAO

Professor

Federal University of Minas Gerais

Eligibility Criteria

Inclusion Criteria

  • Medical diagnosis of bilateral CP;
  • Age between 12 and 17 years old;
  • Manual Ability Classification System (MACS) ranging from levels I to III;
  • Gross Motor Function Classification System (GMFCS) ranging from levels I to IV;
  • Ability to understand verbal instructions.

Exclusion Criteria

  • Botulinum toxin or surgery in upper limbs in the previous 6 months of the study.

Outcomes

Primary Outcomes

Change in Daily functioning- Mobility

Time Frame: 1 month before intervention; pre-intervention; immediate post-intervention, 3-month follow-up

Pediatric Evaluation Disability Inventory (PEDI) mobility: ranging from 0-55; higher values, better outcomes

Change in Daily functioning- Self-Care

Time Frame: 1 month before intervention; pre-intervention; immediate post-intervention, 3-month follow-up

Pediatric Evaluation Disability Inventory (PEDI) self-care: ranging from 0-63; higher values, better outcomes

Change in Functional Goals

Time Frame: 1 month before intervention; pre-intervention; immediate post-intervention, 3-month follow-up

Canadian Occupational Performance Measure (COPM) (ranging 1-10; higher values, better outcomes)

Secondary Outcomes

  • Change in Manual dexterity(1 month before intervention; pre-intervention; immediate post-intervention, 3-month follow-up)
  • Change in Gross motor function(1 month before intervention; pre-intervention; immediate post-intervention, 3-month follow-up)
  • Change in Participation at home(1 month before intervention; pre-intervention; immediate post-intervention, 3-month follow-up)
  • Change in Participation in household activities(1 month before intervention; pre-intervention; immediate post-intervention, 3-month follow-up)

Study Sites (1)

Loading locations...

Similar Trials