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Clinical Trials/NCT02523521
NCT02523521
Unknown
Not Applicable

Impacte d'un Programa d'Exercici Per Nens d'Entre 4 a 6 Anys Amb Displàsia Broncopulmonar

Hospital de Nens de Barcelona1 site in 1 country52 target enrollmentAugust 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bronchopulmonary Dysplasia
Sponsor
Hospital de Nens de Barcelona
Enrollment
52
Locations
1
Primary Endpoint
aerobic capacity measured by shuttle run test
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine the effects of a physical activity program for children with Bronchopulmonary Dysplasia.

Detailed Description

Primary objectives is: to compare exercise tolerance and aerobic capacity between healthy children with Bronchopulmonary Dysplasia children Only Bronchopulmonary Dysplasia children will realise the physical activity program. Secondary objectives are: to analyse lung function and to evaluate flexibility.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
November 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital de Nens de Barcelona
Responsible Party
Principal Investigator
Principal Investigator

Morales

physiotherapist

Hospital de Nens de Barcelona

Eligibility Criteria

Inclusion Criteria

  • age between 4 to 6 years old
  • Bronchopulmonary Dysplasia diagnostic
  • ex-prematurity
  • accept to participate.

Exclusion Criteria

  • congenital malformations
  • neuromuscular disorders
  • gait alterations
  • difficulties for communication and understanding
  • wheezing or pulmonary disease two weeks before to start the program
  • hemodynamic changes (heart rate \> 130bpm, systolic blood pressure \> 130bpm, diastolic blood pressure \> 80bpm).
  • heart and/or lung transplantation.
  • Healthy children Criteria:
  • Inclusion Criteria:
  • age between 4 to 6 years old.

Outcomes

Primary Outcomes

aerobic capacity measured by shuttle run test

Time Frame: 15 minutes

effort tolerance measured by six minute walking test

Time Frame: six minutes

Secondary Outcomes

  • lung function measured by spirometry(5 minutes)
  • flexibility measured by sit and reach test(2 minutes)

Study Sites (1)

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