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Clinical Trials/NCT04728191
NCT04728191
Recruiting
Not Applicable

The Effect of Physiotherapy on Dysfunctional Breathing in Children and Adolescents With and Without Asthma.

Kolding Sygehus1 site in 1 country140 target enrollmentFebruary 10, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dysfunctional Breathing
Sponsor
Kolding Sygehus
Enrollment
140
Locations
1
Primary Endpoint
Change from baseline in Pediatric Quality of Life Inventory ( PedsQl) at 6 months
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The purpose of the study is to investigate the effect of physiotherapeutical instructions on dysfunctional breathing in children and adolescents with or without asthma.

Children and adolescents with dysfunctional breathing, are invited to participate in the intervention study. Participants are stratified by asthma diagnose status and randomized to physiotherapy or standard care. Participants are followed a year after the intervention, to compare the development in asthma control ( if asthma) and quality of life.

Detailed Description

The purpose of the study is to investigate the effect of physiotherapeutical instructions on dysfunctional breathing in children and adolescents with or without asthma. All children and adolescents aged 10-17 years, followed in our outpatient clinic with the diagnose of asthma are invited to fulfill the Nijmegen Questionnaire (NQ) and the Asthma Control Questionnaire (ACQ5) Children and adolescents where asthma was investigated and ruled out are invited to fulfill the NQ. Data from the electronic patient journal are used as descriptives. Participants with dysfunctional breathing (NQ \>= 23) are invited to participate in the intervention study. Participants are stratified by asthma diagnose status and randomized to physiotherapy or standard care. Participants are followed a year after the intervention, to compare the development in asthma control measured by ACQ5 (if asthma) and quality of life measured by PedsQL. The effect of physiotherapy is analyzed separately for participants with and without asthma. In addition, primary outcomes are analyzed in a regression model with asthma status, age and sex as explanatory variables.

Registry
clinicaltrials.gov
Start Date
February 10, 2021
End Date
December 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Kolding Sygehus
Responsible Party
Principal Investigator
Principal Investigator

Signe Vahlkvist

Principal Investigator

Kolding Sygehus

Eligibility Criteria

Inclusion Criteria

  • Asthma group:
  • Asthma diagnosed by lung function tests and/or typical symptoms.
  • Treatment with inhaled corticosteroids in minimum 3 months.
  • ACQ5 \>= 1.
  • NonAsthma group
  • Asthma denied after lung function tests ( exercise challenge or mannitol challenge)
  • NQ \>= 23.

Exclusion Criteria

  • Other significant cardiopulmonary or muscoluskeletal conditions.
  • Complex functional conditions involving other organ systems.
  • patients who already had the physotherapeutical intervention before study start.

Outcomes

Primary Outcomes

Change from baseline in Pediatric Quality of Life Inventory ( PedsQl) at 6 months

Time Frame: PedsQL is taken at baseline and 6 months after intervention as primary outcome.

PedsQl consists of 23 questions in 4 segments ( physical functioning, emotions, social interaction, and school activities). Each question is scored from 0 (best) to 4 (worst). The PedsQl questionnairre exists in formats for young children ( not used here), children aged 8-12 years and Teenagers aged 13-18 years. Children and adolescents are answering the age relevant questionnairre at visits in the out patient clinic. The PedsQl score is transformed to a 0-100 scale as follows: 0 =100, 1=75, 2=50, 3=25, 4=0. Health related Quality of life is calculated as a mean of scores. Psychosocial Health summary score is calculated as a mean of scores in the emotional, social and school functioning scales. Physical Health summary score is calculated as physical functioning scale score mean.

Change from baseline in Asthma Control Questionnaire ( ACQ5) at 6 months.

Time Frame: ACQ is taken at baseline and 6 months after intervention as primary outcome.

ACQ5 contains 5 questions regarding asthma symptoms. Each question is scored between 0-6 points, where 0 represents very good asthma control and 6 represents poor asthma control. Total ACQ score is calculates as an average of points. ACQ5 is taken by participants with asthma, at visits in the outpatient clinic.

Secondary Outcomes

  • Change from baseline in Pediatric Quality of Life Inventory ( PedsQl) at at 6 weeks and one year. Change from 6 months in PedsQl at 12 months.(PedsQl is taken at 6 weeks and 12 months after intervention as secondary outcomes.)
  • The reported use of rescue Beta2 agonist in puffs per week(at baseline and 6 weeks, 6 months and 12 months after intervention.)
  • Change from baseline in Brompton breathing Pattern Assesment Tool ( BBPAT)(BBPAT is taken at baseline and 6 weeks, 6 months and 12 months after intervention.)
  • Number of contacts to the hospital during one year from baseline(from baseline to 12 months after intervention.)
  • Change from baseline in Asthma Control Questionnaire ( ACQ5) at 6 weeks and one year. Change from 6 months in ACQ at 12 months.(ACQ5 is taken at 6 weeks and 12 months after intervention as secondary outcomes.)
  • Change from baseline in Nijmegen Questionnaire ( NQ)(NQ is taken at baseline and 6 weeks, 6 months and 12 months after intervention.)

Study Sites (1)

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