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Physiotherapy for Children With Dysfunctional Breathing

Feasibility Study for a Multi-centre Trial Investigating Whether Physiotherapy Improves Outcomes for Children With Dysfunctional Breathing

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04215341
Acronym
PhysDB
Enrollment
31
Registered
2020-01-02
Start date
2014-08-04
Completion date
2016-08-08
Last updated
2020-01-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dysfunctional Breathing

Brief summary

Dysfunctional breathing in children primarily affects the ability to participate in sport or exercise but can also stop children doing other activities such as playing musical instruments. Clinical experience has shown that physiotherapy (through the use of breathing retraining and other associated techniques) can stop the symptoms of dysfunctional breathing, allowing children to return to normal activities and reduce or stop inhaled medications. Whilst there is some evidence in adults with this condition to support the use of physiotherapy, there have been no studies carried out in children investigating whether physiotherapy is beneficial for children with dysfunctional breathing. This study therefore aims to investigate the feasibility of a future large scale multicentre clinical trial designed to investigate whether physiotherapy improves outcomes for children with dysfunctional breathing. The improved management of this common but under recognised condition would lead to significant improvements in the quality of life of children coupled with the reduction in potentially harmful medications.

Interventions

BEHAVIORALPhysiotherapy

A course of breathing retraining delivered by a physiotherapist and practiced by the participant at home.

Sponsors

University of Sheffield
CollaboratorOTHER
Sheffield Children's NHS Foundation Trust
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 16 Years
Healthy volunteers
No

Inclusion criteria

Aged 8-16 years Clinical diagnosis of dysfunctional breathing

Exclusion criteria

Uncontrolled comorbidities Participant and parents/guardians not fluent in written and spoken English Inability to follow instructions

Design outcomes

Primary

MeasureTime frameDescription
Child and parent proxy report versions of the quality of life questionnaire(PedsQL)24 monthsTo measure participant and parent proxy report of quality of life in the four domains of physical, emotional, social and school functioning

Secondary

MeasureTime frameDescription
Symptom questionnaire (Nijmegen questionnaire)24 monthsTo measure the type and frequency of symptoms commonly associated with dysfunctional breathing
Structured light plethysmography (SLP) scan (Thora-3DI)24 monthsTo objectively measure breathing pattern and rate without influencing these parameters
Reliever inhaler usage recorded using a data logger device24 monthsTo measure usage of inhaled reliever medication

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 31, 2026