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Acceptability and Feasibility of a New Postural Management Night-time Intervention to Improve Respiratory Health of Children With Complex Neuro-disability (Breathe-Easy)

Primary Purpose

Respiratory Aspiration

Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Novel Postural Management Night-time Intervention
Sponsored by
Sussex Community NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Respiratory Aspiration

Eligibility Criteria

2 Years - 19 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: dependent upon others to position/move their bodies high risk of aspiration linked to swallowing difficulties aged 2-18yrs have gastrostomy/jejunostomy receiving care from Consultant Respiratory Paediatrician from Royal Alexandra Children's Hospital (Dr Kapur or colleague) because of recent history of chest infections. Exclusion Criteria: Children with complex neuro-disability who cannot be positioned in such a way that promotes upper airway drainage Children using a naso-gastric tube Children who do not have a gastrostomy or jejunostomy

Sites / Locations

  • Chailey Clinical Services

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Novel Postural Management Night-time Intervention Components

Arm Description

Intervention Arm

Outcomes

Primary Outcome Measures

Liverpool Respiratory Symptom Questionnaire
Questionnaire Outcome Measure

Secondary Outcome Measures

Full Information

First Posted
September 8, 2023
Last Updated
September 8, 2023
Sponsor
Sussex Community NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT06039852
Brief Title
Acceptability and Feasibility of a New Postural Management Night-time Intervention to Improve Respiratory Health of Children With Complex Neuro-disability
Acronym
Breathe-Easy
Official Title
Breathe-Easy: a Pilot Study to Examine the Acceptability and Feasibility of a Novel Postural Management Night-time Intervention to Improve Respiratory Health of Children With Complex Neuro-disability.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 1, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sussex Community NHS Foundation Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This research concerns children with complex neuro-disability. Damage to the developing brain leads to lifelong disturbances in motor control, seizures, cognition, communication, eating and drinking, and behaviour. Children with complex neuro-disability are dependent upon others to move and position them. Children commonly experience chronic lung disease, leading to frequent hospitalisation, medical interventions and premature death. Respiratory illness may be triggered by "aspiration", i.e. when saliva, food, liquid or stomach contents enter the lungs. Aspiration risks increase at night-time when supervision is limited and children are positioned on their backs. Some children experience repeated breathing complications requiring prolonged hospital stays including respiratory support in intensive care. Consultant Respiratory Paediatrician Akshat Kapur and Physiotherapist Hilda Perry developed a new night-time intervention to improve respiratory health of children with complex neuro-disability. Dr Kapur and his team have found that this intervention can help reduce respiratory illness and time spent in hospital for some children. This is an acceptability and feasibility study which means we want to find out if this new intervention is something that children with complex neuro-disability and their families are happy (i.e. it is acceptable) and able (i.e. it is feasible) to do. If so, a larger future research study can be designed to find out if the intervention works to improve the respiratory health of children with complex neuro-disability.
Detailed Description
The intervention involves positioning children safely on their fronts using pillows to support the body under the shoulder and hip, and with the head slightly lowered so that gravity can help drain secretions from the mouth. This is different to current night-time positioning recommendations of either lying children on their backs or side. The new intervention also involves, where possible, the draining of children's stomach contents overnight via an existing feeding tube to prevent aspiration of stomach contents. We will work closely with 10 children with complex neuro-disability and their families, and health professionals as we introduce this new night-time intervention. We will make observations about children's respiratory and sleep outcomes before and after making changes. We will make comparisons using questionnaires, sleep diaries, records of antibiotic use and hospital admissions. We will collect this information before making any changes, at 3 months after the intervention has been established and after 6 months when the study ends. We will talk to children, parents, carers and relevant health professionals to find out what they think and feel about the new intervention, including any issues/challenges that occurred. We will record how many children and families were approached to take part in the study. We will record how many agreed to take part, how many chose to leave half way through and how many said they did not want to take part in the study. Families who discontinued or who declined the intervention will be given opportunity to provide feedback confidentially. We will use the findings to decide whether it is feasible and acceptable to children and families to run a research trial of this new night-time intervention. The data will help us to design a future research trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Aspiration

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Novel Postural Management Night-time Intervention Components
Arm Type
Experimental
Arm Description
Intervention Arm
Intervention Type
Other
Intervention Name(s)
Novel Postural Management Night-time Intervention
Intervention Description
Essential elements and components of PMN-TI: Safe and comfortable position to enable sleep Positioning to enable UAD overnight Quiet breathing unobstructed by base of tongue (i.e. stertor), vocal cords (i.e. stridor) or pooled secretions Postural support in lying to achieve comfort, promote symmetry of posture and maximum loadbearing Stomach contents reduced or emptied overnight to minimize reflux and associated aspiration risk.
Primary Outcome Measure Information:
Title
Liverpool Respiratory Symptom Questionnaire
Description
Questionnaire Outcome Measure
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: dependent upon others to position/move their bodies high risk of aspiration linked to swallowing difficulties aged 2-18yrs have gastrostomy/jejunostomy receiving care from Consultant Respiratory Paediatrician from Royal Alexandra Children's Hospital (Dr Kapur or colleague) because of recent history of chest infections. Exclusion Criteria: Children with complex neuro-disability who cannot be positioned in such a way that promotes upper airway drainage Children using a naso-gastric tube Children who do not have a gastrostomy or jejunostomy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah Crombie, PhD
Organizational Affiliation
Sussex Community NHS FT
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chailey Clinical Services
City
Brighton
State/Province
East Sussex
ZIP/Postal Code
BN8 4JN
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Acceptability and Feasibility of a New Postural Management Night-time Intervention to Improve Respiratory Health of Children With Complex Neuro-disability

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