Epidemiology of Sleep Disordered Breathing in Children and Young People With Cerebral Palsy
NCT ID: NCT06737302
Last Updated: 2026-01-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
50 participants
OBSERVATIONAL
2025-03-01
2026-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Children with CP have a higher risk of sleep breathing problems compared to typically-developing children, and the negative impact of sleep disturbance in children with CP on their family members/carers' sleep and mental health cannot be understated. Early recognition and management of SDB is important for children with CP to give these children the best possible sleep quality, and to maximise learning potential.
SDB in children with CP is often under-recognised and under-treated. Treatment of SDB in children with CP might involve wearing a mask that delivers pressurised air to hold open a child's airway and make breathing easier when they are asleep. This is called 'respiratory support' which can be continuous pressure (CPAP) or non-invasive ventilation (NIV) which is pressure support with a back-up breathing rate. There is limited knowledge on the appropriate indications or timing to use them.
Though respiratory support in children with CP is proven to help with breathing during sleep, its impact on quality of life, number of hospital admissions or frequency of chest infections is unknown.
This study will look at the number of children with CP on respiratory support across the UK, as well as the number of children newly diagnosed with SDB and/or established on respiratory support over a 1-year period. This study will also explore socioeconomic factors that might influence access of sleep services and the perceived facilitators and barriers to successfully initiating respiratory support in children with CP.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Experiences of Managing Sleep Disordered Breathing in Children With Cerebral Palsy.
NCT06753370
Sleep-Disordered Breathing in Children With Cerebral Palsy at Increased Risk of Respiratory Disorders
NCT07077226
Risk Factors , Types and Neuroimaging Findings in Patients With Cerebral Palsy at Assiut University Children's Hospital
NCT06928012
Neuroradiology Assesses Chiari Malformation's Impact on Airways, Cranial Base, and Sleep Disorders in Children.
NCT05913297
Sleep-disordered Breathing in Infants With Myelomeningocele
NCT04251806
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
There is no national registry of children with cerebral palsy (CP) which collects information on sleep or sleep disordered breathing (SDB) for the purpose of this study. Hence, the investigators will recruit all tertiary paediatric centres across the UK which offers sleep services to children. A single point of contact will be identified for further communication and to act as local champion for collecting the relevant information in each centre.
I) National point prevalence survey;
* Single point of contact (PoCo) identified across tertiary paediatric centre which offer sleep services
* Single questionnaire sent on pre-specified date to PoCo in each centre
* Study will aim to;
* assess number of children in each centre with CP established on respiratory support
* gather information on practices in different centres pertaining to their assessment and management of children with CP and suspected SDB
II) National Incidence self reporting form;
* This phase of the review will a conducted over a 1-year period
* Will be conducted as a 2-part survey, with the PoCo being sent a monthly self-reporting form;
* Part A;
* To identify number of children with CP who underwent sleep study, the proportion of those who were diagnosed with SDB, and the total number of children with CP who were initiated on respiratory support (regardless of sleep study results) in that calendar month
* To be completed by PoCo in all centres
* If any children with CP were newly initiated on respiratory support (regardless of sleep study results), PoCo will be directed to complete Part B
* Part B;
* Will gather further information on children with CP who were initiated on respiratory support in the calendar month (regardless of sleep study results), with a separate form for each child
* Data collected will assess association between socio-economic factors (ethnicity, social deprivation index and urban-rural classification) and diagnosis of sleep disordered breathing and/or being initiated on respiratory support in children with CP
* No power calculation has been done for this review, as this is an observational study with an aim to include all children with cerebral palsy, newly diagnosed with SDB and/or started on respiratory support in the UK
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Any child aged ≤16 years old, with a confirmed diagnosis of cerebral palsy
* On respiratory support on the date of prevalence survey
Cases for Incidence self-reporting form;
* Part A;
* Any Child aged ≤16 years old, with confirmed diagnosis of cerebral palsy
* Had sleep studies for suspected sleep disordered breathing within the preceding calendar month
* Part B;
* Any Child aged ≤16 years old, with a confirmed diagnosis of cerebral palsy
* Initiated respiratory support (CPAP or NIV or invasive tracheostomy ventilation) in the preceding month
Exclusion Criteria
* Patient does not have a confirmed diagnosis of cerebral palsy
1 Month
16 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Edinburgh
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
NHS Lothian
Edinburgh, Edinbrugh, United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
AC24189
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.