Sleep Support for Children With Neurodevelopmental Disorders

Sponsor
Sheffield Children's NHS Foundation Trust (Other)
Overall Status
Recruiting
CT.gov ID
NCT05971212
Collaborator
(none)
76
1
2
32
2.4

Study Details

Study Description

Brief Summary

Around 80% of children with neurodevelopmental disorders such as Attention Deficit Hyperactivity Disorder (ADHD) and autism are reported to have significant difficulties with sleep. This may be a problem with settling off to sleep, waking repeatedly in the night, or both.

Often these children will be prescribed a medication called melatonin to help them sleep, but there is no strong evidence of its effectiveness in children, the long-term side effects are not known and prescriptions for this drug cost millions of pounds a year for the NHS. Many children continue to have persistent sleep problems despite taking melatonin. Sleep support programmes delivered by nurses and sleep practitioners are known to be effective and to give parents and young people long-term strategies for promoting sleep without the use of medication. However, sleep support services are not universally funded.

In this feasibility study 76 children with ADHD, autism or other neurodevelopmental disorder who have been prescribed and have been regularly taking melatonin for at least a year but still have severe sleep difficulties will be recruited. The investigators will help to improve the child's sleep with a sleep practitioner support programme and, if possible, reduce the dose of melatonin or stop it completely if it is no longer needed. Using this design, it will be possible to test whether a programme delivered by sleep practitioners will significantly improve sleep for children using a non-medical approach and in turn improve the health and well-being of the child and family and reduce melatonin prescribing, thereby saving NHS resources and the potential for long-term side effects. The study design will be delivered by Sheffield Children's Hospital and supported by parent users, the Sleep Charity and Sheffield CCG. The results will be disseminated widely to local, regional and national groups as well as via social media.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Behavioural sleep clinic access
N/A

Detailed Description

Sleep is a restorative process, fundamental to physical and psychological health. Sleep disturbances including bedtime resistance and night-time awakening occur in 80% children with neurodisability, the most common associations being with Attention Deficit Hyperactivity Disorder (ADHD), Autism, cerebral palsy and syndromes such as Down, Prader-Willi and Angelman syndromes. In a meta-analysis of subjective and objective studies found that ADHD is associated with higher bedtime resistance, sleep-onset difficulty and longer latency, night awakenings, trouble waking up in the morning, sleep-disordered breathing, daytime sleepiness, more shifts between sleep stages, lower sleep efficiency and less sleep time. Anxiety and depression symptoms may have a significant role in the prevalence of sleep difficulties which would be clearly observed in bedtime resistance, sleep anxiety, night time awakenings and sleep onset delay. Thus, teaching children how to develop sleep hygiene and the use of behavioural modification to manage their fears would help children to fall asleep easily and reduce bedtime resistance which therefore would improve sleep quantity and quality.

The impact of sleep disturbance on children's health is wide-ranging with sleep deprivation leading to difficulties with mood, psychosocial problems and a detrimental impact on the child's cognitive ability and learning. Parents of children with sleep difficulties can suffer high levels of stress and anxiety, decreased ability to work or to drive safely, relationship and financial problems. These stresses lead to an increased demand on NHS primary care services and to prescriptions of drugs such as antidepressants. Children with significant sleep difficulties in the UK are often treated with melatonin, a hormone playing a key role in the timing of sleep-wake cycle, despite the findings of a recent systematic review that suggest that evidence does not strongly support its use. The drug is costly to the health service, with individual Clinical Commissioning Groups (CCGs) spending up to £500k per year on prescription charges for this drug alone.

Evidence from sleep clinics delivered in the local authority, NHS and voluntary sectors has shown that an intensive sleep support intervention can be highly effective. A recent retrospective evaluation of a nurse-led sleep support service successfully discharged 63% children without melatonin prescriptions after a median of two face-to face visits and three telephone calls. The proposed study will aim to support children with neurodevelopmental problems taking melatonin for sleep difficulties to develop long-term strategies for promoting sleep and to reduce drug prescriptions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
76 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Masking:
Single (Care Provider)
Primary Purpose:
Treatment
Official Title:
Can a Supportive Sleep-Practitioner-led Intervention Lead to Improved Sleep, Wellbeing and Reduced Medication Prescribing for Children With Neurodevelopmental Disorders and Co-occurring Severe Sleep Difficulties?
Actual Study Start Date :
Jan 29, 2021
Anticipated Primary Completion Date :
Sep 30, 2023
Anticipated Study Completion Date :
Sep 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Access to Sleep Clinic immediately

Behavioral: Behavioural sleep clinic access
Access to behavioural Sleep Clinic

Experimental: Control

Access to Sleep Clinic delayed

Behavioral: Behavioural sleep clinic access
Access to behavioural Sleep Clinic

Outcome Measures

Primary Outcome Measures

  1. Sleep Diary [20 weeks]

    7 day sleep diary (parent report)

  2. Actiwatch data [20 weeks]

    Actiwatch worn for a 7 day period

  3. Child Sleep Habits Questionnaire (CSHQ) [20 weeks]

    Child Sleep Habits Questionnaire (CSHQ)

  4. Melatonin Prescription Status [20 weeks]

    Questionnaire (designed by researchers) asking about patient dosage and type of melatonin taken

Secondary Outcome Measures

  1. Strengths and Difficulties Questionnaire (SDQ) [20 weeks]

    Strengths and Difficulties Questionnaire (SDQ)

  2. CHU-9D Quality of Life questionnaire [20 weeks]

    CHU-9D Quality of Life questionnaire

  3. Healthcare Utilisation [20 weeks]

    Questionnaire (designed by researchers) recording how many times patient has accessed healthcare settings/professionals in last year

  4. Parent Wellbeing [20 weeks]

    Warwick- Edinburgh Mental Wellbeing Scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 11 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children to be included will fulfil all of the inclusion criteria.

  • Formal diagnosis of ADHD, autism or another neurodevelopmental condition,

  • Age 4-11 years,

  • Severe sleep disturbance (defined as Score of 3 or more on Composite Sleep Disturbance Index),

  • Been taking melatonin to aid sleep onset for more than 12 months

Exclusion Criteria:
  • Exclusion Criteria

  • Already accessed a sleep clinic at Sheffield Children's Hospital or The Sleep Charity.

  • English not first language

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinical Research Facility, Sheffield Children's Hospital Sheffield United Kingdom

Sponsors and Collaborators

  • Sheffield Children's NHS Foundation Trust

Investigators

  • Study Director: Heather Elphick, Sheffield Children's NHS Trust

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sheffield Children's NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT05971212
Other Study ID Numbers:
  • SCH-2530
First Posted:
Aug 2, 2023
Last Update Posted:
Aug 2, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2023