Autism Spectrum Disorder Clinical Trial
Official title:
Pilot RCT to Compare a Home Based Tailored Cognitive Behavioral Therapy for Insomnia (CBT-I) Versus Webased CBT-I to Improve Sleep in Caregivers With Insomnia in the Context of Caring for a Child With Autism Spectrum Disorder
Autism Spectrum Disorder (ASD) represents one of the most perplexing neurobiological disorders with a prevalence of 1 in 54 children. The lifelong challenging and disruptive behaviors often associated with ASD requires caregivers to change their behavior and modify their environments to provide an ecosystem for optimal outcomes for their child, family and themselves. ASD behaviors can have significant impact on caregivers mental health and family functioning, including the ability to develop and maintain healthy sleep routines. The caregiving population in US has a high prevalence of insomnia; two thirds of caregivers experiencing difficulties falling and/or staying asleep. The prevalence of insomnia in children with ASD is equally high, 60-80% experiencing night waking contributing to poor daytime behavior and disrupted sleep in the caregivers. This pilot RCT will focus on improving caregivers sleep in the context of caring for a child with ASD and insomnia with a multi-disciplinary team. The investigators will compare a home-based tailored CBT for Insomnia (CBT-I) versus a web-based Way to Health CBT-I intervention. This data will support a larger RCT with the Department of Defense funding opportunity through the Congressionally Directed Medical Research Program. This Autism Research Program focuses on improving lives of those living with ASD.
Status | Recruiting |
Enrollment | 80 |
Est. completion date | November 15, 2024 |
Est. primary completion date | August 15, 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 3 Years to 100 Years |
Eligibility | Inclusion Criteria for Caregiver with a child with ASD: - Caregiver age 18 years or older - Diagnosis of Insomnia - Parental/guardian will give permission (informed consent) for child - Telephone and web Access - Stable medical and behavioral conditions, with no change in health status in the past three months - Commitment to maintaining stable medication doses and keeping medication consistent Inclusion Criteria for Children with ASD: - Children age 3 to 17 years and one of their parents - Diagnosis of Autism Spectrum Disorders, confirmed with Autism Diagnostic Observation Schedule and/or DSM-IV criteria. - Diagnosis of Behavioral Insomnia or Insomnia due to ASD (Insomnia due to internal - Parental/guardian permission (informed consent) and if appropriate, child assent. - Telephone and web Access - Stable medical and behavioral conditions, with no change in health status in the past - Commitment to maintaining stable medication doses and keeping child's sleep medication consistent Key exclusion criteria for Caregiver and child with ASD: - Insomnia due to co-occurring medical conditions and/ or sleep disorders such as obstructive sleep apnea (OSA), narcolepsy, restless leg syndrome, severe reflux, nocturnal asthma - Unstable co-occurring medical conditions such as epilepsy or other neurological disorders, sickle cell anemia, diabetes or severe eczema - Significant hearing or vision loss - Known genetic disorders such as Fragile X, 22ql 1.2 Deletion Syndrome, Rett Disorder, Down Syndrome. - Subjects who, in the opinion of the Investigator, may be nonĀ¬ compliant with study schedules or procedures. |
Country | Name | City | State |
---|---|---|---|
United States | University of Pennsylvania | Philadelphia | Pennsylvania |
United States | University of Pennsylvania | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pennsylvania | Children's Hospital of Philadelphia |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Caregiver Acceptability Opinion Survey | Opinion Survey with 8 items rated on a 7- point Likert scale. minimum of 0 and max of 56 with a score of 40 or greater will be considered acceptable for this study. | At week 8 | |
Primary | Feasibility of pilot study | This study will be considered feasible if we obtain a 70% completion rate for the all measures. | At week 8 | |
Secondary | Change in reported sleep on sleep diaries | Participants will be asked to record the amount of sleep each night | 8 weeks | |
Secondary | Change in Caregiver behaviors | Depression questionnaire: Patient Health Questionnaire -9 with a minimum score of 0 and max of 27 with lower scores representing better outcome | week 8 | |
Secondary | Change in Child Daytime behaviors | Child Behavior Checklist (CBCL) T scores of 0 to 100 with lower scores representing better outcome | week 8 | |
Secondary | Change in total sleep time average measured by an actigraphy watch for caregiver | Total sleep time in minutes on average for the week | week 8 | |
Secondary | Change in sleep latency as measured by actigraphy watch for caregiver | sleep latency in minutes on average for the week | week 8 | |
Secondary | Change in wake after sleep onset as measured by by actigraphy watch for caregiver | wake after sleep onset in minutes on average for the week | week 8 | |
Secondary | Change in total sleep time as measured by actigraphy watch for child | Total sleep time in minutes on average for the week | week 8 | |
Secondary | Change in sleep latency as measured by actigraphy watch for child | sleep latency in minutes on average for the week | week 8 | |
Secondary | Change in wake after sleep onset as measured by actigraphy for child | wake after sleep onset in minutes on average for the week | week 8 | |
Secondary | Change in Maternal Self-efficacy | Maternal-Self efficacy Scale, 10 items with minimum score of 10 and maximum of 40 with higher scores representing better outcome | week 8 |
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