Physical Activity Clinical Trial
Official title:
Examining the Association Between Physical Activity and Sleep Quality in Children With Autism Spectrum Disorder Using Melatonin-mediated Mechanism Model: A Randomized Controlled Trial
This study aims to investigate whether physical activity intervention would be effective to improve sleep quality in children with ASD, and investigate how physical activity impacts on sleep in children with ASD through melatonin-mediated mechanism model. A parallel-group randomized controlled trial comparing a 12-week jogging intervention and a control group receiving standard care in 32 children with ASD will be conducted. This study will monitor the changes of four sleep parameters (sleep onset latency; sleep efficiency, wake after sleep onset and sleep duration) through objective actigraphic assessment and parental sleep logs.
Status | Not yet recruiting |
Enrollment | 32 |
Est. completion date | June 2019 |
Est. primary completion date | June 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 9 Years to 12 Years |
Eligibility |
Inclusion Criteria: - pre-puberty or early puberty as indicated by Tanner stage I or II ; - ASD diagnosis from a physician based on Diagnostic and Statistical Manual of Mental Disorders, 5th edition, (DSM-V)[42] - non-verbal IQ over 40 - the ability to follow instructions; - physically able to participate in the intervention - no additional regular participation in physical exercise other than school physical education classes for at least 6 months prior to the study - no concurrent medication for at least 6 months before the study or any prior melatonin treatment; - have sleep difficulties, including sleep onset insomnia and frequent and prolonged nightwaking and/or early morning awakenings reported by parents Exclusion Criteria: - with one or co-morbid psychiatric disorders as established by a structured interview based on DSM-V - with other medical conditions that limit their physical activity capacities (e.g., asthma, seizure, cardiac disease); - with a complex neurologic disorder (e.g., epilepsy, phenylketonuria, fragile X syndrome, tuberous sclerosis) |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
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The Hong Kong Polytechnic University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Sleep onset latency | Sleep onset latency (length of time taken to fall asleep, expressed in minutes, SOL) will be objectively measured by a GT3X accelerometer. | 12-week | |
Primary | Sleep efficiency | Sleep efficiency (actual sleep time divided by time in bed, expressed as a percent, SE) will be objectively measured by a GT3X accelerometer. | 12-week | |
Primary | Wake after sleep onset | Wake after sleep onset (length of time they were awake after sleep onset, expressed in minutes, WASO) will be objectively measured by a GT3X accelerometer. | 12-week | |
Primary | Sleep duration | sleep duration (total sleep in hours and minutes, SD) will be objectively measured by a GT3X accelerometer. | 12-week | |
Primary | Parental-assessed sleep quality | Participants' sleep patterns will be logged by their parents using Children's Sleep Habits Questionnaire (CSHQ), which is a validated 45-item parent-administered questionnaire to examine sleep patterns of young children. The total score ranged from 45 to 135. | 12-week | |
Primary | Melatonin | All participants will be instructed to collect a 24-h urine sample. 6-sulfatoxymelatonin, a creatinine-adjusted morning urinary melatonin and representative of melatonin level, will be measured from the sample. The weekend has been chosen to allow the participants to stay at home for sample collection. All urine samples will be collected using 24-h urine bottles containing 0.1L of 0.5M hydrochloric acid as a preservative. | 12-week |
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