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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04539990
Other study ID # sor 0266-20 ctil
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 2020
Est. completion date September 2023

Study information

Verified date August 2020
Source Soroka University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The present study will test the effectiveness of a behavioral intervention program that targets sleep problems in 1.5-5-year-old children with ASD. Sleep patterns will be measured using questionnaires and sleep diaries that will be completed by the parents as well as by Fitbit sensors that will be placed on the child's wrist or back of the arm. The study will also explore whether specific child (e.g., severity of cognitive abilities) or parent characteristics (e.g., parent stress levels) impact the effectiveness of the intervention. In addition, we will examine whether changes in sleep disturbances are associated with changes in the family's quality of life.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date September 2023
Est. primary completion date September 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Months to 5 Years
Eligibility Inclusion Criteria:

Parents of 1.5-5-year-old children with autism will be asked to fill the Child Sleep Habits Questionnaire (CSHQ). Those who report high scores on the following 3 CSHQ subscales will be invited to participate: bedtime resistance, sleep onset delay, and night-wakings.

Exclusion Criteria:

None

Study Design


Intervention

Behavioral:
Behavioral treatment for sleep difficulties
This intervention is mediated by the parents. Parents are educated regarding sleep hygiene and instructed to follow simple rules which create a reliable evening routine and reduce exposure to stimulating factors that delay sleep onset (e.g., caffeine or exercise). In addition, parents are asked to initiate a "fading" behavioral protocol whereby they teach their child to fall asleep independently, with less parental attention. This requires parents to limit their interaction with their child after the children are put to bed so as not to interfere with sleep onset. This includes limiting conversations and lying in bed with the child. This behavioral approach is applied gradually and is expected to reduce the time it takes children to fall asleep.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Soroka University Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary Child Sleep Habits Questionnaire Parent questionnaire regarding sleep habits of their child 8 weeks after program begins
Primary Night time sleep as measured by Fitbit sensor Sensor is placed on the arm of the child for 5 days and measures sleep 8 weeks after program begins
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