- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01301989
Reducing Sleep Disparities in Minority Children
Reducing Sleep Disparities in Urban, Minority School-Aged Children
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Inclusion Criteria. Eligible families must: (1) have a typically developing healthy child age 5-6 years old enrolled in school for a minimum of 5 hours per day; (2) have a child who screens positive for a sleep problem based on the CSHQ (a score >41); (3) have lived in permanent housing within the catchment communities for the study (not in a shelter or other temporary housing) for the previous 12 months; (4) have no plans to move out of the area in the next 12 months; (5) agree to have research staff come into their homes for a home assessment and actigraph fitting every 3 months for 1 year; (6) have telephone access or a contact with telephone access; and (7) be fluent in either English or Spanish.
Exclusion criteria will include the presence of a serious co-morbid condition in the child that may impact sleep including: genetic syndromes, neuromuscular disorders, seizure disorder, mental retardation, autism, severe learning disabilities, psychiatric disorders, and attention-deficit/hyperactivity disorder. The presence of such co-morbid conditions would confound the outcome of interest.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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New York
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New York, New York, United States, 10032
- Columbia University Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy child age 5-6 years old
- School enrollment for a minimum of 5 hours/day
- Positive Children's Sleep Habits Questionnaire (score ≥ 41)
- Permanent housing for the previous 12 months
- Permission for research staff to complete 5-9 home over 1 year
- Have telephone access or a contact with telephone access
- Fluent in either English or Spanish
Exclusion Criteria:
Serious co-morbid condition that may impact sleep including:
- genetic syndromes
- neuromuscular disorders
- seizure disorder
- mental retardation
- autism
- severe learning disabilities
- psychiatric disorders
- attention-deficit/hyperactivity disorder
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Placebo Comparator: Sleep Education Control
The control group receives a low intensity intervention that provides information about sleep and the benefits of adequate sleep.
We will give parents the National Sleep Foundation's handout, "Information about Children's Sleep for Parents and Teachers" (in English and Spanish).
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The control group will receive a low intensity intervention that provides information about sleep and the benefits of adequate sleep.
We will give parents the National Sleep Foundation's handout, "Information about Children's Sleep for Parents and Teachers"
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|
Experimental: Sleep Counselor Intervention
The sleep counselor visits are to assess the family's understanding of their child's sleep problems; help parents recognize the child's sleep deficiency; discuss how sleep problems affect behavior, learning, and health; and reassure parents that the sleep counselor can help them with these problems. Additionally, sleep counselors: review parent's sleep goals to monitor changes to the child's bedtime routine and sleep environment; help them solve problems with implementation; provide positive feedback to help the parent recognize success; and help parents set additional goals for improving sleep. |
Families in the sleep counselor arm of the study will receive 3 scheduled home visits by a trained sleep counselor during the first 3 months following enrollment.
Two optional home visits may be scheduled to help families encountering ongoing barriers to improving their child's sleep.
The intervention will be provided by trained, bilingual, culturally competent sleep counselors, who will assess home sleep conditions, work with the family to teach them how to improve sleep hygiene and the sleep environment, provide equipment as needed to improve the sleep environment (e.g.
nightlight, inflatable bed, window shade, etc.) and guide the family to begin setting goals and making decisions to initiate and sustain behavioral and environmental changes to improve sleep.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sleep Duration
Time Frame: Baseline and 3 month intervals for 12 months
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The primary outcome is nightly sleep duration and is objectively measured using actigraphy.
The actigraph is worn on the non-dominant wrist for 7 consecutive days and nights.
Actigraphy is a well-validated method for evaluating sleep and circadian rhythm patterns in children.
It is highly correlated with polysomnography.
To reduce potential confounders, Actiwatches are worn 5 times during the study, at baseline and at 3, 6, 9, 12 months following collection of baseline data.
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Baseline and 3 month intervals for 12 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sleep Fragmentation
Time Frame: Baseline, 3, 6, 9, and 12 months
|
Sleep fragmentation (average number and duration of nightly awakenings in each 7-day period) measured by actigraphy and parental sleep logs.
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Baseline, 3, 6, 9, and 12 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Beverley J Sheares, MD, MS, Columbia University
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- AAAE4951
- R01HL092856 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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