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| ID | Type | Description | Link |
|---|---|---|---|
| 1R21AG086817-01A1 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Aging (NIA) | NIH |
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Poor sleep is common among Asian Americans. Untreated sleep problems increase the risk of chronic diseases, cognitive decline, and mortality. Cognitive behavioral therapy for insomnia (CBTI) is considered the first-line treatment for chronic sleep problems and has demonstrated significant improvement in sleep health among older adults. However, existing CBTI is built upon Western culture, making it challenging to apply for Asian immigrants who maintain close ties to their native cultures that shape and influence their sleep habits. Addressing the lack of availability of a culturally adapted sleep intervention program is the first step to filling the gap in sleep health disparity among Asian immigrants.
This study aims to pilot test the feasibility and the preliminary efficacy of a culturally adapted sleep intervention program among older Korean immigrants with poor sleep, one of the fastest-growing immigrant groups in the United States with limited access to mainstream sleep therapies.
Poor sleep is common among Asian Americans. Untreated sleep problems increase the risk of chronic diseases, cognitive decline, and mortality. Addressing the lack of availability of a culturally adapted sleep intervention program is the first step to filling the gap in sleep health disparity among Asian immigrants. This study aims to evaluate its feasibility and preliminary efficacy of a culturally adapted sleep education program ("SLEEP-OK") in a pilot randomized clinical trial. Study participant (N=32) will be randomized to either our culturally adapted, manual-based sleep intervention group (n=16) or the information-only control group (n=16) at our community partner serving older Korean immigrants. The study will evaluate the feasibility of the intervention and the preliminary effects of the intervention on sleep health outcomes among Korean immigrants at baseline and post-intervention (i.e., immediately after the last session of the intervention).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Sleep Intervention Program | Experimental | This is a culturally adapted sleep education program built upon key components of cognitive behavioral therapy for insomnia (CBT-I) |
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| Control | Placebo Comparator | This involves with general information about sleep |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CBT-I based sleep intervention | Behavioral | A multicomponent behavioral sleep program, consisting of sleep compression, stimulus control, sleep hygiene, relaxation, daily physical activity, and light exposure |
| Measure | Description | Time Frame |
|---|---|---|
| Objective Sleep Efficiency | Nighttime sleep efficiency (i.e., mean percent of time in bed spent asleep at nighttime) will be calculated from 7 consecutive days and nights of wrist actigraphy (Scores range from 0 to 100%, with higher values indicating better objective sleep quality) | Immediately after the last session of the intervention |
| Subjective Sleep Quality | Total score on the Korean version of the Insomnia Severity Index (ISI) will be used as a measure of subjective sleep (Scores range from o to 18, with lower values indicating better subjective sleep quality) | Immediately after the last session of the intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Acceptability of the Intervention | Focus group interviews will be conducted to collect the benefits and challenges of following the sleep intervention program | Immediately after the last session of the intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Feasibility of Recruitment | The number of participants approached who agreed to participate will be measured | Immediately after enrolled |
| Feasibility of Randomization and Retention | The number of participants lost at a post-treatment assessment will be measured |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Yeonsu Song, PhD | Contact | 310-983-3029 | ysong@sonnet.ucla.edu |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of California Los Angeles | Recruiting | Los Angeles | California | 90095 | United States |
IPD difficulty masking the identity of participants will not be shared publicly. However, all de-identified data and metadata will be made available through National Sleep Research Resource (NSRR), an NHLBI-funded resource at the time of the associated publication or the end of this project year, whichever comes first. Final research data and metadata will be shared by the end of the project period or at the time of publication, whichever is sooner, and will remain accessible indefinitely.
by the end of the project period or at the time of publication, whichever is sooner,
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| ID | Term |
|---|---|
| D007319 | Sleep Initiation and Maintenance Disorders |
| ID | Term |
|---|---|
| D020919 | Sleep Disorders, Intrinsic |
| D020920 | Dyssomnias |
| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |
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| Sleep Education | Behavioral | This group will receive information about sleep and aging, but without specific or individualized recommendations |
|
| Immediately after enrolled |
| Adherence to the Intervention | The total number of sessions and the percentage of days that participants met goals for recommendations throughout the intervention program will be measured | Immediately after the last session of the intervention |
| Interventionist Adherence | The percentage of completion of delivery of each component in sessions throughout the intervention program will be measured | Immediately after the last session of the intervention |
| D001523 |
| Mental Disorders |