Sleep
Conditions
Keywords
sleep regularity, brief behavioral intervention, young adults
Brief summary
This study will employ a randomized controlled trial design to investigate the effects of a brief behavioral intervention that includes (1) self-recording of a regularity-focused sleep diary, (2) 10 strategies for maintaining sleep regularity, and (3) a sleep education information sheet on the maintenance of sleep regularity in young adults during the Christmas break.
Interventions
BEHAVIORALBrief behavioural intervention
Participants will receive a brief behavioural intervention comprising a regularity-focused sleep diary, 10 tips for maintaining sleep regularity, and a sleep education information sheet. The regularity-focused sleep diary is designed to emphasize in-bed and out-of-bed times, drawing participants' attention to their sleep regularity. Participants will be provided with a yellow marker to highlight their sleep periods. The 10 tips for maintaining sleep regularity include establishing a consistent out-of-bed time, using natural light to regulate the circadian clock, adjusting mealtimes, etc. The sleep education sheet contains information on reducing caffeine intake in the afternoon, limiting screen time before bed, etc.
BEHAVIORALHealth education
Participants will receive general health information without specific emphasis on sleep, such as weight control, smoking cessation, etc.
Sponsors
The University of Hong Kong
Chinese University of Hong Kong
Hong Kong Baptist University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)
Masking description
Due to the nature of the intervention, participants cannot be blinded. However, they will be unaware of the true aim of the study and will be informed that the intervention is intended to enhance overall well-being. Outcome measures will be administered by research personnel who are blinded to group allocation.
Eligibility
Sex/Gender
ALL
Age
18 Years to 24 Years
Healthy volunteers
Yes
Inclusion criteria
1. Young adults aged 18-24 years; 2. Will stay in Hong Kong during the study period; 3. Will not engage in any activities that require a fixed sleep or wake-up time (e.g., work or study during the holiday period) as these activities could regularize the sleep schedule and potentially contaminate the results.
Exclusion criteria
1. Have been in a different time zone within two weeks before the baseline assessment; 2. Diagnosed with circadian rhythm disorders such as delayed sleep-wake phase disorder (DSWD), advanced sleep-wake phase disorder (ASWD), irregular sleep-wake rhythm disorder (ISWRD), and non-24-hour sleep-wake rhythm disorder (N24WSD); 3. Diagnosed with sleep disorders that directly/indirectly interfere with sleep regularity (e.g., insomnia, sleep apnea); 4. Use of medications or treatment that may influence sleep regularity (e.g., hypnotics, antidepressants); 5. Diagnosed with serious physical or mental diseases such as cancer, end-stage liver or kidney diseases, schizophrenia, and psychosis.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Sleep regularity | From baseline assessment to the end of intervention at 3 weeks | Sleep regularity will be measured by the validated Chinese version of sleep regularity questionnaire (SRQ), which shows excellent reliability and validity. SRQ consists of six items focusing on two dimensions, circadian regularity and sleep continuity regularity. Each item is rated on a scale ranging from 0 (not at all) to 4 (very much) in terms of the degree to which they agreed with each statement, with higher scores indicating higher sleep regularity. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Severity of depression | From baseline assessment to the end of intervention at 3 weeks | The severity of depression will be measured by the Patient Health Questionnaire - 9 item (PHQ-9). It asks participants how often they experienced depressive symptoms over the past 2 weeks. PHQ-9 comprises 5 categories: 0-4 indicates minimal depression, 5-9 mild depression, 10-14 moderate depression, 15-19 moderately severe depression, and ≥20 severe depression. |
| Severity of anxiety | From baseline assessment to the end of intervention at 3 weeks | The severity of anxiety will be measured by the Generalized Anxiety Disorder - 7 item (GAD-7). The cut-off scores of GAD-7 are: 0-4 indicates minimal anxiety, 5-9 mild anxiety, 10-14 moderate anxiety, and ≥15 severe anxiety. |
| Work and social functioning | From baseline assessment to the end of intervention at 3 weeks | Work and social functioning will be assessed using the Work and Social Adjustment Scale (WSAS), a 5-item instrument in which each item is rated on a 9-point Likert scale (0 = not at all, 8 = very severely). The total WSAS score ranges from 0 to 40, with lower scores indicating better functioning. |
Countries
Hong Kong
Contacts
Primary ContactDanny YU, PhD
Outcome results
None listed