Effects of Acute Sleep Deprivation on Individuals With Different APOE Genotypes
Recruiting now · Not applicable
Conditions studied: Sleep, Sleep Deprivation
In brief
This study aims to investigate the effects of 24-hour acute sleep deprivation on plasma Alzheimer's disease biomarkers and multi-omics in individuals with different APOE genotypes, to elucidate the potential role of acute sleep deprivation in AD risk.
Key facts
- Study ID
- NCT07085754
- Run by
- Yuhui Qiu
- People needed
- 60
- Starts
- 2025-08-08
- Expected to finish
- 2026-12-31
- Last updated by the study team
- 2025-12-24
Who can join
Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18-40 years, gender not limited
- Healthy (with no clinically significant abnormal findings in the physical examination report or self-reporting as healthy) and not on medications
- Cognitively normal (Mini-Mental State Examination (MMSE) score > 28)
- Sleep duration of 7-9 hours per night, good sleep quality (Pittsburgh Sleep Quality Index (PSQI) ≤ 5 points)
- Written informed consent, voluntarily participate in this study, and be able to cooperate with the physician to complete the clinical study
You may not qualify if…
- Presence of day-night sleep reversal
- Shift work within the past 6 months
- Travel across time zones or experience of jet lag within the past three weeks
- Current smoking or nicotine use; alcohol consumption exceeding five standard units per week (one standard alcohol unit is defined as 10 mL [or 8 g] of pure alcohol)
- Consumption of strong tea, coffee, or caffeine-containing foods and beverages within one week before study participation
- Family history of early-onset dementia
- Self-Rating Depression Scale (SDS) score ≥ 53, Self-Rating Anxiety Scale (SAS) score ≥ 50
- Female participants who are currently pregnant or breastfeeding
- Individuals who need to drive or operate vehicles or machinery during the study period
Where it is running
- Guangdong Provincial Hospital of Chinese Medicine — Guangzhou, Guangdong, China (enrolling)
Full record on ClinicalTrials.gov
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