Actively Recruiting
Effects of Non-Invasive Superficial Craniocervical Lymphatic Drainage (NSCLD) on Memory and Cognitive Function in Adults With Sleep Deprivation: A Proof-of-Concept Study
Led by Tao Liu · Updated on 2026-01-13
30
Participants Needed
1
Research Sites
63 weeks
Total Duration
On this page
Sponsors
T
Tao Liu
Lead Sponsor
T
Tianjin Medical University General Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This Effects of Non-Invasive Superficial Craniocervical Lymphatic Drainage (NSCLD) on Memory and Cognitive Function in Adults with Sleep deprivation: A Proof-of-Concept Study aims to investigate the effects of Non-Invasive Superficial Craniocervical Lymphatic Drainage (NSCLD) on memory and cognitive function in adults experiencing sleep deprivation(SD). Given the known impact of SD on cognitive performance, this study seeks to explore whether NSCLD, as a non-invasive intervention, can mitigate the cognitive impairments associated with SD.
CONDITIONS
Official Title
Effects of Non-Invasive Superficial Craniocervical Lymphatic Drainage (NSCLD) on Memory and Cognitive Function in Adults With Sleep Deprivation: A Proof-of-Concept Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- College student aged 18 years or older who has passed a standardized entrance exam
- No failed exams during course of study
- Experiencing sleep deprivation
- In good health with no mental or psychological disorders
- No recent use of medications affecting memory or cognition
- Voluntary participation and able to complete cognitive and memory tests
- Provided informed consent
You will not qualify if you...
- Pregnant or breastfeeding women
- Acute or chronic medical conditions such as severe hypertension, diabetes, or cardiovascular disease
- History of craniocervical trauma or surgery
- Current use of sedative or anxiolytic medications affecting sleep or cognition
- Unable to follow procedures or complete assessments
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Tianjin Medical University General Hospital
Tianjin, China
Actively Recruiting
Research Team
T
Tao Liu, MD
CONTACT
Y
Yuezheng Dou
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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