Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07084701

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Tianjin Medical University General Hospital

Tianjin, China

Actively Recruiting

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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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