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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05396729
Other study ID # XJH-A-20220525
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 30, 2022
Est. completion date April 2023

Study information

Verified date November 2022
Source Air Force Military Medical University, China
Contact Zhihong Lu
Phone +8613891975018
Email deerlu23@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Sleep disorder is common in people going to plateau. Acupuncture and related techniques could be used for treatment of sleep disorder. In this trial the effect of transcutaneous electrical acupoint stimulation on sleep disorder in people going to plateau will be investigated.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date April 2023
Est. primary completion date April 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Age from 18 to 40 years - first time to the plateau (altitude =3000 meters) Exclusion Criteria: - those who live in area with altitude =2000 meters, or travel to plateau in the last half year - history of insomnia - patients with contraindication to transcutaneous electrical stimulation, including skin damage, infection or implantable electrical device - difficulty in verbal communication - history of taking medicine to improve sleep during the last 3 months - regular daily intake of large dose of tea or coffee (>400 mg of caffeine) - suspected or existed abuse of drug or alcohol - disease that influence sleep such as chronic pain

Study Design


Related Conditions & MeSH terms


Intervention

Device:
transcutaneous electrical acupoint stimulation
Electrodes are placed at acupoints and connected to the stimulator. Electrical stimulation is given for 30 minutes, twice a day for 3 days.

Locations

Country Name City State
China Xijing hospital Xi'an Shaanxi

Sponsors (1)

Lead Sponsor Collaborator
Air Force Military Medical University, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary total sleep time in 5 days from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary sleep latency on the fifth day from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary sleep efficiency on the fifth day sleep efficiency=total sleep time/total recording time from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary number of awake on the fifth day from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary Pittsburgh sleep quality index on the fifth day from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary Score of Cognition Assessment on the third day cognition assessment is done using Rey Auditory Verbal Learning Test from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary lowest saturation of pulse oxygenation on the fifth day from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary highest systolic blood pressure on the fifth day from arrived at plateau to 5 days after arrival, in a total of 5 days
Secondary highest heart rate on the fifth day from arrived at plateau to 5 days after arrival, in a total of 5 days
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