- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06557928
Protocol for Evaluating Physiological and Psychological Adaptation Mechanisms in Tibetan Plateau Environments
August 14, 2024 updated by: DONG WU, Peking Union Medical College Hospital
Protocol for Evaluating Physiological and Psychological Adaptation Mechanisms in Tibetan Plateau Environments: A Clinical Study of Doctors From Peking Union Medical College Hospital
This study is a single-center prospective observational study.
It plans to use a series of physiological and medical instruments and international common physiological and psychological questionnaires.
To dynamically detect the changes of physiological and psychological adaptability of doctors in Peking Union Medical College Hospital before leaving Beijing, 1-7 days after arriving at the plateau in Tibet during the acute phase of plateau hypoxic stress, 2 weeks, 3 months, 6 months, 12 months after staying in Tibet during the chronic phase of plateau hypoxic stress, and after returning to Beijing.
Study Overview
Study Type
Observational
Enrollment (Estimated)
17
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Beijing, China
- Peking Union Medical College Hospital
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Doctors in Tibet from Peking Union Medical College Hospital
Description
Inclusion Criteria:
- Healthy individuals aged 20-65 years
- They can sign a written informed consent and is willing to cooperate
- They have the qualification to aid Tibet and meet the basic requirements of physical examination for aid to Tibet
Exclusion Criteria:
- Age less than 20 years or more than 65 years
- Unable to sign a written informed consent or unwilling to cooperate
- They do not have the qualification for supporting Tibet or do not meet the basic requirements of medical examination for supporting Tibet
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Doctors to Tibet from Peking Union Medical College Hospital in 2024
|
Measurement of multiple physiological indicators and psychological status and multi-omics study
|
|
Doctors to Tibet from Peking Union Medical College Hospital in 2025
|
Measurement of multiple physiological indicators and psychological status and multi-omics study
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
help understand the physiological mechanisms and psychological changes of hypoxic adaptation
Time Frame: 2024-5-27~2026-12-1
|
This study is expected to increase our understanding of the physiological mechanisms and psychological changes of hypoxic adaptation mainly through analysis of multi-omics.
|
2024-5-27~2026-12-1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 17, 2024
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2027
Study Registration Dates
First Submitted
August 14, 2024
First Submitted That Met QC Criteria
August 14, 2024
First Posted (Actual)
August 16, 2024
Study Record Updates
Last Update Posted (Actual)
August 16, 2024
Last Update Submitted That Met QC Criteria
August 14, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2022-I2M-1-003
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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