The Study of Personalized Health Check-up Programs and Standards for High-altitude Migrant Populations

ConditionHigh Altitude
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCapital Medical University

About this trial

By using wearable devices to monitor and record the physiological data changes and health outcomes (incidence and severity of high-altitude illnesses) of high-altitude migrants at different stages (pre-entry, acute/chronic high-altitude phases, and de-acclimatization phase), and referencing previous cohort studies on high-altitude populations, the study aims to provide a basis for developing personalized health assessment protocols for high-altitude migrants. The formulated assessment protocols and standards will then be validated.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Men and women aged ≥18;

Those living in plains and preparing to move to the plateau for a short-term or medium-term period;

Can understand the research requirements and be willing to sign a written informed consent form (ICF).

Disqualifiers

Past history of contraindicated plateau travel: such as advanced COPD (FEV₁<30% of the expected value or requires continuous oxygen therapy), advanced cystic fibrosis (FEV₁<30% of the expected value or requires continuous oxygen therapy), advanced restricted pulmonary disease (FEV₁<50% of the expected value or requires continuous oxygen therapy), decompensated heart failure, high-risk pregnancy, myocardial infarction or stroke occurred within 90 days, poorly controlled epilepsy, pulmonary hypertension (PASP>90mmHg), sickle cell anemia, unstable angina pectoris, high-risk cerebrovascular abnormalities that have not been treated, etc.

Trial population

Recruit those who live in plains and prepare to move to the plateau in the short term or medium term.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

300 Participants
are grouped into 2 trial groups
Group A: Exploration group
Group B: Verification group

Trial outcomes

Primary outcomes

1

Rates of high altitude sickness and related diseases.

Early diagnosis rates of acute and chronic altitude sickness and related diseases induced or aggravated by the plateau population in migrant plateau populations.

Time frame
through study completion, an average of 3 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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