A Cross-sectional Study on the Impact of Shift Work on Diastolic Dysfunction in Healthcare Workers
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Diastolic Dysfunction. Basic parameters: No limits · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The goal of this observational cross-sectional study is to assess the prevalence of left ventricular diastolic dysfunction and identify associated risk factors in health-care workers of various ages and both sexes. The main questions it aims to answer are: What is the prevalence of diastolic dysfunction among healthcare workers? Which occupational, lifestyle, or clinical factors are associated with abnormal diastolic function in this population? Researchers will compare health-care workers who dont need night shift with those who have to. Participants will: Complete questionnaires regarding demographic information, work schedules, lifestyle factors, and medical history. Undergo echocardiographic examination to assess diastolic function. Receive basic vital sign by ambulatory blood pressure monotoring.
Primary outcome measures
- diastolic dysfunction [Time frame: 2026/01~ 2026/12]
- diastolic dysfunction [Time frame: from january 2026 to December 2026]
Eligibility criteria
Inclusion Criteria: Healthcare workers at our hospital
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07331233 · 202510163RINE