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Not yet recruitingNCT07645911Updated Jun 12, 2026

Gansu Nurses' Health Cohort Study

An observational study in Nurses' Occupational Health, Mental Health and Chronic Diseases, sponsored by LanZhou University. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-12.

Sponsored by LanZhou University · Observational

Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
1,000
Ages
18 Years and older
Sex
All
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Study summary

This study aims to understand the health status, work stress, and occupational exposure in the work environment among nurses in Gansu Province, China. We will collect information through questionnaires and conduct follow-up surveys every two years. The results of this study will help improve working conditions for nurses in the future and provide scientific evidence for developing health protection policies for the nursing workforce.

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Conditions studied

  • Nurses' Occupational Health
  • Mental Health
  • Chronic Diseases
  • Occupational Exposure
  • Reproductive Health

Keywords

  • Nurses, Occupational Health, Questionnaire Survey
  • Nurse health status
  • Nurse Health Cohort Study
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In context

Psychological Well-Being

2,193 studies on the registry are indexed under Psychological Well-Being; 728 are open to participants now.

This study's planned enrollment of 1,000 is above the median of 300 across 358 observational studies indexed under Psychological Well-Being.

Browse Psychological Well-Being studies →

Lead sponsor

LanZhou University is the lead sponsor of 27 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants are clinical nurses from hospitals across 14 prefecture-level cities in Gansu Province, recruited via convenience sampling. Eligible subjects are aged 18 years or older, including both male and female practicing nurses who voluntarily complete self-administered questionnaires.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Age ≥ 18 years;
  2. Able to communicate freely, have the ability to act, and agree to participate in this study.

Exclusion criteria

Exclusion Criteria:

  1. Resigned from the hospital;
  2. Without a nursing license;
  3. Have a history of mental illness or severe cognitive impairment.
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
1,000 participants (estimated)
Patient registry
No

Interventions

  • OtherQuestionnaire Investigation

    Self-reported questionnaire survey for clinical nurses; no drug, operation or other clinical intervention is implemented in this research.

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What researchers measure

Primary outcomes

  1. Occupational health level of clinical nurses

    This study primarily uses the following scales to assess health outcomes among nurses: 1. Morningness-Eveningness Questionnaire, 5-item version; scores 4-25, with higher scores indicating greater morning-type chronotype. 2. Work-Family Balance Scale; scores 14-70, with higher scores indicating greater levels of work-family conflict or facilitation. 3. Practice Environment Scale of the Nursing Work Index; scores 31-124, with higher scores indicating a more supportive work environment. 4. Perceived Stress Scale; scores 0-40, with higher scores indicating greater perceived stress. 5. Maslach Burnout Inventory-Human Services Survey; scores 0-132, with higher scores indicating greater burnout severity. 6. Nurses' Perceived Professional Benefits Scale; scores 33-165, with higher scores indicating higher perceived professional benefits. 7. Yale-Brown Obsessive Compulsive Scale; scores 0-40, with higher scores indicating greater symptom severity.

    Time frame: This is a 5-year observational cohort study with no interventions. Three cross-sectional outcome assessments will be conducted: first from June 2026 to December 2026, second from June 2028 to December 2028, and third from June 2030 to December 2030.

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07645911
Lead sponsor
LanZhou University
Responsible party
Yan Fanghong (Lecturer, LanZhou University) — Principal investigator
First posted
Jun 12, 2026
Start date
Jun 10, 2026 (estimated)
Primary completion
Dec 31, 2031 (estimated)
Completion
Dec 31, 2032 (estimated)
Last update
Jun 12, 2026

Study contacts

Fanghong Yan, PhD
Contact
yanfanghong@163.com
+86-13679295091

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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