The study of sleep quality for medical personnel in Hubei

The follow-up study of sleep and stress status among medical personnel in Hubei

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100054893

Enrollment

Unknown

Registered

2021-12-28

Start date

2021-04-01

Completion date

Unknown

Last updated

2022-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insomnia, stress

Interventions

Stress group:No

Health control group:No

Eligibility

Sex/Gender

All

Age

18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Subjects have not taken benzodiazepine or non-benzodiazepine sedative hypnotics within the past month; 3. Subject have provided a written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with concomitant cardiovascular, lung, liver, kidney, hematopoietic, and other severe primary diseases, and those with severe organic brain disease and mental illnesses; 2. Patients with a history of alcoholism or use of other psychoactive substances; 3. Pregnant or breastfeeding women.

Design outcomes

Primary

Measure	Time frame
Sleep efficiency;ISI (Insomnia Severity Index);	—

Countries

China

Contacts

Public ContactZhou Yiqing

Shanghai Putuo Mental Health Center

zhouyiqing666@126.com+86 13917826752

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026