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Adaptive study of PRO scales in different insomnia populations

Adaptive study of PRO scales in different insomnia populations

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067745
Enrollment
Unknown
Registered
2023-01-20
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

insomnia

Interventions

Observation group:N/A

Sponsors

Xiyuan Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The age of the subjects is 18-80 years old, and the gender is not limited; 2. Meet the above diagnostic standards of traditional Chinese and Western medicine; 3. Understand the purpose of research, understand the purpose of research, and be able to truthfully assess their psychological condition; 4. Voluntary testing.

Exclusion criteria

Exclusion criteria: 1. Have been clearly diagnosed with anxiety or depression in the past month; 2. Cognitive dysfunction, unable to accurately understand the test description and complete the questionnaire; 3. Patients who are participating in other clinical trials; 4. Unwillingness to be tested; 5. The subject terminates by himself, if he cannot continue to respond to the scale; 6. The scale filling process is interrupted for more than 2 hours.

Design outcomes

Primary

MeasureTime frame
Scales;Reliability;validity;Reactivity;

Countries

China

Contacts

Public ContactZi Mingjie

Xiyuan Hospital, China Academy of Chinese Medical Sciences

drzimingjie@126.com+86 136 2105 2996

Outcome results

None listed

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