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A multicenter, unblinded, parallel controlled study on precise evaluation and personalized intervention to improve insomnia relief rate in patients with insomnia disorders

A multicenter, unblinded, parallel controlled study on precise evaluation and personalized intervention to improve insomnia relief rate in patients with insomnia disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074998
Enrollment
Unknown
Registered
2023-08-22
Start date
2023-08-23
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

Insomnia

Interventions

Precision intervention group:On the basis of maintaining the original treatment plan, the intervention group patients are recommended to receive personalized treatment by doctors based on the results
Conventional treatment group:Choose appropriate clinical diagnosis and treatment plans based on the patient s condition

Sponsors

Nanfang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Member unit: Hospital level 2A or above; A dedicated person is responsible for coordinating the work; Team members need to obtain a GCP certificate. Patient: Currently meets the DSM-5 diagnostic criteria for insomnia disorders; Patients with stable physical diseases, mental disorders and Sleep disorder, including those taking drugs (such as antihypertensive drugs, antidepressants, benzodiazepines, etc.), that is, patients can continue to accept the existing treatment scheme (Treat As Usual, TAU); 18-60 years old; Can understand and comply with the research plan; Informed consent can be provided.

Exclusion criteria

Exclusion criteria: Member unit: unable to pass ethics; Unable to receive regular training; Unable to promote and apply new prevention and control systems. Patient: Pregnant or lactating women; Suffering from severe intellectual disabilities or physical illnesses; Other situations that are not suitable for inclusion in the study.

Design outcomes

Primary

MeasureTime frame
Insomnia relief rate;

Secondary

MeasureTime frame
Treatment satisfaction;

Countries

China

Contacts

Public ContactBin Zhang

Nanfang Hospital of Southern Medical University

zhang73bin@hotmail.com+86 135 2780 7502

Outcome results

None listed

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