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Clinical effects and brain function study of Tuina on chronic insomnia

Clinical effects and brain function study of Tuina on chronic insomnia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075293
Enrollment
Unknown
Registered
2023-08-31
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

Chronic Insomnia

Interventions

Control Group:Conventional head and face tuina
Experimental Group:In addition to the control group's intervention tuina method, the back bladder meridian points were added.

Sponsors

Shanghai Hudong Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 to 65 years old. Gender is not limited 2. Meet diagnostic criteria and PSQI score of 6 or above 3. Able to communicate well with researchers, cooperate and follow the test requirements 4. Those who voluntarily participate in the research and sign the informed consent form

Exclusion criteria

Exclusion criteria: 1. Those with serious organic diseases such as cardiovascular, lung, liver, kidney and hematopoietic system diseases 2. History of serious neurological or psychiatric disease 3. Have a history of infectious diseases and genetic diseases 4. Participated in any other clinical trials within one month of the screening date 5. Pregnant and lactating patients 6. People who cannot cooperate with rs-fMRI and fNIRS examinations

Design outcomes

Primary

MeasureTime frame
PSQI;

Secondary

MeasureTime frame
Self-Rating Anxiety Scale;Self-Rating Depression ;

Countries

China

Contacts

Public ContactPing Lu

Shanghai University of Traditional Chinese Medicine

lupinglim@163.com+86 139 0188 7749

Outcome results

None listed

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