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Study on the clinical effect of Tai Chi massage on subacute non-specific neck pain and the differential expression of serum proteomics

Study on the clinical effect of Tai Chi massage on subacute non-specific neck pain and the differential expression of serum proteomics

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078012
Enrollment
Unknown
Registered
2023-11-27
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-03

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

Conditions

Subacute nonspecific neck pain

Interventions

test team:Tai Chi tuina therapy
control group:wet fomentation therapy
healthy controls:None

Sponsors

Hubei provincial hospital of traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1 with neck pain, stiffness as the main complaint, and in line with the above diagnostic criteria ; 2 aged 18-30 years old, regardless of gender ; 3 neck pain VAS score in 3-5 points ; 4 voluntarily join and sign the informed consent ; note : It is necessary to meet the above four requirements at the same time ;

Exclusion criteria

Exclusion criteria: 1 Previous cervical imaging reports suggest : cervical fusion, skull base depression sign, subluxation, cervical deformity, vertebral instability, etc. 2 have a history of trauma such as cervical spine fracture and dislocation ; 3 neck and shoulder skin damage ; 4 VAS score greater than 5 points, with upper limb radioactive pain, numbness ; 5 cervical vertigo, accompanied by nausea and vomiting during attack ; 6 previous circulation, blood system, tumor, tuberculosis and other diseases ; 7 mental patients ; pregnancy and lactation ; 8 those who are participating in other clinical trials that interfere with this study ; 9 patients with oral analgesic drugs within a week ; 10 did not sign the informed consent ; it was evaluated by researchers not suitable for clinical trials. Note : If any of the above is met, the exclusion criteria are met.

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
NDI;Myoton PRO;Musculoskeletal ultrasound detection;

Countries

China

Contacts

Public ContactCao Biwei

Hubei provincial hospital of traditional Chinese Medicine

caobiwei@hbhtcm.com+86 138 7150 7389

Outcome results

None listed

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