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Development and Clinical Applicability Evaluation of an Expert Consensus on Meridian Sinew Syndrome Differentiation in Tuina Therapy for Non-Specific Neck Pain

Development and Clinical Applicability Evaluation of an Expert Consensus on Meridian Sinew Syndrome Differentiation in Tuina Therapy for Non-Specific Neck Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000444
Enrollment
Unknown
Registered
2026-03-03
Start date
2025-12-24
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Non-specific neck pain

Interventions

Meridian Sinew Node Tuina Treatment Group:The meridian sinew node of the Foot Shaoyin Meridian at the knee region on the affected side (determined by patient-reported symptoms or more pronounced palpa
Meridian Sinew Node TEAS Treatment Group :The meridian sinew node of the Foot Shaoyin Meridian at the knee region on the affected side was selected and localized by palpation. TEAS treatment was then

Sponsors

Affiliated Hospital of Xiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosed with non-specific neck pain of the Foot Taiyin Meridian Sinew type according to the Neck Pain: Revision 2017clinical practice guidelines and existing expert consensus ; (2) Aged between 18 and 65 years, regardless of gender; (3) Visual Analog Scale (VAS) pain score =3 during cervical extension; (4) Pain episodes lasting more than 30 minutes, occurring at least once per month; (5) No prior acupuncture, tuina, massage, or other neck-related treatments within 7 days before recruitment; (6) Willing and able to comply with intervention and follow-up assessments; (7) Agreement to refrain from other relevant treatments (including muscle relaxants) during the study period; (8) Capable of providing written informed consent.

Exclusion criteria

Exclusion criteria: (1) Exclusion of specific neck pain, such as pain caused by cervical fractures, postoperative pain from cervical spine surgery, or cervical dislocation. (2) Cervical spine tumors or tuberculosis. (3) History of trauma or surgery to the neck and head. (4) Patients with other severe comorbid conditions. (5) Presence of other uncertain factors? that may compromise the data integrity of the subjects in this study. (6) Participation in other concurrent interventions? that may interfere with the outcomes of this trial during the study period.

Design outcomes

Primary

MeasureTime frame
Neck Pain VAS Score;Active Range of Motion of Cervical Extension;

Secondary

MeasureTime frame
Pressure pain threshold (PPT) at the distal treatment meridian sinew node and the patient's neck pain area;Soft Tissue Tension at the distal treatment meridian sinew node and the patient's neck pain area;

Countries

People's Republic of China

Contacts

Public ContactJing Chen

Affiliated Hospital of Xiangnan University

chenjing010@126.com+8618075537186

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026