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Study on the effect of Chen's Tai Chi on chronic non-specific neck pain and surface electromyographic characteristics

Study on the effect of Chen's Tai Chi on chronic non-specific neck pain and surface electromyographic characteristics

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080609
Enrollment
Unknown
Registered
2024-02-02
Start date
2024-02-16
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Chronic Non-specific Neck Pain

Interventions

Experimental group:The Essential 18 Forms of Chen's Tai Chi
Control group:Lectures on health related to neck pain

Sponsors

Shanghai University of Sport
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Referring to the "Diagnostic and Therapeutic Efficacy Standards for Traditional Chinese Medicine (2012 Edition)" formulated by the National Administration of Traditional Chinese Medicine and the Clinical Practice Guidelines for Neck Pain (2017 Edition) published by the American Physical Therapy Association, and taking into account the characteristics of this study, the following inclusion and exclusion criteria are formulated: 1. Aged 18-55, able to understand Mandarin and read and write Simplified Chinese on their own; 2. The duration of neck and shoulder back pain is = 3 months (including recurrent episodes); 3. Voluntarily participate and be interested in Tai Chi; 4. Sign the informed consent form for entering the study.

Exclusion criteria

Exclusion criteria: 1. people with neck pain accompanied by compression of nerve roots, spinal cord, vertebral artery, sympathetic nerve, etc. 2. persons with neck pain caused by a combination of other bone and joint diseases, trauma, or surgery 3. those with serious heart, lung, liver, kidney, hematopoietic system diseases and/or serious psychiatric diseases 4. women who are breastfeeding, pregnant, or preparing for pregnancy 5. who have undergone, are undergoing, or intend to undergo neck exercise training or clinical treatment during this study 3 months prior to enrollment 6. those who are taking or intend to take pain medication during this study 7. those with a history of serious trauma and surgery within 6 months.

Design outcomes

Primary

MeasureTime frame
pain pressure threshold, PPT;active range of motion, AROM;co-contraction ratio, CCR;

Secondary

MeasureTime frame
Quality of life assessment;Assessment of cervical spine dysfunction;Neck pain intensity assessment;body mass index,BMI;

Countries

China

Contacts

Public ContactLiu Jing

Shanghai University of Sport

liujing_j3@163.com+86 150 2661 2695

Outcome results

None listed

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