Skip to content

Efficacy of tuina versus proprioceptive neuromuscular facilitation (PNF) in patients with NCNP: study protocol for a randomized controlled trial

Efficacy of tuina versus proprioceptive neuromuscular facilitation (PNF) in patients with NCNP: study protocol for a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2023000061
Enrollment
Unknown
Registered
2023-12-04
Start date
2023-10-15
Completion date
Unknown
Last updated
2023-12-18

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

Conditions

Nonspecific chronic neck pain

Interventions

the PNF and tuina combined group:The combined group will first receive 30 minutes of PNF technique followed by 30 minutes of tuina therapy, thus the total time will be approximately 60 minutes. PNF te
the PNF group:Group 1: PNF technique 1. PNF stretching for approx. 20 min: Hold-Relax-Antagonist Contraction (HRAC) stretching technique is used: stretching the upper trapezius, scapularis, sternoclei
the tuina group:Group 2: Tuina group: TCM Tuina intervention was used for 4 weeks, 3 times a week, 30 min each time. The following techniques were included: pressing and kneading to loosen tendons, p

Sponsors

Beijing University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1.Male or female with age range: 18-30 years; 2.Complaint of neck pain (VAS = 30mm) including presence of pain, stiffness, and restricted movement in the occipital, neck, shoulder, or scapular regions. 3.Physical examination of the cervical spine does not exhibit indications of nerve root compression. 4.Duration of symptoms lasting for a minimum of three months. 5.Voluntary participation in the study and provision of informed consent through signature.

Exclusion criteria

Exclusion criteria: 1.Being treated with, or have been treated in the past 1 month with, another effective method for NCNP; 2.Patients with neck pain accompanied by compression of nerve roots, spinal cord, vertebral arteries, sympathetic nerves, etc; 3.Patients with localised skin breakdown, skin disease or skin sensory impairment; 4.Pregnant and breastfeeding women; 5.Patients with cognitive impairment, sensory aphasia, severe visual or hearing impairment; 6.Patients with a combination of cervical fractures, dislocations, tumours, infections, rheumatoid and other specific causes of neck pain; 7.Patients with pain in more than 3 areas other than the neck and shoulder area; 8.Patients with a combination of serious medical conditions such as cardiovascular, haematopoietic and endocrine diseases.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale (VAS) ;Neck Disability Index (NDI);

Secondary

MeasureTime frame
Cervical active joint mobility;Muscle Physical Properties Test;

Countries

China

Contacts

Public ContactXiangyu Zhu

Beijing University of Traditional Chinese Medicine

116491992@qq.com+86 188 1036 1589

Outcome results

None listed

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