Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Electroacupuncture for neck stiffness in chronic neck pain

Official title: The Immediate Effect of Electroacupuncture on Neck Muscle Stiffness in Individuals With Chronic Neck Pain

Run by The Hong Kong Polytechnic University · NCT07741227 · Data updated 2026-11-12

This study tests whether a 20-minute electroacupuncture session can change neck muscle stiffness right away in adults with chronic neck pain, using ultrasound to measure the effect.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment66 (estimated)
SponsorThe Hong Kong Polytechnic University
Academic / other
Locations1 site (Hong Kong)
StatusRecruiting
StartedMay 1, 2026
Main results expectedSeptember 30, 2026
Study endsOctober 30, 2026
Registry record updatedAugust 24, 2026
Trial IDNCT07741227 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–65 with non-specific chronic neck pain (≥3 months) and average pain ≥3/10 in the past week, localized to the posterior neck region.

Probably not a fit

Individuals with specific neck pathologies, recent neck surgery, or contraindications to acupuncture may not experience benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized, single-blind, placebo-controlled trial compares true electroacupuncture to sham electroacupuncture in adults with non-specific chronic neck pain lasting at least 3 months. The primary outcome is immediate changes in neck muscle stiffness measured by Shear Wave Elastography after a single 20-minute session. Participants are 18 to 65 years old, with average pain of at least 3/10 in the past week, and pain localized to the posterior neck area. The study uses objective ultrasound-based biomechanics to provide high-quality evidence on the immediate effects of electroacupuncture. Conducted at The Hong Kong Polytechnic University, the trial aims to clarify whether the electrical stimulation component offers measurable biomechanical benefits beyond sham treatment.

Why it matters

Potential benefit: If successful, patients may experience immediate improvements in neck muscle stiffness after electroacupuncture.

How similar studies have gone: Other studies using electroacupuncture have shown mixed or variable immediate biomechanical effects; this trial adds objective SWE measurements to clarify benefit.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Aged 18-65 years
2. Chronic non-specific neck pain persisting for ≥3 months
3. Average pain intensity ≥3 on a 0-10 Numeric Rating Scale over the past week
4. Pain primarily located in the posterior cervical region, which may radiate to the upper trapezius muscles
5. Able to provide informed consent and sufficient language proficiency to complete questionnaires

Exclusion Criteria:

1. Specific pathological causes for neck pain (cervical radiculopathy or myelopathy, fracture, infection, tumour, systemic rheumatic disease)
2. History of neck or shoulder surgery
3. Contraindications to acupuncture (severe needle phobia, bleeding disorders, pregnancy)
4. Received acupuncture or other physical therapy for neck pain within the past 6 months

Where it's running

  • The Hong Kong Polytechnic University
    Hong Kong, Hong Kong
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.