The Efficacy of Thread Embedding Acupuncture on Pain Score, Neck Disability Index, and Pressure P… (NCT05987683) | Clinical Trial Compass
CompletedNot Applicable
The Efficacy of Thread Embedding Acupuncture on Pain Score, Neck Disability Index, and Pressure Pain Threshold for Myofascial Pain Therapy in the Upper Trapezius Muscle
Indonesia44 participantsStarted 2023-08-21
Plain-language summary
Myofascial pain is characterized by myofascial trigger points, considered as a major cause of neck and shoulder pain in the working population. Thread-embedding acupuncture is a new acupuncture modality that can provide long-term stimulation aimed at prolonging its therapeutic effect that is similar to conventional acupuncture, such as analgesic effects. The goal of this randomized controlled trial is to evaluate and compare the effects of thread-embedding acupuncture and sham thread-embedding acupuncture as a therapy for myofascial pain in the upper trapezius muscle. The primary aim of this study is to investigate whether thread-embedding acupuncture therapy gives better and last longer results for myofascial pain of the upper trapezius muscle than sham thread-embedding acupuncture.
Who can participate
Age range
18 Years – 59 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Male or female aged 18-59 years.
* Subject with myofascial pain in the upper trapezius muscle.
* VAS score of 30-70 mm from 100 mm during activities (everyday activities or light exercise).
* Pain \> 3 months.
* Willing to participate in this research to completion and sign informed consent.
Exclusion Criteria:
* Fibromyalgia.
* Have had cervical spine surgery.
* Have done Dry needling therapy on the upper trapezius muscle in the last 9 days
* Have done thread acupuncture on the upper trapezius muscle in the last 6 months.
* Have performed pharmacopuncture on the upper trapezius muscle in the last 6 months.
* VAS score is more than 70 mm than 100 mm at resting.
* History of anti-inflammatory drug treatment in the previous 2 weeks.
* History of intra-articular steroid injections in the previous 3 months.
* There is a tumor, wound, or skin infection at the needle insertion area.
* Fever (≥ 37.5 oC).
* There is a hypersensitivity reaction in previous acupuncture therapy (metal allergy, severe atopy, keloids, or other skin hypersensitivity).
* Suffering from a blood disorder or taking blood thinners (anti-platelet or anti-coagulant drugs).
* Have a heart condition or uncontrolled diabetes.
* Blood glucose level (GDS) ≥200 mg/dL is checked by capillary blood using a glucometer.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Visual Analog Scale
Timeframe: before treatment (baseline) and 3 days, 1 week, 4 weeks, 8 weeks after treatment