Actively Recruiting
Electroacupuncture and Cupping for Shoulder Tendinitis
Led by University of Medicine and Pharmacy at Ho Chi Minh City · Updated on 2026-04-22
54
Participants Needed
2
Research Sites
37 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to evaluate the effectiveness of electroacupuncture combined with vacuum cupping therapy in treating simple periarthritis of the shoulder associated with the traditional medicine syndrome of Qi stagnation and blood stasis. Shoulder periarthritis is a common condition that causes pain, stiffness, and limited movement of the shoulder due to injury or inflammation of the muscles, tendons, ligaments, and surrounding soft tissues. It can interfere with daily activities such as dressing, lifting objects, sleeping, and working. Electroacupuncture is commonly used to relieve shoulder pain and improve shoulder function. Vacuum cupping therapy is another non-drug treatment that may help improve blood circulation, reduce muscle tightness, decrease pain, and improve mobility. However, there is currently limited evidence about whether combining electroacupuncture with vacuum cupping provides better results than electroacupuncture alone in patients with shoulder periarthritis and Qi stagnation-blood stasis syndrome. This study is being conducted to determine whether the combined treatment is more effective and safe. A total of 54 participants with simple shoulder periarthritis and Qi stagnation-blood stasis syndrome will be enrolled in the study. Participants will be randomly assigned to one of two groups: Group 1: treatment with electroacupuncture alone. Group 2: treatment with electroacupuncture combined with vacuum cupping therapy. All participants will also receive advice on shoulder exercises, posture, and daily activities to support recovery. Treatments will be performed by licensed traditional medicine practitioners. Each participant will take part in the study for two weeks. Assessments will be performed before treatment, after one week, and after two weeks. The study will evaluate: Pain intensity using the Visual Analogue Scale (VAS). Shoulder pain and disability using the Shoulder Pain and Disability Index (SPADI). Shoulder range of motion using the McGill-McRomi Range of Motion Index. Any side effects or unwanted events related to treatment. Possible benefits of participating in this study include reduced shoulder pain, improved movement and daily function, and close monitoring by health care professionals. Participants may also benefit from receiving non-drug therapies at no cost during the study period. The findings of this research may help improve future treatment options for patients with shoulder pain. Possible risks of electroacupuncture include mild pain at the needle site, minor bleeding, bruising, dizziness, or fainting. Possible risks of vacuum cupping include temporary discomfort, skin redness, bruising, or mild pain in the treated area. These side effects are usually mild and temporary. If any unexpected problem occurs, participants will receive prompt medical attention. Participation in this study is completely voluntary. Participants may refuse to join or may withdraw from the study at any time without affecting their usual medical care. All personal information collected during the study will remain confidential and will only be used for research purposes.
CONDITIONS
Official Title
Electroacupuncture and Cupping for Shoulder Tendinitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients between 18 and 70 years old.
- Pain intensity score on the Visual Analogue Scale (VAS) between 4 and 7.
- Diagnosis of rotator cuff and/or long head of the biceps tendonitis according to Ministry of Health of Vietnam guidelines.
- Mechanical pain increasing during movements such as arm abduction or raising.
- Presence of tender points at the long head of the biceps tendon or supraspinatus tendon.
- Pain increasing during resisted contraction tests like the Jobe test or Palm-up test.
- No limitation in passive shoulder range of motion.
- Ultrasound showing hypoechoic tendon or calcification evidence.
- No motor weakness or paralysis.
- Diagnosis of traditional Chinese medicine syndrome "Qi Stagnation and Blood Stasis".
You will not qualify if you...
- Patients who do not agree to participate.
- Diagnosis of pseudo-paralysis, acute calcific periarthritis, or frozen shoulder.
- Shoulder pain caused by cervical nerve root lesions.
- Shoulder pain from apical lung tumors, coronary artery disease, or myocardial infarction.
- Joint lesions from infection, tuberculosis, or rheumatoid arthritis.
- Bone problems including fractures, dislocations, or osteonecrosis of the humeral head.
- Shoulder dysfunction due to stroke or hemiplegia.
- Pregnant women.
- Patients with mental illness.
- Contraindications for vacuum cupping like acute skin inflammation, open wounds, or alcohol use.
- Contraindications for electroacupuncture including cardiac pacemakers, heart failure, or local skin ulcers.
- Current participation in another intervention study.
- Use of painkillers or muscle relaxants within the last week.
- Use of anticoagulants or history of hemophilia.
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Le Van Thinh Hospital
Ho Chi Minh City, Vietnam, 71322
Actively Recruiting
2
Ho Chi Minh City Orthopedic and Rehabilitation Hospital
Ho Chi Minh City, Vietnam, 72121
Actively Recruiting
Research Team
H
HUY HOANG LAM, Doctor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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