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NCT Number: NCT07545785

Electroacupuncture and Cupping for Shoulder Tendinitis

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.

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Key information

Conditions

Shoulder Tendinopathy Rotator Cuff Injuries Rupture Shoulder Injuries Shoulder Tendinitis Tendon Injuries Wounds and Injuries

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ho Chi Minh City Orthopedic and Rehabilitation Hospital, Ho Chi Minh City, Vietnam

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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 the guidelines issued by the Ministry of Health of Vietnam.
  • Mechanical pain that increases during movements such as abduction or raising the arm.
  • Presence of tender points at the long head of the biceps tendon or supraspinatus tendon .
  • Pain that increases during resisted contraction tests, such as the Jobe test or Palm-up test.
  • Absence of limitation in the passive range of motion of the shoulder.
  • Ultrasound findings showing a hypoechoic tendon or evidence of calcification.
  • Absence of motor weakness or paralysis.
  • Diagnosis of the TCM syndrome "Qi Stagnation and Blood Stasis"

Exclusion criteria

  • Patients who do not agree to participate in the study.
  • Diagnosis of pseudo-paralysis, acute calcific periarthritis, or frozen shoulder.
  • Shoulder pain caused by cervical nerve root lesions.
  • Shoulder pain originating from apical lung tumors, coronary artery disease, or myocardial infarction.
  • Specific joint lesions caused by infection, tuberculosis, or rheumatoid arthritis.
  • Bone pathologies including fractures, dislocations, or osteonecrosis of the humeral head.
  • Shoulder dysfunction resulting from stroke or hemiplegia.
  • Women who are pregnant.
  • Patients with mental illness.
  • Contraindications for vacuum cupping, such as acute skin inflammation, open wounds, or alcohol consumption.
  • Contraindications for electroacupuncture, including cardiac pacemakers, heart failure, or local skin ulcers.
  • Current participation in another intervention study.
  • Use of painkillers, muscle relaxants, or within the last week.
  • Use of anticoagulants or a history of hemophilia.

Treatment and study plan

electroacupuncture

Procedure

Intervention Description: Electroacupuncture Electroacupuncture is administered using the KWD-808I device and sterile, single-use needles (0.30 x 25 mm). The protocol targets a standardized set of acupoints: LI15 (Jianyu), LI14 (Binao), LI16 (Jugu), SI9 (Jianzhen), SI11 (Tianzong), LU1 (Zhongfu), LU2 (Yunmen), GB21 (Jianjing), and BL17 (Geshu).

Distinguishing Technical Details:

Sensation: Needles are inserted to achieve the "De Qi" sensation (aching, heaviness, or distension).

Electrode Pairing: Electrodes are connected in specific pairs: LU1-LU2, LI15-LI16, and SI11-SI9.

Waveform & Frequency: A continuous wave at a 10Hz frequency is used. Intensity is titrated to the patient's maximum comfortable tolerance (distension without sharp pain).

Regimen: 20 minutes per session, daily for 10 sessions over 2 weeks (excluding weekends).

All procedures are performed by licensed Traditional Medicine physician physicians with over 5 years of experience

Other names: Vacuum Cupping Therapy

Vacuum Cupping Therapy

Procedure

Vacuum Cupping Therapy (VCT) VCT uses 4.5 cm diameter cups and a manual pump to create negative pressure. Standardized procedure: Medium suction force (3 manual pumps) is applied for 5 minutes per session.

Treatment sequence: VCT is performed first, followed by a 10-minute rest period before electroacupuncture.

Acupoint selection: Targets Jianyu (LI15), Quyuan (SI13), Tianzong (SI11), and Naoshu (SI10) on the affected shoulder, plus bilateral Geshu (BL17).

Regimen: 3 sessions over a 2-week period with 3-day intervals. Safety: Vaseline is applied to cup rims to ensure a seal and prevent skin irritation.

All procedures are conducted by licensed Traditional Medicine physicians with at least 5 years of experience

Primary outcomes

  1. Visual Analogue Scale

    Time frame: From enrollment to the completion of the 2-week treatment period, with assessments conducted at baseline (T0), after 1 week of intervention (T1), and after 2 weeks of intervention (T2).

    The Visual Analogue Scale (VAS) is a validated tool used to quantify pain intensity. It consists of a 10cm horizontal line where the 0 cm mark represents "no pain" and the 10 cm mark represents the "worst pain imaginable".

    How the measure is taken: Participants are instructed to mark a single point on the line that best reflects their current level of shoulder pain. The researcher then measures the distance from the 0 cm starting point to the patient's mark in centimeters to obtain a numerical score.

    Pain Level Definitions:

    No pain (0 cm). Mild (1-3 cm): Slight pain that does not significantly interfere with concentration.

    Moderate (4-6 cm): Noticeable pain that may interfere with daily activities, though the patient can still work.

    Severe (7-10 cm): Distressing pain that significantly limits daily activities and affects sleep.

Secondary outcomes

  1. Shoulder Pain and Disability Index - SPADI.

    Time frame: Assessment Schedule: Data is collected at three time points: baseline (T0), after 1 week (T1), and after 2 weeks (T2) of the intervention.

    The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire containing 13 items used to assess shoulder pathology. It is divided into two subscales: Pain (5 items) and Disability (8 items).

    How it is measured: Participants rate their pain and difficulty with daily activities (e.g., washing hair, putting on a shirt) on a scale of 0 to 10, where 0 represents "no pain/no difficulty" and 10 represents "worst pain/requires help".

    Scoring Criteria: Subscale scores are averaged and converted into a total percentage score (0-100%). A higher percentage indicates greater pain and more significant functional impairment

  2. McGill Range of Motion Index - McGill-McRomi.

    Time frame: From enrollment to the completion of the 2-week treatment period, with assessments conducted at baseline (T0), after 1 week of intervention (T1), and after 2 weeks of intervention (T2).

    The McGill Range of Motion Index: provides an objective assessment of the shoulder's functional movement capacity without requiring specialized equipment. Record the maximum range of motion achieved in three movements: shoulder abduction, internal rotation, and external rotation.

    Criteria: Results are categorized into 4 grades:

    Grade 0: No limitation (e.g., Abduction >150°). Grade 1: Mild limitation (e.g., Abduction 101-150°). Grade 2: Moderate limitation (e.g., Abduction 51-100°). Grade 3: Severe limitation (e.g., Abduction 0-50°).

  3. Adverse Events

    Time frame: Adverse events are monitored throughout the 2-week intervention

    Adverse events are monitored throughout the 2-week intervention and recorded as qualitative data (Yes/No) based on clinical observation and patient reports

    . Criteria for Electroacupuncture: Fainting: Occurs if a patient feels dizzy, pale, or breaks into a cold sweat during needling.

    Local Trauma: Includes minor bleeding or bruising at the needle site, or the rare risk of a broken needle.

    Infection: Monitoring for redness or swelling at acupoints.

    Criteria for Vacuum Cupping:

    Bruising: Skin discoloration from suction; while common, it is monitored if severe or persistent.

    Unbearable Pain/Tension: Acute discomfort at the cup site necessitating immediate removal.

    Skin Reactions: Includes local irritation, allergies, or burns. General Symptoms: Patients are screened for headache, nausea, and dizziness. All procedures are performed by licensed TCM physicians to ensure safety

Study contacts

Contact information is provided by the study sponsor or research team.

HUY HOANG LAM, Doctor

CONTACT

[email protected]

+ 84 933 - 887 - 373

Sponsors and collaborators

Lead sponsor

University of Medicine and Pharmacy at Ho Chi Minh City

Other

Registry information

Official study title

Effectiveness of Electroacupuncture Combined With Cupping Therapy in Patients With Shoulder Tendinitis and qi Stagnation and Blood Stasis Syndrome

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 22, 2026
Registry last updated
Apr 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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