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Active, not recruitingNCT07187336Updated Aug 5, 2026

The Efficacy and Safety of Shoulder Motion Style Acupuncture Treatment (MSAT) on in Patients With Shoulder Pain Caused by Traffic Accidents

An interventional study of Shoulder MSAT Group and Integrative Korean Medicine Only Group in Shoulder Pain, sponsored by Jaseng Medical Foundation. Active, not recruiting at 1 site in South Korea. Open to participants aged 19 Years to 70 Years. Per ClinicalTrials.gov, last updated 2026-08-05.

Sponsored by Jaseng Medical Foundation · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
98
Allocation
Randomized
Ages
19 Years to 70 Years
Sex
All
01

Study summary

This study will test the effectiveness and safety of Motion Style Acupuncture Treatment (MSAT) for shoulder pain caused by traffic accidents. About 98 hospitalized patients with acute shoulder pain after a traffic accident will take part.

Participants will be randomly assigned to one of two groups:

MSAT + integrative Korean medicine group (acupuncture, herbal medicine, pharmacopuncture, Chuna therapy, plus MSAT), or

Integrative Korean medicine only group (acupuncture, herbal medicine, pharmacopuncture, Chuna therapy).

MSAT involves inserting needles into the shoulder area and gently moving the joint to improve pain relief and mobility. All treatments used in this study are standard care in Korean medicine.

The main outcomes are pain reduction, shoulder movement, daily function, quality of life, and patient satisfaction. Safety will also be monitored by recording any side effects such as temporary soreness, bruising, or discomfort.

Treatment will be provided during hospitalization (up to 5 days), and patients will be followed up by phone at 2 weeks and 1 month after enrollment.

The results of this trial will help determine whether adding MSAT to standard integrative Korean medicine treatment provides greater benefit for patients with acute shoulder pain after traffic accidents.

Read the detailed description

This pragmatic randomized controlled trial is designed to evaluate the efficacy and safety of Motion Style Acupuncture Treatment (MSAT) for acute shoulder pain resulting from traffic accidents. Shoulder injuries after motor vehicle accidents often cause pain, restricted range of motion, and functional limitations. While integrative Korean medicine treatments such as acupuncture, pharmacopuncture, Chuna manual therapy, and herbal medicine are commonly used, there is limited high-quality evidence regarding the additional benefits of MSAT for shoulder conditions.

MSAT is a therapeutic technique in which acupuncture needles are inserted into affected areas while the practitioner guides or assists the patient's shoulder movements. This combined approach aims to enhance the analgesic and functional effects of acupuncture.

In this trial, 98 inpatients with acute shoulder pain following a traffic accident will be randomized equally into two groups. One group will receive integrative Korean medicine plus MSAT, and the other will receive integrative Korean medicine alone. MSAT will be performed once daily for three sessions during hospitalization (days 2-4), while both groups will continue standard integrative treatments.

The study will assess clinical effectiveness through changes in shoulder pain intensity, range of motion, functional status, quality of life, and patient global impression of change. Safety will be evaluated by monitoring adverse events during treatment and follow-up.

By comparing outcomes between the two groups, this study aims to provide evidence on whether MSAT offers additional benefit beyond integrative Korean medicine for patients with acute shoulder pain after traffic accidents. The findings are expected to contribute to establishing clinical guidance for safe and effective use of MSAT in real-world practice.

02

Conditions studied

  • Shoulder Pain

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Keywords

  • motion style acupuncture treatment
03

In context

Shoulder Pain

707 studies on the registry are indexed under Shoulder Pain; 152 are open to participants now.

This study's planned enrollment of 98 is above the median of 60 across 561 interventional studies indexed under Shoulder Pain.

Browse Shoulder Pain studies →

Lead sponsor

Jaseng Medical Foundation is the lead sponsor of 67 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
19 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

Adults aged 19 to 70 years

Hospitalized with shoulder pain within 5 days after a traffic accident

Shoulder pain intensity ≥ 5 on the Numeric Rating Scale (NRS) with observed limitation of movement

Able and willing to provide written informed consent

Exclusion criteria

Exclusion Criteria:

Serious conditions causing shoulder pain (e.g., malignant tumor, infection)

Progressive or severe neurological deficits

Recent shoulder surgery or procedure within 3 weeks

Shoulder pain mainly due to non-shoulder disorders (e.g., fibromyalgia, rheumatoid arthritis, gout)

Contraindications to MSAT (e.g., fracture, dislocation, ligament rupture or instability, severe inflammation)

Chronic diseases interfering with assessment (e.g., cardiovascular disease, renal disease, diabetic neuropathy, dementia, epilepsy)

Current use of steroids, immunosuppressants, psychiatric drugs, or other medications that may affect results

Contraindications to acupuncture (e.g., bleeding disorders, anticoagulant use, severe diabetes, severe cardiovascular disease)

Pregnant or planning pregnancy

Severe psychiatric illness

Participation in another interventional clinical trial

Unable to provide informed consent

Any other condition deemed inappropriate by the investigator

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
98 participants (estimated)

Study arms

  • Experimental
    Shoulder MSAT Group

    Participants receive integrative Korean medicine treatment plus Shoulder Motion Style Acupuncture Treatment (MSAT). MSAT: Acupuncture needles are inserted into the affected shoulder, and the practitioner guides or assists joint movements while the needles are retained. This aims to enhance pain relief and improve mobility. Treatment schedule: Once daily, 3 sessions during hospitalization (days 2-4). Additional integrative treatments: Acupuncture, pharmacopuncture, Chuna manual therapy, and herbal medicine, all provided as standard care.

    Procedure: Shoulder MSAT Group

  • Experimental
    Integrative Korean Medicine Only Group

    Participants receive integrative Korean medicine treatment only, without MSAT. Acupuncture: 6-10 points selected by the practitioner; 15-20 minutes per session. Pharmacopuncture: Injection of herbal extracts into acupuncture points. Chuna manual therapy: Manual therapy for 10-15 minutes daily. Herbal medicine: Decoction extracts packaged in pouches, taken twice daily after meals. Treatment schedule: Daily during hospitalization.

    Procedure: Integrative Korean Medicine Only Group

Interventions

  • ProcedureShoulder MSAT Group

    Shoulder Motion Style Acupuncture Treatment (MSAT) involves inserting acupuncture needles into specific points around the shoulder joint, then guiding or assisting the patient's shoulder movements while the needles remain in place. This combined technique is intended to maximize acupuncture effects by stimulating both the needles and the joint motion. In this study, MSAT will be performed once daily for three consecutive days (hospital days 2-4), in addition to standard integrative Korean medicine treatment (acupuncture, pharmacopuncture, Chuna manual therapy, and herbal medicine). Each MSAT session lasts about 10-20 minutes. This distinguishes the intervention from the comparator arm, which receives integrative Korean medicine treatment only, without MSAT.

  • ProcedureIntegrative Korean Medicine Only Group

    Participants in this group receive only standard integrative Korean medicine treatments, without MSAT. Treatments include acupuncture (6-10 points, 15-20 minutes per session), pharmacopuncture (injection of herbal extracts at acupuncture points), Chuna manual therapy (10-15 minutes daily), and herbal medicine (oral decoction extracts taken twice daily). This arm serves as the comparator to distinguish the additional effects of MSAT, since both groups receive the same integrative Korean medicine but only the experimental arm includes Shoulder MSAT.

06

What researchers measure

Primary outcomes

  1. Numeric Rating Scale for Shoulder Pain

    Patient-reported shoulder pain intensity measured using the Numeric Rating Scale, ranging from a minimum score of 0 (no pain) to a maximum score of 10 (worst imaginable pain). Higher scores indicate more severe pain and a worse outcome.

    Time frame: Baseline (Day 2, before treatment) to Day 5 (end of hospitalization).

Secondary outcomes

  1. Shoulder Range of Motion

    Active and passive shoulder range of motion measured in degrees using a goniometer in six directions: flexion (minimum 0°, maximum 180°), extension (0°-60°), abduction (0°-180°), adduction (0°-45°), internal rotation (0°-90°), and external rotation (0°-90°). Higher values indicate greater shoulder mobility and a better outcome.

    Time frame: Baseline, Day 5, 2 weeks, and 1 month after enrollment.

  2. Shoulder Pain and Disability Index

    The Shoulder Pain and Disability Index is a 13-item patient-reported questionnaire assessing shoulder pain (5 items) and disability (8 items). Each item is scored from a minimum of 0 to a maximum of 10. Subscale and total scores are calculated according to the instrument scoring guidelines, with higher scores indicating greater shoulder pain and disability and therefore a worse outcome.

    Time frame: Baseline, Day 5, 2 weeks, and 1 month after enrollment.

  3. EuroQol 5-Dimension 5-Level Questionnaire

    The EuroQol 5-Dimension 5-Level questionnaire is a standardized, patient-reported measure of health-related quality of life assessing five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension is rated on a 5-level scale. Responses are converted to an index value according to the country-specific value set, with higher index values indicating better health-related quality of life and a better outcome.

    Time frame: Baseline, Day 5, 2 weeks, and 1 month after enrollment.

  4. Patient Global Impression of Change

    The Patient Global Impression of Change is a patient-reported measure of overall change in condition since the start of the study, assessed on a 7-point scale ranging from 1 (very much improved) to 7 (very much worse). Lower scores indicate greater improvement and a better outcome.

    Time frame: Day 5, 2 weeks, and 1 month after enrollment.

  5. Adverse Events

    Any expected or unexpected adverse events assessed throughout the study, including but not limited to local pain, bruising, and systemic reactions, as reported by the patient and observed by the investigator. Adverse events are recorded by type, frequency, severity, and relationship to the intervention. Higher numbers of adverse events indicate worse safety outcomes.

    Time frame: During hospitalization, and at 2 weeks and 1 month follow-up.

07

Study locations

1 site
  • Haeundae Jaseng Hospital of Korean Medicine
    Busan, Haeundae 48102, South Korea
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07187336
Lead sponsor
Jaseng Medical Foundation
Responsible party
Sponsor
First posted
Sep 23, 2025
Start date
Nov 2, 2025
Primary completion
Feb 25, 2026
Completion
Aug 30, 2026 (estimated)
Last update
Aug 5, 2026

Study contacts

In-Hyuk Ha, phD
principal investigator · Jaseng Medical Foundation

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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