- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04173754
The Effectiveness of MSAT for Patients With ROM Limitation of the Shoulders
Observational Study on Effectiveness of MSAT(Motion Style Acupuncture Treatment) for Patients With ROM(Range of Motion) Limitation of the Shoulders Due to the Shoulder Diseases
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Motion Style Acupuncture Treatment(MSAT) is a therapeutic technique using acupuncture needle created in Jaseng Hospital. This treatment involves patients with musculoskeletal pain to move the part of their body actively during acupuncture treatment under physicians' observation. This treatment is known to relieve the pain and increase the range of motion(ROM). However, there has been no specific value for the effect of this treatment.
Therefore, The investigators conducted observational trial to analyze the effectiveness of shoulder MSAT. From July 2019, The investigators will collect 80 patients with ROM limitation on both or each shoulder and who are suffering from shoulder pain with the numeric rating scale(NRS) over 4.
The investigators will compare pain, dysfunction, quality of life and satisfaction of patients who are treated with Korean medical treatment including MSAT and patients who are treated with Korean medical treatment not including MSAT.
For these two groups, The investigators will compare Range Of Motion(ROM), NRS(Numeric Rating Scale), Visual Analogue Scale(VAS), Shoulder Pain and Disability Index(SPADI), Patient Global Impression of Change (PGIC) and EuroQol 5-Dimension (EQ-5D-5L).
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Busan, Korea, Republic of, 48102
- Haeundae Jaseng Hospital of Korean Medicine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with more than one ROM limitation(Abduction 180˚, Adduction 45˚, Flexion 180˚, Extension 45˚, Int. rot 80˚, Ext. rot 80˚) on both or each shoulder.
- Patients with NRS ≥ 4 for shoulder pain
- Patients aged 19-70 years on the date they sign the consent form.
- Patients who provide consent to participate in the trial and return the informed consent form
Exclusion Criteria:
- Patients who have been diagnosed with a severe disease that may cause ROM limitation of shoulder or shoulder pain,
- Patients with progressive neurological deficit or with serious neurological symptoms caused by spinal cord compression.
- Patients who visited a hospital in pain caused by a traffic accident.
- Patients with a severe mental illness.
- Patients who are difficult to complete the research participation agreement
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
MSAT Group
The MSAT group who are treated with korean medical treatment including MSAT will be evaluated on first, second, third visit and 2weeks after baseline. And the patients will receive telephone inquires after 3months from the baseline. The Korean medical treatment includes acupuncture, chuna, pharmaco-acupuncture and Korean herbal medicine. |
Motion Style Acupuncture Treatment(MSAT) is a therapeutic technique using acupuncture needle created in Jaseng Hospital.
This treatment involves patients with musculoskeletal pain to move the part of their body actively during acupuncture treatment under physicians' observation
|
|
Control Group
The control group who are treated with Korean medical treatment not including MSAT will be evaluated on first, second, third visit and 2weeks after baseline. And the patients will receive telephone inquires after 3months from the baseline. The Korean medical treatment includes acupuncture, chuna, pharmaco-acupuncture and Korean herbal medicine. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Shoulder mobility on the Shoulder ROM
Time Frame: At within 2 weeks
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Shoulder ROM was measured in six directions (Flexion, Extension, Abduction, Adduction, Right rotation, Left rotation) with goniometer.
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At within 2 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Rating Scale(NRS) of shoulder pain
Time Frame: At screening, baseline, 2 weeks, 3 months, and through study completion, an average of 3 month
|
The extent of shoulder pain and discomfort was assessed using NRS.
NRS is a pain scale in which the patient indicates their subjective pain as a whole number from 0 to 10.
The participant is asked to report their shoulder pain and discomfort using NRS, where 0 indicates 'no pain or discomfort' and 10 indicates 'the most severe pain and discomfort imaginable'.
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At screening, baseline, 2 weeks, 3 months, and through study completion, an average of 3 month
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Visual Analogue Scale (VAS) of shoulder pain
Time Frame: At screening, baseline, 2 weeks and through study completion, an average of 3 month
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VAS is an assessment index in which the patient records their pain on a 100mm line from 'no pain' at one end, and 'the most severe pain imaginable' at the other end.
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At screening, baseline, 2 weeks and through study completion, an average of 3 month
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|
Shoulder Pain and Disability Index(SPADI) questionnaire of shoulder pain and disability
Time Frame: At baseline, 2 weeks, 3 months
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SPADI is a self-administered questionnaire that consists of two dimensions, one for pain and the other for functional activities.
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At baseline, 2 weeks, 3 months
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Patient Global Impression of Change (PGIC)
Time Frame: At baseline, 2 weeks, 3 months
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The PGIC is an index that assesses improvements in functional limitation caused by whiplash injury.
Participants rate the improvement in functional limitations after treatment on a 7-point Likert scale (1=Very much improved, 4=No change, 7=Very much worse).
This index was originally developed for use in Psychology, but is currently used in various other medical fields to assess improvements in pain.
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At baseline, 2 weeks, 3 months
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EuroQol 5-Dimension (EQ-5D-5L)
Time Frame: At baseline, 2 weeks, 3 months
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The EQ-5D-5L is a method of indirectly calculating the weights of certain health states for quality of life after a multidimensional investigation of health states, and is the most widely used instrument for this purpose.
The EQ-5D consists of 5 questions about current health state (mobility, self-care, usual activities, pain, anxiety/depression), and each question is scored on a 5-point Likert scale (1=no problems, 3=moderate problems, 5=severe problems).
In this study, The investigators will use the Korean version of the EQ-5D-5L, which has been demonstrated to be valid.
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At baseline, 2 weeks, 3 months
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Adverse events(AE)
Time Frame: Through study completion, an average of 3 month
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Adverse events(AE) Physicians will monitor and record any unexpected or unintended patient reaction to integrative korean medicine at each visit.
Adverse events (AEs) associated with integrative korean medicine will include, but not be limited to, AEs anticipated from previous reports of korean medicine, and will stay open to all possibilities taking into consideration other potential, unknown AEs.
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Through study completion, an average of 3 month
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Shoulder mobility on the Shoulder ROM
Time Frame: At screening, baseline, 2 weeks, 3 months and through study completion, an average of 3 month
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Shoulder ROM was measured in six directions (Flexion, Extension, Abduction, Adduction, Right rotation, Left rotation) with goniometer.
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At screening, baseline, 2 weeks, 3 months and through study completion, an average of 3 month
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: In-Hyuk Ha, Jaseng Medical Foundation
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- JS-CT-2019-10
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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