UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000061391
Receipt number R000070241
Scientific Title Effects of Moxibustion on chronic neck and shoulder pain and Postural Control in Workers with Katakori
Date of disclosure of the study information 2026/04/27
Last modified on 2026/04/27 16:51:30

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Basic information

Public title

Effects of Moxibustion on chronic neck and shoulder pain (katakori) and Postural Control

Acronym

Effects of Moxibustion on chronic neck and shoulder pain (katakori) and Balance

Scientific Title

Effects of Moxibustion on chronic neck and shoulder pain and Postural Control in Workers with Katakori

Scientific Title:Acronym

Effects of Moxibustion on chronic neck and shoulder pain (katakori)

Region

Japan


Condition

Condition

chronic neck and shoulder pain (katakori)

Classification by specialty

Not applicable

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aim of this study is to investigate whether moxibustion can be a useful intervention for workers with chronic neck and shoulder pain (katakori).

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

numerical rating scale

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Cross-over

Randomization

Randomized

Randomization unit

Individual

Blinding

Open -but assessor(s) are blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

Moxibustion

Interventions/Control_2

No treatment

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

18 years-old <=

Age-upper limit

65 years-old >

Gender

Male and Female

Key inclusion criteria

1. Individuals in whom no apparent organic disease is identified on health examination.
2. Individuals with moderate chronic neck and shoulder pain (katakori), defined as a Numerical Rating Scale (NRS) score of 4/10 or higher, persisting for at least 3 months.
3. Individuals with no abnormal neurological findings in the upper extremities, including deep tendon reflexes, muscle strength, and sensory testing.

Key exclusion criteria

1. Individuals with abnormalities of the vestibular or visual system.
2. Individuals with a history of spinal surgery.
3. Individuals with rheumatic diseases.
4. Individuals with diseases affecting the spine.
5. Individuals with any other disease or injury affecting the cervical region.
6. Pregnant individuals.
7. Individuals currently participating in another clinical trial or investigational study.
8. Individuals with a history of allergic reactions to pharmaceuticals or cosmetics (e.g., rash, redness, itching, or dermatitis).
9. Individuals with fragile or sensitive skin (e.g., diseased, sensitive, or unstable skin).
10. Individuals with a mugwort allergy.
11. Individuals who are sensitive to smoke or odors.
12. Individuals judged by the investigator to be unsuitable for participation in the study.

Target sample size

34


Research contact person

Name of lead principal investigator

1st name Yoichi
Middle name
Last name Minakawa

Organization

Teikyo Heisei University

Division name

Faculty of Health Care

Zip code

1708445

Address

2-51-4 Higashiikebukuro, Toshima-ku, Tokyo

TEL

03-5843-3111

Email

y.minakawa@thu.ac.jp


Public contact

Name of contact person

1st name Yoichi
Middle name
Last name Minakawa

Organization

Teikyo Heisei University

Division name

Faculty of Health Care

Zip code

1708445

Address

2-51-4 Higashiikebukuro, Toshima-ku, Tokyo

TEL

03-5843-3111

Homepage URL


Email

y.minakawa@thu.ac.jp


Sponsor or person

Institute

Teikyo Heisei University

Institute

Department

Personal name



Funding Source

Organization

Teikyo Heisei University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Teikyo Heisei University Ethical Committee

Address

2-51-4 Higashiikebukuro, Toshima-ku, Tokyo

Tel

0358433111

Email

rec@thu.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions

帝京平成大学


Other administrative information

Date of disclosure of the study information

2026 Year 04 Month 27 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Open public recruiting

Date of protocol fixation

2026 Year 03 Month 19 Day

Date of IRB

2026 Year 03 Month 19 Day

Anticipated trial start date

2026 Year 04 Month 27 Day

Last follow-up date

2027 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2026 Year 04 Month 27 Day

Last modified on

2026 Year 04 Month 27 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000070241