UMIN-ICDS Clinical Trial
| Unique ID issued by UMIN | UMIN000062066 |
|---|---|
| Receipt number | R000071020 |
| Scientific Title | Effects of Acupuncture Stimulation at Active Trigger Points and Non-Trigger Point Sites on Quantitative Sensory Testing in Patients with Chronic Low Back Pain: A Randomized Controlled Trial |
| Date of disclosure of the study information | 2026/06/27 |
| Last modified on | 2026/06/26 13:38:57 |
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Basic information
Public title
Comparison of the Effects of Different Acupuncture Sites on Pain in People with Chronic Low Back Pain
Acronym
CLBP Acupuncture Site Study
Scientific Title
Effects of Acupuncture Stimulation at Active Trigger Points and Non-Trigger Point Sites on Quantitative Sensory Testing in Patients with Chronic Low Back Pain: A Randomized Controlled Trial
Scientific Title:Acronym
The Effect of TrP Acupuncture Stimulation on Quantitative Sensory Testing in Patients with Chronic Low Back Pain
Region
| Japan |
Condition
Condition
Chronic Low Back Pain
Classification by specialty
| Orthopedics |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to compare the effects of acupuncture stimulation at active trigger points and non-trigger point sites on quantitative sensory testing (pressure pain threshold and temporal summation) and pain intensity in patients with chronic low back pain, thereby clarifying the characteristics of the analgesic effects of trigger point acupuncture.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Changes in quantitative sensory testing outcomes, including pressure pain threshold (PPT) and temporal summation (TS), from baseline to immediately after the intervention.
Key secondary outcomes
Change in pain intensity measured using the Visual Analog Scale (VAS) from baseline to immediately after the intervention.
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -no one is blinded
Control
Active
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Maneuver |
Interventions/Control_1
Under ultrasound guidance, a disposable stainless steel needle is inserted into the tissue within the lumbar multifidus where reproduction of the participant's usual low back pain was confirmed during the pre-assessment, and retained for 15 minutes.
Interventions/Control_2
nder ultrasound guidance, a disposable stainless-steel needle is inserted 10 mm shallower than the tissue where pain reproduction was identified during the pre-assessment, with the absence of symptom reproduction confirmed, and retained for 15 minutes.
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
Adults aged 18~65 years.
Students or employees of the university.
Individuals with chronic low back pain lasting for at least 3 months.
No history of lumbar spine surgery.
No symptoms suggestive of lower extremity radiculopathy.
Reproduction of their usual low back pain upon manual compression of the lumbar multifidus muscle, including the area approximately 2 cm lateral to the midline at the L4 vertebral level.
Ability to reliably report symptom reproduction during acupuncture stimulation.
Previous experience with acupuncture treatment.
Provision of written informed consent.
Key exclusion criteria
Individuals with severe fear of acupuncture treatment.
Individuals who have previously experienced all acupuncture stimulation as strongly unpleasant or painful sensations.
Pregnant women or individuals who may be pregnant.
Individuals with bleeding disorders or those receiving anticoagulant therapy.
Individuals with severe orthopedic, neurological, or psychiatric disorders.
Individuals deemed unsuitable for study participation by the principal investigator.
Target sample size
20
Research contact person
Name of lead principal investigator
| 1st name | yoji |
| Middle name | |
| Last name | kitagawa |
Organization
Kansai University of Health Sciences
Division name
Faculty of Health Sciences
Zip code
5900482
Address
2-11-1 Wakaba, Kumatori-cho, Sennan-gun, Osaka 590-0482, Japan
TEL
0724538251
kitagawa@kansai.ac.jp
Public contact
Name of contact person
| 1st name | yoji |
| Middle name | |
| Last name | kitagawa |
Organization
Kansai University of Health Sciences
Division name
Faculty of Health Sciences
Zip code
5900482
Address
2-11-1 Wakaba, Kumatori-cho, Sennan-gun, Osaka 590-0482, Japan
TEL
0724538251
Homepage URL
kitagawa@kansai.ac.jp
Sponsor or person
Institute
Kansai University of Health Sciences
Institute
Department
Personal name
Funding Source
Organization
Kansai University of Health Sciences
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
Kansai University of Health Sciences
Address
2-11-1 Wakaba, Kumatori-cho, Sennan-gun, Osaka 590-0482, Japan
Tel
0724538251
kitagawa@kansai.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
Other administrative information
Date of disclosure of the study information
| 2026 | Year | 06 | Month | 27 | Day |
Related information
URL releasing protocol
Publication of results
Partially published
Result
URL related to results and publications
Number of participants that the trial has enrolled
20
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
Completed
Date of protocol fixation
| 2020 | Year | 10 | Month | 21 | Day |
Date of IRB
| 2020 | Year | 10 | Month | 21 | Day |
Anticipated trial start date
| 2020 | Year | 10 | Month | 21 | Day |
Last follow-up date
| 2025 | Year | 09 | Month | 26 | 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 | 06 | Month | 26 | Day |
Last modified on
| 2026 | Year | 06 | Month | 26 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000071020
