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The Comparison of Effectiveness of Electroacupuncture and Sham Electroacupuncture Among Chronic Low Back Pain Patients: A Randomized Controlled Trial

The Comparison of Effectiveness of Electroacupuncture and Sham Electroacupuncture Among Chronic Low Back Pain Patients: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260219010
Enrollment
40
Registered
2026-02-19
Start date
2025-10-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Participants diagnosed with chronic low back pain (CLBP), defined as pain persisting for at least 3 months. Chronic Low Back Pain, Electroacupuncture, Sham Electroacupuncture

Interventions

Participants in the Electroacupuncture group received acupuncture at acupoints BL20, BL21, BL23, and BL25. Following needle insertion, electrode clips were attached to the needle handles at these poin
Experimental Other,Sham Comparator Other
Electroacupuncture Group (EA Group),Sham Electroacupuncture Group (Sham EA Group)

Sponsors

Personal Funding
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Male and female participants aged 25 to 60 years 2.Diagnosed with CLBP for at least 3 months 3.Baseline pain score of 1 to 6 (mild to moderate) on the Numerical Rating Scale (NRS) 4.Normal skin sensation in the treatment area, verified by a light touch test

Exclusion criteria

Exclusion criteria: 1.Signs of spinal cord or nerve root compression presenting with progressive neurological deficits (e.g., muscle weakness), confirmed by medical evaluation. 2.Conditions impairing sensory or motor function that may confound pain assessment (e.g., stroke, traumatic brain injury). 3.Presence of a cardiac pacemaker or intracardiac defibrillator (ICD), due to safety risks associated with electroacupuncture. 4.Pain accompanied by severe restriction of mobility or bedridden status. 5.History of spinal or back surgery within the preceding 6 months. 6.Presence of contraindications or risks associated with acupuncture and electroacupuncture, including: known or suspected malignancy; severe infection or immunodeficiency; coagulation disorders or bleeding diathesis; skin infection at the needle insertion sites; metal implants within the treatment area; history of seizures; severe hypertension (systolic blood pressure > 180 mmHg); or pregnancy

Design outcomes

Primary

MeasureTime frame
Pain Intensity Assessment Immediately before and after treatment sessions 1, 2, 3, 4, and 5 (Total of 10 assessment time points) Numerical Rating Scale (NRS),Thai Version of the Oswestry Disability Index (ODI) Immediately after treatment sessions 1, 2, 3, 4, and 5 Self-administered questionnaire

Secondary

MeasureTime frame
General Information Questionnaire Baseline (prior to the first treatment session) Questionnaire,The Global Perceived Effect Scale (GPE) Immediately after treatment sessions 2, 3, 4, and 5 Self-Report Questionnaire,Satisfaction Immediately after treatment sessions 1, 2, 3, 4, and 5 Self Questionnaire

Countries

Thailand

Contacts

Public ContactKanthon Pattarapornpairot

1. School of Anti-Aging and Regenerative Medicine, Mae Fah Luang University and 2. Traditional Chinese Medicine Clinic, Thai Traditional and Alternative Medicine Center, Department of Thai Traditional and Alternative Medicine

kanthonp.pairot@gmail.com0814164097

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026