Optimization of Lumbar Sensory Stimulation Parameters in Office Workers With Chronic Low Back Pain

NCT ID
NCT07801729
Registry status
Not yet recruiting
Study type
Not specified in the registry data
Phase
Not applicable
Sponsor
Mahidol University

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Enrollment: 36 participants (Estimated).

What is being studied

No interventions are listed in the registry data.

Who may be eligible

Ages
Not specified in the registry data
Sex
Not specified in the registry data
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: * Office workers who currently sit for at least 6 hours per workday. * Age 20-60 years. * Chronic nonspecific low back pain for at least 3 months. * Current pain intensity of at least 2/10 on the Numeric Pain Rating Scale. Exclusion Criteria: * History of seizure for either the subject or any family member * Implanted pacemaker * Contraindications for TMS and fNIRS, including open wound, infection, lesions, arteriosclerosis, history of hemophilia, or demand-type pacemaker * Acute cerebral hemorrhage * History of major spinal surgery, fracture, or traumatic injury to the lumbar spine. * Evidence of neurological deficits (e.g., radiculopathy, loss of sensation, or motor weakness in lower limbs). * Diagnosis of systemic inflammatory conditions (e.g., Ankylosing Spondylitis, Rheumatoid Arthritis). * Allergy to adhesives or history of severe skin sensitivity to vibration/mechanical pressure. * Body Mass Index (BMI) \> 30 kg/m2 (to ensure clarity of RUSI, dEMG, and fNIRs signal quality). * Pregnancy (due to changes in spinal biomechanics and hormones)

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Thailand

  • Changwat Nakhon Pathom, Thailand: 1

Sample of listed locations

  • Faculty of Physical Therapy, Mahidol University — Salaya, Changwat Nakhon Pathom, 73170, Thailand — Site recruitment status not specified in the registry data

Study details

Start date
January 1, 2027
Primary completion date
December 31, 2027
First posted
September 3, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07801729
Registry last updated
September 3, 2026
QualifiedStudies registry data refreshed
September 21, 2026

View NCT07801729 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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