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Effect of IFC combined US in low back pain

Effects of interferential current combined with pulse ultrasound in individuals with chronic non-specific low back pain

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250512005
Enrollment
36
Registered
2025-05-12
Start date
2025-07-25
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

Non-specific low back pain (NSLBP) is a prevalent condition affecting up to 84% of the adult population, frequently progressing to chronicity and diminishing quality of life. Interferential current (IFC) therapy has demonstrated effectiveness in alleviating musculoskeletal pain using 2KHz and 4KHz carrier frequencies, though conventional treatment protocols require sessions of 30 minutes or longer. The integration of IFC with ultrasound technology enables deeper tissue penetration and significan

Interventions

IFC setting: Carrier frequency 2 KHz, AMF 100 Hz with intensity at strong sensation without pain, combined with US frequency 1 MHz in pulse mode with frequency 48 Hz, duty cycle 20%, intensity 1.20 W/
Experimental Other,Active Comparator Other
Group A: IFC2KHz/100Hz with pulse US,Group B: IFC4KHz/100Hz with pulse US

Sponsors

Faculty of Associated Medical Sciences, Khon Kaen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Male or female, 2. Age between 18 40 years, 3 Has chronic low back pain of nonspecific cause for more than 12 weeks, 4 Has pain in the lower back area which may or may not be accompanied by radiating pain down the leg, 5 Body mass index is within normal range, with BMI between 18.50-24.99 kg per meter square -Has pain level when assessed with numeric rating scale scoring between 4 to 7 points

Exclusion criteria

Exclusion criteria: 1. Has been diagnosed with disc herniation, 2. Has abnormal skin sensation such as numbness or feeling of pins and needles, 3. Has no lower back pain on the day of assessment before beginning the study. 4, Has used pain medication, anti-inflammatory drugs, or muscle relaxants within 24 hours before treatment, 5. Has a history of bone fracture and/or previous surgery in the spine or leg area, 6. Has been diagnosed with specific causes of lower back pain including: infection, metastasis, osteoporosis, rheumatoid arthritis, 7. Has cauda equina syndrome (inability to control urination or defecation, or incomplete urination or defecation), 8. Female who is pregnant or breastfeeding, 9. Has contraindications for electrical and ultrasound therapy including: metal implants in the spine and/or thigh, use of pacemaker, skin disease in the back area, open wound in the back area, impaired communication, deep vein thrombosis or thrombophlebitis, malignancy, radiation therapy within the past 3 months, infection, impaired circulation, or tuberculosis, 10. Has neuromuscular disease such as fibromyalgia, spinal muscular atrophy (SMA), etc., 11. Is currently receiving treatment for chronic lower back pain of unclear cause, 12. Has a history of brain and/or spinal cord injury

Design outcomes

Primary

MeasureTime frame
Pain intensity at baseline, immediately after 1st treatment, post-treatment, and one-month follow-up periods Numeric rating scale (NRS)

Secondary

MeasureTime frame
Lumbar ROM at baseline, immediately after 1st treatment, post-treatment, and one-month follow-up periods Modified Modified Schober's test (MMST) using tape measurement in cm.,Joint position sense at baseline, immediately after 1st treatment, post-treatment, and one-month follow-up periods Joint position sense error (distance of error in cm.)),Self-rated functional disability at baseline, post-treatment, and one-month follow-up periods Oswestry disability questionnaires (score) which is rated by participants,Self-rated functional disability at baseline, post-treatment, and one-month follow-up periods Roland Morris Disability Questionnaire which is rated by participants

Countries

Thailand

Contacts

Public ContactTorkamol Hunsawong

Faculty of Associated Medical Sciences, Khon Kaen University

tkmhun@kku.ac.th0927861984

Outcome results

None listed

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