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The effect of cognitive behavioral therapy (CBT) programs with cathodal DLPFC transcranial direct current stimulation on fear in patient with non-specific chronic low back pain with high fear

The effect of cognitive behavioral therapy (CBT) programs with cathodal DLPFC transcranial direct current stimulation on fear in patient with non-specific chronic low back pain with high fear

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150302021294N6
Enrollment
45
Registered
2018-02-07
Start date
2017-12-22
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Low back pain. Low back pain

Interventions

Intervention 1: Intervention group 1: Cognitive behavioral therapy with 20 minutes cathodal transcranial direct current stimulation on left DLPFC for 4 weeks, 2 sessions in each week. Intervention 2:

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Age between 18-45 Having periodic low back pain for 12 weeks Visual analog scale less than 3 Pain anxiety symptoms scale more than 30

Exclusion criteria

Exclusion criteria: Any symptoms of spinal cord involvement Cauda equina syndrome symptoms Sciatica symptoms Root canal involvement symptoms History of spinal surgery Fracture in spinal column Impairment of learning Pregnancy

Design outcomes

Primary

MeasureTime frame
Score of fear in Pain Anxiety Symptoms Scale. Timepoint: Before interventions, immediately after intervention and 2 weeks after intervention. Method of measurement: Pain Anxiety Symptoms Scale to measure fear of pain.;Score of fear of movement in Tampa Scale for Kinesiophobia. Timepoint: Before intervention, immediately after intervention and 2 weeks later after intervention. Method of measurement: Tampa Scale for Kinesiophobia to measure fear of movement.;Disability. Timepoint: Before intervention, immediately after intervention and 2 weeks later after intervention. Method of measurement: Roland Morris questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Ehsani

Semnan University of Medical Sciences

fatemehehsani@gmail.com+98 33654180

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026