The Effect of TECAR Therapy on Pain Relief, Functional Disability and Range of Motion in Patients with Non-specific Chronic Low Back Pai

Not Applicable

Recruiting

• Conditions: on-specific chronic low back pain.; Low back pain

• Registration Number: IRCT20171224038043N1
• Lead Sponsor: niversity of social welfare and rehabilitation sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Men and women between the ages of 20 and 60
History of back pain for more than 3 months, or at least half a day in the last 6 months
Pain intensity greater than 3 according to V.A.S
Not having acute and inflammatory back pain, subacute and traumatic low back pain
Not having spinal canal stenosis, scoliosis and ankylosing spondylitis
Not having back pain after delivery or during pregnancy
Not having history of bone surgery, lumbar vertebral fracture, osteoporosis, infection, cancer, neurological diseases
Not having a history of any type of physical therapy for your back during the past month

Exclusion Criteria

Use of medication during research
Participant's reluctance to continue treatment
Doing exercises other than those trained in the course of treatment

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain severity score with the V.A.S index. Timepoint: The beginning and the end of each treatment session and one week after the completion of the study. Method of measurement: V.A.S index.;Functional disability assessment through Oswesterry and Roland-morris questionnaires. Timepoint: The beginning and the end of each treatment session and one week after the completion of the study. Method of measurement: Oswestry and Roland-morris questionnaires score.;Measuring the range of motion through the Inclinometer tilt. Timepoint: The beginning and the end of each treatment session and one week after the completion of the study. Method of measurement: Inclinometer Tilometer.