Chronic Low-back Pain Clinical Trial
Official title:
Acute and Chronic Effects of High Frequency RF Electrical Current on Pain and Muscle Function in Individuals With Musculoskeletal Pain
The purpose of this study is to examine the acute and chronic effects of high frequency electrical current transfer (frequently called "TECAR") on pain and functional movement in individuals with a musculoskeletal injury or pain. The participants will be assigned into an experimental or a control group and outcome measures will be measured prior to, after, 24 and 48 hours following a single intervention session (Acute effects) as well as 3 and 6 months after the intervention (chronic effects).
Status | Recruiting |
Enrollment | 50 |
Est. completion date | December 31, 2024 |
Est. primary completion date | May 31, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Muscle injury group Inclusion Criteria: - Acute hamstring or quadriceps or calf strain injury - Age above 18 years Exclusion Criteria: - Other injury or musculoskeletal condition - Any observed organ dysfunctions - Receipt of medication or treatment for the past 3 months Low back pain group Inclusion criteria - Pain between bottom of ribs and buttock creases - Incidents for at least half the days in the past six months - Visual analogue pain score equal or greater than 2/10 Exclusion Criteria: - spinal stenosis - radiographic evidence of inflammatory disease affecting the spine - fracture - spondylolysis or spondylolisthesis - important genetic structure abnormality in the spine - daily intensive low back pain - pregnancy - use of medication that might influence heart rate and/or blood pressure - psychiatric disorders - receipt of medication or treatment for the past 3 months |
Country | Name | City | State |
---|---|---|---|
Greece | Physiotherapy Clinic | Kavala | |
Greece | Laboratory of Neuromechanics, Department of Physical Education and Sport Science, Aristotle University of Thessaloniki | Serres |
Lead Sponsor | Collaborator |
---|---|
Aristotle University Of Thessaloniki |
Greece,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in pain Intensity | Visual analogue scale. Scale ranges from 0 to 10. 0 indicates no pain and 10 maximum intensity pain | Day before, day 0, day 1, day 2, month 3, month 6 | |
Primary | Change in sit and reach test measurement | From supine position, with the feet in contact with a wooden box and the trunk flexed, participants attempt to reach with their hands as far as posible. Score is measured in cm. A higher measurement indicates higher flexibility | Day before, day 0, day 1, day 2, month 3, month 6 | |
Primary | Change in straight leg raising test | From supine position, the tester raises one leg (with the knee flexed about 10-20 degrees) until discomfort is reported. The range of motion (in degrees) is stored. | Day before, day 0, day 1, day 2, month 3, month 6 | |
Primary | Change in prone flexibility test | From the prone position, the tester flexes the knee of the participant. The maximum range of motion is stored in degrees | Day before, day 0, day 1, day 2, month 3, month 6 | |
Primary | Change in Oswestry index score | A questionnaire which provides a score which reflects function in activities of daily living for those with acute or chronic back pain. It consists of 10 categories of questions, with a total sum of 50. Score is expressed as a percentage of 50, where 0% indicates no functional disability and pain. 100% indicates maximum functional disability and pain | Day before, day 0, day 1, day 2, month 3, month 6 | |
Secondary | Change in single leg balance test center of pressure | Displacement of center of pressure during a 30s single-leg standing test on a pressure platform. A greater center of pressure displacement indicates less postural stability. | Day before, day 0, day 1, day 2, month 3, month 6 |
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