Effect of Treatment on Connective Tissue in Low Back Pain
NCT ID: NCT04762563
Last Updated: 2024-08-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
60 participants
INTERVENTIONAL
2021-03-01
2021-08-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
SINGLE
Study Groups
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Experimental: Study Group
Patients in the IASTM group were asked to lie face down on a stretcher, exposing the entire lumbar region. IASTM was applied to all paraspinal muscles for a total of 5 minutes after massage cream was applied. Immediately afterwards, the same application was performed for the right and left hamstring muscles from the gluteal line to the bottom of the popliteal fossa for 3 minutes after massage cream was applied. IASTM application was performed vertically, horizontally and diagonally using instruments of different sizes and shapes at an angle of 45 degrees to the skin surface.
IASTM application
IASTM application .
Active Comparator
KT application (Kinesio Tape® Tex Gold) was performed using the "muscle technique". In lumbar region application, while the patient was standing, the tape was cut as a Y-strip with a base of 5 cm.
Kinesio Tape® Tex Gold)
Kinesio Tape® Tex Gold)
Interventions
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IASTM application
IASTM application .
Kinesio Tape® Tex Gold)
Kinesio Tape® Tex Gold)
Eligibility Criteria
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Inclusion Criteria
* who had low back pain for at least 12 weeks,
* received no physical therapy in the last 6 months,
* received no IASTM or chemotherapy,
* had normal movement of the hip joint
* Visual Analog Scale value above 3
Exclusion Criteria
* pregnancy,
* major structural spinal deformity (scoliosis, kyphosis, stenosis),
* inflammatory disease,
* presence of extruded and sequestered herniation, -signs of neurological disease, -
* presence of orthopedic diseases such as fracture
* a history of spinal surgery.
30 Years
50 Years
ALL
No
Sponsors
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Medical Park Hospital Istanbul
OTHER
Okan University
OTHER
Responsible Party
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Emine Atıcı
Principal Investigator
Locations
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Emine Atıcı
Istanbul, None Selected, Turkey (Türkiye)
Countries
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Other Identifiers
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003
Identifier Type: -
Identifier Source: org_study_id
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