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OpenTrials
Completed

NCT Number: NCT04762563

Effect of Treatment on Connective Tissue in Low Back Pain

The purpose of the study is to investigate the effects of instrument assisted soft tissue mobilization (IASTM) and kinesiology taping (KT) that are additional treatment to the conservative treatment for the lumbar region and hamstrings and connective tissue thickness in patients with chronic non-specific low back pain (CNSLBP).

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Key information

Age range

30 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Emine Atıcı

Istanbul, None Selected, 34000, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • between the ages of 30 and 50
  • 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

  • the presence of allergy and skin diseases,
  • 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.

Treatment and study plan

IASTM application

Other

IASTM application .

Kinesio Tape® Tex Gold)

Other

Kinesio Tape® Tex Gold)

Primary outcomes

  1. straight leg test

    Time frame: 4 weeks

    Straight leg raise (SLR) was used to determine hamstring shortness. For SLR application, while the patient was lying on the back, the leg was lifted by the researcher to the level where the pain began, and the flexion angle in the hip was recorded

  2. sit and reach test

    Time frame: 4 weeks

    The sit and reach test (SRT) to measure the flexibility.During SRT application, the distance between the middle fingers of the hands and the feet was recorded while the patient was in the long sitting position in the bed and reached the toes with their hands without bending the knees

  3. Modified Schober test

    Time frame: 4 weeks

    Modified Schober Test and finger-ground distance evaluation for the spinal mobility assessment. For the Modified Schober Test, after marking 5 cm below and 10 cm above the spinous process of the lumbar vertebra while the patient was standing, the patient was asked to bend forward without bending the knees, and the change in the same range was recorded

  4. finger-ground distance measurement

    Time frame: 4 weeks

    While measuring "finger-ground distance", the patient was asked to touch the ground with both hands while standing with the knees in extension. The distance between the fingertip and the ground was recorded

  5. Ultrasonography

    Time frame: 4 weeks

    In this study, Siemens Acuson S 3000 device and Siemens HD 10 MHz linear probe were used for subcutaneous and perimuscular zone measurements.2 cm lateral to the midpoint of the L2-3 interspinous ligament is the area where the fascia planes are most parallel to the skin. In this study, the probe was centered at this point, which was determined while the patient was lying face down on the stretcher, and measurements were made from the right and left. For the measurement location in the hamstring region, the point where the fascia planes were most parallel to the skin was determined, as in the lumbar region. Measurement was performed in the area where the zones were most clearly seen lateral to the popliteal fossa.

Sponsors and collaborators

Lead sponsor

Okan University

Other

Collaborators

  • Medical Park Hospital Istanbul

Registry information

Official study title

The Effect of Instrument Assisted Soft Tissue Mobilization and Kinesiology Taping on Connective Tissue Thickness in Patients With Chronic Low Back Pain

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Feb 21, 2021
Registry last updated
Aug 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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