- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06417255
Comparison Of The Effects Of Kinesiotape Application And Foam Roller Exercises
Comparison Of The Effects Of Kinesiotape Application And Foam Roller Exercises in Individuals With Chronic Low Back Pain
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Hazal GENÇ, PhD
- Phone Number: 05413204291
- Email: hazaloksuz@gmail.com
Study Locations
-
-
None Selected
-
Istanbul, None Selected, Turkey, 34353
- Recruiting
- Hazal GENÇ
-
Contact:
- Hazal GENÇ
- Phone Number: 05413204291
- Email: hazaloksuz@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients with chronic low back pain
- Individuals aged 18-60 years
- Patients without verbal communication barriers
- Patients without cognitive impairment (delirium, dementia, amnesia)
Exclusion Criteria:
- Exercise contraindication (uncontrolled medical conditions)
- Patients with previous spinal surgery
- Patients who develop an allergic reaction to the kinesiotape tape to be applied
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: kinesiotape application
|
The strips used for kinesiological taping can be applied by giving different shapes.
These shapes are I, Y, X, ring (donut), rake and net
|
Active Comparator: foam roller application
|
In the foam roller group, "Actifoam" brand non-serrated foam rollers with a size of "15x90" cm were used.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pressure Pain Measurement with Algometer
Time Frame: 6 weeks
|
The algometer, an effective way of measuring pressure pain threshold (PPT), is used to measure soft tissue pain associated with trigger points. Pittsburgh Sleep Quality Scale The Pittsburgh Sleep Quality Index is the most commonly used general measure in clinical and research settings to assess sleep quality and quantity. The Pittsburgh Sleep Quality Index (PSQI) consists of a total of 19 questions and 7 components to assess sleep quality during the last month. The total score had a value between 0-21 Schober Flexibility Test With the patient standing, the examiner marks the spinous process of the first sacral vertebra and 10 cm above this point. The patient is then asked to flex forwards as if trying to touch their toes while keeping their knees straight. If the distance between the two points does not increase by at least 5 cm, this is considered a sign of restriction in lumbar flexion. |
6 weeks
|
Pittsburgh Sleep Quality Scale
Time Frame: 6 weeks
|
The Pittsburgh Sleep Quality Index is the most commonly used general measure in clinical and research settings to assess sleep quality and quantity.
The Pittsburgh Sleep Quality Index (PSQI) consists of a total of 19 questions and 7 components to assess sleep quality during the last month.
The total score had a value between 0-21
|
6 weeks
|
Schober Flexibility Test
Time Frame: 6 weeks
|
With the patient standing, the examiner marks the spinous process of the first sacral vertebra and 10 cm above this point.
The patient is then asked to flex forwards as if trying to touch their toes while keeping their knees straight.
If the distance between the two points does not increase by at least 5 cm, this is considered a sign of restriction in lumbar flexion.
|
6 weeks
|
The finger-to-floor distance
Time Frame: 6 weeks
|
The finger-to-floor distance test is a test that measures specific physical disability.
This test is performed with the person standing upright with feet together.
The patient is asked to lean as far forward as possible with knees, arms and fingers fully extended.
The vertical distance between the tip of the middle finger and the floor is measured with a flexible tape measure.
|
6 weeks
|
Tampa Kinesiophobia Fatigue Scale
Time Frame: 6 weeks
|
The Tampa Kinesiophobia Scale measures fear of movement and fear of (re)injury during movement. High fear of movement and/or (re)injury, as measured by the Tampa Kinesiophobia Scale, has been found to be associated with poor performance on a number of physical tests. The minimum and maximum values of the Tampa Kinesiophobia Fatigue Scale are between 17 and 68. The total score range of this scale is between 0 and 68. |
6 weeks
|
Oswestry Scale
Time Frame: 6 weeks
|
The Oswestry Disability Index, first introduced by Fairbank et al. in 1980, is considered close to the gold standard for measuring the severity of disability due to low back pain. The Oswestry scale is a self-administered, free, easy-to-use and easy-to-score questionnaire containing 10 questions on different functional domains. The Oswestry Disability Index (ODI) is a widely used tool to assess disability related to low back pain. It consists of 10 sections addressing various daily activities, each scored on a scale of 0 to 5. The minimum score is 0, indicating no disability, while the maximum score is 50, indicating severe disability. |
6 weeks
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHRONIC LOW BACK PAIN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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