Low Back Pain Clinical Trial
Official title:
Evaluation of the Kinesiology Taping Effectiveness in the Treatment of Lumbar Spine Pain in Subjects Under 30 Years of Age
Verified date | October 2021 |
Source | John Paul II University of Applied Sciences in Biala Podlaska |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Lumbar spine pain syndromes are one of the most common pain conditions in our society. The purpose of kinesiotaping is to normalize muscle function, improve blood and lymph flow, reduce pain, improve proprioception, promote tissue healing and restore normal tissue function. Today, this method is used in many fields of medicine. Its primary purpose is to support the musculoskeletal system by using various types of applications. There is a lack of publications in the global literature on the effect of kinesiotaping of the external oblique muscles on lumbar spine pain. The main objective of this study is to evaluate the effectiveness of kinesiology taping in the treatment of lumbar spine pain in individuals under 30 years of age.
Status | Completed |
Enrollment | 80 |
Est. completion date | March 30, 2022 |
Est. primary completion date | March 29, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 30 Years |
Eligibility | Inclusion Criteria: - participants' age between 18 and 30, - the presence of pain in the lumbar region of the spine, - participants who have not been using non-steroidal anti-inflammatory drugs (NSAIDs) for at least one week prior to study entry, - no contraindications to the use of dynamic kinesiology taping patches, - informed, written consent to participate in the study. Exclusion Criteria: - status of the post lumbar spine surgery, - subjects who have had a spinal injury within 6 months prior to the start of the study, - neoplastic diseases, - congenital structural pathologies of the spine, - allergy to the adhesive substance of kinesiology taping or paper patch, - being a physiotherapy student. |
Country | Name | City | State |
---|---|---|---|
Poland | Laboratory of Pope John Paul II State School Of Higher Education in Biala Podlaska | Biala Podlaska | |
Poland | Pope John Paul II State School Of Higher Education in Biala Podlaska | Biala Podlaska |
Lead Sponsor | Collaborator |
---|---|
John Paul II University of Applied Sciences in Biala Podlaska |
Poland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual analogue scale of pain (VAS) | Visual analogue scale of pain (VAS) evaluates intensity of pain in the scale from 0 to 10. Maximum score means the highest level of pain. | Visual analogue pain scale (VAS) will be carried out before the start of the therapy. | |
Primary | Visual analogue scale of pain (VAS) | Visual analogue scale of pain (VAS) evaluates intensity of pain in the scale from 0 to 10. Maximum score means the highest level of pain. | Visual analogue pain scale (VAS) will be carried out 4 days of therapy, immediately after its completion. | |
Primary | Visual analogue scale of pain (VAS) | Visual analogue scale of pain (VAS) evaluates intensity of pain in the scale from 0 to 10. Maximum score means the highest level of pain. | Visual analogue pain scale (VAS) will be carried out four weeks after the end of the treatment. | |
Secondary | Modified Laitinen's pain questionnaire | The Laitinen questionnaire takes into account four indicators evaluated in a scale of 0 to 4: the intensity of pain, the frequency of its occurrence, the use of analgesic medications and limitation of the participant's motor activity. A research participant could be granted from 0 to 16 points, the maximum score meaning the highest level of pain. | Modified Laitinen's pain questionnaire will be carried out three times (before the start of the therapy, after 4 days of therapy, immediately after its completion and four weeks after the end of the treatment | |
Secondary | Oswestry Disability Index | Oswestry Disability Index takes into account ten indicators evaluated in a scale of 0 to 5. A research participant could be granted from 0 to 50 points, the minimum score meaning the highest level of disability. | Oswestry Disability Index will be carried out three times (before the start of the therapy, after 4 days of therapy, immediately after its completion and four weeks after the end of the treatment |
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