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NCT05713812 Clinical Trial

"EFFECTS OF KINESIO-TAPING ON PAIN, POSTURAL STABILITY AND FUNCTION IN PERSONS WITH DISCOGENIC LOW BACK PAIN"

Low Back Pain Clinical Trial

Official title:
"EFFECTS OF KINESIO-TAPING ON PAIN, POSTURAL STABILITY AND FUNCTION IN PERSONS WITH DISCOGENIC LOW BACK PAIN"

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT05713812
Other study ID # FUI/CTR/2023/4
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date February 15, 2023
Est. completion date August 30, 2023

Study information
Verified date January 2023
Source Foundation University Islamabad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Low back pain is the leading cause of disability worldwide, the prevalence of low back pain can be as high as 43%. Past research has shown the positive effects of Kinesio taping in patients with chronic and nonspecific low back pain in pain reduction, improvement in postural stability, and improvement in function. However, no study has yet evaluated the effects of KT in persons with discogenic LBP. If found to be effective KT can be prescribed as a conservative & cost-effective treatment for patients with discogenic low back pain.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 36
Est. completion date August 30, 2023
Est. primary completion date August 15, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 45 Years
Eligibility Inclusion Criteria: - Age20-45 years. - Positive straight leg raise (SLR) - Posterolateral disc bulge, herniation or prolapse indicated by MRI. - Positive centralization and peripheralization phenomenon. Exclusion Criteria: - Participants having spondylolisthesis, fractures, tumors, osteoporosis, infection, or spinal stenosis. - History of lumbar spine surgery and patients that are already receiving any physical therapy or exercise - Skin allergy or sensitivity to the tape. - Neurological, rheumatologic, or psychiatric disease

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Kinesiotaping
Kinesiotape will be applied
• Control Treatment
IFC + Hot pack for 20 minutes MDT (prone positioning) for 10 minutes. Lumbar SNAGs + lumbar rotation mobilization. Home exercise plan: MDT for 10 min + patient education to avoid flexion based activities.

Locations
Country Name City State
Pakistan Foundation University Islamabad Islamabad Federal

Sponsors (1)
Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Back Pain Back Pain will be measured via numerical pain rating scale. A higher score signifies greater pain. 2 weeks.
Primary Postural Stability Postural Stability will be measured via Biodex Balance System. A higher score signifies poorer stability. 2 weeks.
Primary Disability Disability will be measured via Oswestry Disability Index. A higher score signifies poorer outcome. 2 weeks.
Primary Gait velocity velocity of gait will be measured via gait analysis. 2 weeks.
Primary Stride length Stride length of gait will be measured via gait analysis. 2 weeks.
Primary Cadence Cadence of gait will be measured via gait analysis. 2 weeks.
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