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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05542186
Other study ID # FUI/CTR/2022/11
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date September 2022
Est. completion date April 2023

Study information

Verified date September 2022
Source Foundation University Islamabad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Discogenic LBP is the leading cause of disability worldwide. Eventhough other types of Chronic LBP are more common, 63% of all patients reporting to tertiary care hospital with LBP are discogenic in nature. However, immediate effects of kinesio-taping on pain and postural stability in discogenic low back pain has not been well documented in existing literature. This study is focused on immediate effects of kinesiotaping on pain and postural stability in persons with discogenic low back pain.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 40
Est. completion date April 2023
Est. primary completion date February 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria: - Participants in an age range of 20-65 years will be considered for this study. - Participants with disc bulge, herniation or prolapse indicate by MRI. - Positive straight leg raise (SLR) Positive centralization and peripheralization phenomenon. - Participants with MRI findings conclusive of disc pathology will be included. Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Kinesiotaping
Biomechanical correction for discogenic low back pain using kinesiotaping

Locations

Country Name City State
Pakistan Foundation University Islamabad

Sponsors (1)

Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Pressure Threshold Pain Pressure Threshold will be measured using algometer before and after the treatment session. Higher score signifies positive outcome. 1 day
Primary Back Pain Pain will be measured using numeric pain rating scale before and after the treatment session. Higher score signifies negative outcome. 1 day
Primary Postural Stability Postural Stability will be measured using Biodex Balance System before and after the treatment session 1 day
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