Immediate Effects of Kinesio Taping on Pain and Postural Stability in Persons With Discogenic Low Back Pain.

Sponsor
Foundation University Islamabad (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05542186
Collaborator
(none)
40
1
1
7
5.7

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Kinesiotaping
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Immediate Effects of Kinesio Taping on Pain and Postural Stability in Persons With Discogenic Low Back Pain.
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Feb 1, 2023
Anticipated Study Completion Date :
Apr 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Kinesiotaping

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

Outcome Measures

Primary Outcome Measures

  1. Pain Pressure Threshold [1 day]

    Pain Pressure Threshold will be measured using algometer before and after the treatment session. Higher score signifies positive outcome.

  2. Back Pain [1 day]

    Pain will be measured using numeric pain rating scale before and after the treatment session. Higher score signifies negative outcome.

  3. Postural Stability [1 day]

    Postural Stability will be measured using Biodex Balance System before and after the treatment session

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Foundation University Islamabad Pakistan

Sponsors and Collaborators

  • Foundation University Islamabad

Investigators

  • Principal Investigator: Bisma Mazhar, MS, FUI
  • Study Chair: Muhammad Osama, PhD*, FUI

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Foundation University Islamabad
ClinicalTrials.gov Identifier:
NCT05542186
Other Study ID Numbers:
  • FUI/CTR/2022/11
First Posted:
Sep 15, 2022
Last Update Posted:
Sep 15, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 15, 2022