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Effectiveness of Kinesio Tapping for the Treatment of Patients With Acute Low Back Pain: A Randomized Control Trial

Effectiveness of Kinesio Tapping for the Treatment of Patients With Acute Low Back Pain: A Randomized Control Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05015842
Enrollment
56
Registered
2021-08-20
Start date
2019-01-02
Completion date
2019-06-03
Last updated
2021-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Keywords

Low back pain, Kinesio tapping, conventional physical therapy, Oswestry disability index

Brief summary

The objective of the study was to determine the effectiveness of Kinesio Taping (KT) for the treatment of patients with acute low back pain. In this study a total of 56 patients with acute low back pain were randomly allocated to the experimental group, KT along with conventional Physical therapy (PT), or the control group, conventional PT alone.

Detailed description

The objective of the study was to determine the effectiveness of Kinesio Taping (KT) for the treatment of patients with acute low back pain. In this study a total of 56 patients with acute low back pain were randomly allocated to the experimental group, KT along with conventional Physical therapy (PT), or the control group, conventional PT alone. 28 Patients received KT in addition to conventional PT while 28 patients received conventional PT alone for two weeks. Oswestry disability index (ODI) and numeric pain rating scale (NPRS) were used for the measurement of outcomes.

Interventions

OTHERConventional Physical Therapy

This is a combine protocol of different therapeutic exercises and heat therapy.

Kinesio Tapping is an adhesive and elastic fiber used for different outcomes like pain and swelling reduction among physical therapists.

Sponsors

NCS University System
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Both Genders * Age between 18 and 60 years * History of LBP less than

Exclusion criteria

* Patients having diagnosed conditions of spondylolisthesis, spondylosis, lumbar stenosis, spinal tumor, lumber fracture, renal disease and trauma were excluded from the study. * Patients either with chronic LBP (duration more than 3 months) or contraindicated to KT (skin allergy or pre-existing skin lesion or infection) were also excluded. * Female Pregnant patients were also excluded from the study.

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity2 weeksPain was measured on numerical pain rating scale. it is a scale with score from 0 to 10 where 0 is no pain and 10 is maximum pain. The minimum score mean better outcome while higher score mean worse outcome. simply lesser the score better would be the outcome.

Secondary

MeasureTime frameDescription
Functional Disability2 weeksFunctional disability was measured using Oswestry Disability Index (ODI. ODI score was converted to percentage so the score ranges from 0% to 100%. Where 0% mean no disability and 100 mean very severe (maximum) disability. The minimum score mean better outcome while higher score mean worse outcome. simply lesser the score better would be the outcome.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026