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Effectiveness of the Addition of the Kinesio Taping Method to Conventional Physical Therapy Treatment in Patients With Chronic Nonspecific Low Back Pain

Effectiveness of the Addition of the Kinesio Taping Method to Conventional Physical Therapy Treatment in Patients With Chronic Nonspecific Low Back Pain: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01866332
Enrollment
148
Registered
2013-05-31
Start date
2013-06-30
Completion date
2014-12-31
Last updated
2015-01-15

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

Conditions

Nonspecific Chronic Low Back Pain

Keywords

back pain, tape, chronic

Brief summary

The purpose of this study is to determine the effectiveness of the addition of the use of Kinesio Taping in patients with chronic nonspecific low back pain who receive conventional physical therapy.

Detailed description

One hundred and forty-eight patients will be randomized to receive either conventional physical therapy, which consist of a combination of manual therapy techniques, general exercises and specific exercises for spinal segmental stabilization (Conventional Physical Therapy Group) or to receive conventional physical therapy plus the addition of the Kinesio Taping in the lumbar spine (Conventional Physical Therapy plus Kinesio Taping), over a period of 5 weeks (10 sessions of treatment). Clinical outcomes (pain intensity, disability and global perceived effect ) will be collected at baseline and at 5 weeks, 3 and 6 months after randomization. Data will be collected by a blinded examiner who will be unaware about the group allocation. All statistical analysis will be conducted following the principles of intention to treat analysis and the between-group differences will be performed using Mixed Linear Models.

Interventions

OTHERConventional Physical Therapy

Combination of manual therapy techniques, general exercises and specific exercises for spinal segmental stabilization. Patients will receive 10 sessions of treatment over a period of five weeks (two sessions/week). The treatment will be tailored to the patient presentation (i.e. pragmatic treatment).

DEVICEKinesio Tex Gold ( Kinesiotaping )

Kinesiotaping intervention is based upon the use of specific elastic tapes (known as Kinesio Tex Gold) that are applied with a certain amount of tension fixed to the skin of patients with the target muscles in a stretched position. The tapes will be placed over the superficial back muscles (erector spinae muscles).

Sponsors

Universidade Cidade de Sao Paulo
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Patients with non-specific low back pain longer than 12 weeks * Seeking care for low back pain

Exclusion criteria

* Contra indications to physical exercise * Serious spinal pathologies (e.g. tumors, fractures and inflammatory diseases) * Nerve root compromise * Contra indications to the Kinesio Taping (e.g. intolerance to tapes, band aids etc) * Pregnancy * Severe cardiorespiratory conditions

Design outcomes

Primary

MeasureTime frameDescription
Pain IntensityFive weeks after randomizationPain Intensity will be measured by an 11-point (0-10) Numerical Rating Scale (Pain NRS)
DisabilityFive weeks after randomizationDisability associated with low back pain will be measured by the 24-item Roland Morris Disability Questionnaire

Secondary

MeasureTime frameDescription
Pain Intensity3 and 6 months after randomizationPain Intensity will be measured by an 11-point (0-10) Numerical Rating Scale (Pain NRS)
Disability3 and 6 months after randomizationDisability associated with low back pain will be measured by the 24-item Roland Morris Disability Questionnaire
Global impression of recovery5 weeks, 3 and 6 months after randomizationGlobal impression of recovery will be measured by an 11-point (-5 to +5) Global Perceived Effect Scale

Other

MeasureTime frameDescription
Satisfaction with care5 weeks after randomizationSatisfaction with care will be measured by the Medrisk Instrument for Measuring Patient Satisfaction with Physiotherapy Care

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026