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Clinical Trials/NCT02812459
NCT02812459CompletedNot Applicable

Short-term Effectiveness of Additional Electrical Stimulation to Exercise Versus Kinesio Taping in Patients With Chronic Low Back Pain: A Randomized Controlled Trial

Universidad de Granada1 site in 1 country62 target enrollmentStarted: June 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
62
Locations
1
Primary Endpoint
Change from baseline in Roland Morris Disability Questionnaire (RMDQ) at one month.

Study Overview

Brief Summary

The purpose of this study is to analyze the effectiveness of electrical stimulation and kinesio taping in combination with exercise in People with Chronic Low Back Pain

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
25 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • LBP for three months or more;
  • age between 25 and 65 years;
  • a score of four points or more on the Roland Morris Disability Questionnaire;
  • not currently receiving physical therapy.

Exclusion Criteria

  • the presence of lumbar stenosis;
  • any clinical signs of radiculopathy;
  • a diagnosis of spondylolisthesis;
  • a diagnosis of fibromyalgia;
  • treatment with corticosteroid or oral medication within the past two weeks;
  • a history of spinal surgery;
  • disease of the central or peripheral nervous system.

Arms & Interventions

Kinesio taping plus exercise

Experimental

Kinesio taping application for low back plus back exercises.This protocol will be administered three a week for 4 weeks.

Intervention: Kinesio taping (Other)

Electrical stimulation plus exercise

Active Comparator

Electrical stimulation for control pain applied in low back plus exercises.This protocol will be administered three a week for 4 weeks.

Intervention: Electrical Stimulation (Other)

Outcomes

Primary Outcomes

Change from baseline in Roland Morris Disability Questionnaire (RMDQ) at one month.

Time Frame: 4 weeks

The Roland Morris disability questionnaire is a self-administered disability measurement scored on a 24-point scale from 0 = no disability to 24 = severe disability

Secondary Outcomes

  • Change from baseline Anxiety and depression measures at one month(4 weeks)
  • Change from baseline Visual Analogue Scale (VAS) at one month(4 weeks)
  • Change from baseline Pressure pain thresholds (PPT) at one month(4 weeks)
  • Change from baseline Tampa Scale for Kinesiophobia (TSK) at one month(4 weeks)
  • Change from baseline Oswestry Disability Index (ODI) at one month.(4 weeks)
  • Change from baseline Quality of Sleep at one month(4 weeks)
  • Change from baseline Mechanosensitive/the Seated Slump Test neurodynamic testing at one month(4 weeks)
  • Change from baseline Mechanosensitive/straight-leg raise neurodynamic testing at one month(4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Encarnación Aguilar Ferrandiz

Lecturer

Universidad de Granada

Study Sites (1)

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