Skip to content

Effectiveness of Electrical Stimulation or Kinesio Taping on Recovery Disability in Low Back Pain

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02812459
Acronym
ELECBACK
Enrollment
62
Registered
2016-06-24
Start date
2016-06-30
Completion date
2018-04-30
Last updated
2018-10-09

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

Conditions

Chronic Low Back Pain

Keywords

Electrical Stimulation Therapy, Kinesio taping, Exercise

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

Interventions

OTHERKinesio taping

Kinesio taping is a new taping modality which act diminishing pain.

OTHERElectrical Stimulation

Electrical stimulation therapy is a electrical current that allow patients diminish pain.

Sponsors

Universidad de Granada
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. LBP for three months or more; 2. age between 25 and 65 years; 3. a score of four points or more on the Roland Morris Disability Questionnaire; 4. not currently receiving physical therapy.

Exclusion criteria

1. the presence of lumbar stenosis; 2. any clinical signs of radiculopathy; 3. a diagnosis of spondylolisthesis; 4. a diagnosis of fibromyalgia; 5. treatment with corticosteroid or oral medication within the past two weeks; 6. a history of spinal surgery; 7. disease of the central or peripheral nervous system.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Roland Morris Disability Questionnaire (RMDQ) at one month.4 weeksThe 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

MeasureTime frameDescription
Change from baseline Visual Analogue Scale (VAS) at one month4 weeksThe visual analogue scale for pain intensity ranged from 0 = no pain to 10 = worst imaginable pain
Change from baseline Tampa Scale for Kinesiophobia (TSK) at one month4 weeksThe Tampa Scale for Kinesiophobia comprises 17 items on the fear of movement or recurrent lesion, each scored on a 4-point Likert scale from completely disagree to completely agree.
Change from baseline Pressure pain thresholds (PPT) at one month4 weeksExamination of PPT will be performed with the use of an Algometer. According to International Association for the Study of Pain, PPT is the smallest stimulus causing the feeling of pain (International Association for the Study of Pain, Subcommittee on Taxonomy, 1986). The examination will carried out twice in the same places, on the left and right sides following the protocol described by Sipko et al.2013: musculus erector spinae - at the level of L2, 3 cm away from the interspinous line; musculus gluteus medius - between the greater trochanter and iliac crest sideways; musculus triceps surae - the transition of the belly of the muscle into the tendon; and musculus tibialis anterior - one-third of the upper shank, at the front.
Change from baseline Oswestry Disability Index (ODI) at one month.4 weeksThe Oswestry disability index evaluates daily life activity limitations in 10 dimensions, each scored on a 6-point scale (0-5 points); the total points scored are expressed as a percentage, used to classify individuals as minimally disabled (0-10%), moderately disabled (20-40%), severely disabled (40-60%), crippled (60-80%), or bedbound (80-100%).
Change from baseline Mechanosensitive/straight-leg raise neurodynamic testing at one month4 weeksThe subject will be positioned in supine with standardized head support. After the test will be performed with the ankle in neutral position and with 30º of ankle flexion. The hip will be flexed with the knee extended until the subject reports onset of neural-mediated symptoms. The degree of hip flexion will be measured with a large universal goniometer.
Change from baseline Anxiety and depression measures at one month4 weeksBeck questionnaire
Change from baseline Quality of Sleep at one month4 weeksPittsburgh questionnaire
Change from baseline Mechanosensitive/the Seated Slump Test neurodynamic testing at one month4 weeksThe subject will be positioned in an erect sitting position on an examination plinth with the popliteal creases just off the edge of the plinth. The subject will be asked to sit in a slouched position. After, the subject will be asked to actively flex the cervical spine as far as comfortably possible. After, the subject's ankle will be then passively dorsiflexed to slight resistance, while the knee is slowly passively extended.The knee will be extended until the subject reports onset of neural-mediated symptoms.The degree of knee extension will be measured with a large universal goniometer.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026