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Cryotherapy and TENS on Low Back Pain

Immediate Effects of Conventional TENS and Burst TENS Combined With Cryotherapy in the Non-specific Low Back Pain

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03248505
Acronym
CTLBP
Enrollment
120
Registered
2017-08-14
Start date
2017-05-29
Completion date
2018-02-28
Last updated
2017-08-14

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

Conditions

Low Back Pain, Mechanical

Brief summary

This study aim analyze the immediate effects of conventional transcutaneous electrical nerve stimulation (TENS) and Burst TENS combined or not with cryotherapy in patients with non-specific low back pain. All subjects will be submitted to an evaluation of the painful sensation, through the numerical rating scale, and pain threshold, through algometry, before, immediately after the intervention and 25 minutes after.

Interventions

Transcutaneous Electrical Nerve Stimulation (frequency of 100 Hz, pulse duration of 100 micro-seconds and sensory-level amplitude) with two electrodes in each side of the lumbar spinal.

DEVICEBurst TENS

Burst-modulated TENS with carrier frequency of 100 Hz, burst-modulated at 4Hz, pulse duration of 200 micro-seconds and motor-level amplitude.

OTHERCryotherapy

1,5 Kg of crushed ice pack on lumbar spine.

DEVICEBurst TENS + Cryotherapy

Burst-modulated TENS with carrier frequency of 100 Hz, burst-modulated at 4Hz, pulse duration of 200 micro-seconds and motor-level amplitude plus 1,5 Kg of crushed ice pack on lumbar spine.

DEVICEConventional TENS + Cryotherapy

Transcutaneous Electrical Nerve Stimulation (frequency of 100 Hz, pulse duration of 100 micro-seconds and sensory-level amplitude) plus s 1,5 Kg of crushed ice pack on lumbar spine.

TENS device turned on, but with zero amplitude.

Sponsors

Universidade Federal do Rio Grande do Norte
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

3x6

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Aged between 18 and 50 years; * Have chronic non-specific low back pain.

Exclusion criteria

* Serious spinal pathologies (fractures, tumors, and inflammatory pathologies such as ankylosing spondylitis); * Nerve root compromise (disc herniation and spondylolisthesis with neurological compromise, spinal stenosis, and others); * Fibromyalgia * Corticosteroid treatment in the previous two weeks; * Antiinflammatory treatment in the previous 24 hours; * Contraindications to the use of Kinesio Taping (allergy or intolerance); * Score of three or less on Visual Analogue Scale of the first day; * Pregnancy; * Ice allergy.

Design outcomes

Primary

MeasureTime frameDescription
Painful sensationEvaluation of pain sensation 25 minutes after the application of the intervention.Pain sensation measured by pain numerical rating scale

Countries

Brazil

Contacts

Primary ContactJamilson S Brasileiro, PhD
brasileiro@ufrnet.br+55 84 3342-2015

Outcome results

None listed

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