Skip to content

Assessment of the effects of TENS in patients with low back pain treated with acupuncture.

The assessment of the effects of analgesia in transcutaneous electrical stimulation associated with acupuncture in patients with chronic low back pain.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-84jx98
Enrollment
Unknown
Registered
2016-09-12
Start date
2016-09-10
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

The study is conducted in humans diagnosed with low back pain, belonging to the target population of adults

Interventions

Three groups of patients, each consisting of 15 patients will undergo acupuncture sessions - totaled 10 for each patient in each group - will be carried out by the researcher, and used a total of 6 do
also used bilaterally. Will be evaluated during each session, possible adverse events associated with acupuncture, including: pain, dizziness, nausea, sweating, among others. The groups of patients ev
the G.2: receive acupuncture treatment associated with TENS and G.3: you receive TENS treatment only. All sessions in all groups will last 20 minutes. Treatment with transcutaneous electrical stimulat
Other

Sponsors

Universidade Federal de Pernambuca - UFPE/ Brasil
Lead Sponsor
Universidade Federal de Pernambuca - UFPE/ Brasil
Collaborator

Eligibility

Age
40 Days to 64 Months

Inclusion criteria

Inclusion criteria: Patients aged from 40 years; both sexes; with a history of low back pain for more than three months.

Exclusion criteria

Exclusion criteria: In addition to not meet the inclusion, they will also be considered affected or carriers of any concomitant arthropathy; those who are undergoing cancer treatment; which have chronic diseases or changes in neurological examination as Parkinson's disease, Alzheimer's and Stroke rehabilitation. Also excluded are patients who do not accept (or their relatives) sign the consent form.

Design outcomes

Primary

MeasureTime frame
Identify the most used technique provides time without pain to the patient. Waiting as final outcome the reduction of pain in these patients.

Secondary

MeasureTime frame
The pain reduction of patients and the improvement in quality of life thereof, determined by the SF-12 quality of life questionnaire at baseline and end of study.;Through analog pain scale (EVA), inform the visual and personal aspect of pain that each patient has

Countries

Brazil

Contacts

Public Contactwecsley guilherme da mota

Universidade Federal de Pernambuco

wguilhermem@hotmail.com+55(81)95903464

Outcome results

None listed

Source: REBEC (via WHO ICTRP)