Ireland
--:--IST
Latest
Clinical Trials in Brazil / NCT05459376
Starting soon Not applicable

Effect of Dry Cupping Therapy Associated With the McKenzie Method in Patients With Chronic Low Back Pain

NCT05459376 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2026-01-01
Last updated
2025-04-02

Condition(s) studied

Low Back Pain

Investigational drug(s) / intervention(s)

Exercises and dry cupping

Exercises and dry cupping: Participants in the intervention group will receive an assessment, classification as to MDT syndrome and indication of the preferred direction of movement, whether flexion, extension or lateral displacement of the spine

Study summary

Introduction: Currently, clinical practice guidelines recommend exercise as a first-line approach to the treatment of chronic low back pain (LBP). On the other hand, passive techniques such as cupping therapy have gained space in the management of this population, however, important gaps regarding the combination of cupping therapy with active exercises in individuals with nonspecific chronic low back pain are still present in the literature. In this context, this protocol describes a sham-controlled, randomized and blinded study that aims to evaluate the additional effects of cupping therapy in association with McKenzie method exercises on pain and functional outcomes of individuals with nonspecific chronic low back pain. Methods: 108 individuals with nonspecific and localized chronic low back pain in the age group of 18 to 59 years will be recruited and evaluated, regarding the inclusion and exclusion criteria. Subsequently, they will be randomized to one of 2 groups: intervention group, in which they will be submitted to the McKenzie method intervention and later the addition of the dry suction cup; and sham group, in which, after the intervention of the McKenzie method, the application of the sham cup will be added.

Eligibility

Sex
ALL
Min age
18 Years
Max age
59 Years
Healthy volunteers
No
Inclusion Criteria: * Individuals, male and female, 18 to 59 years, non-obese, with non-specific localized LBP for more than 3 months; * Report pain intensity between 3 and 8 according to the numerical pain scale; Exclusion Criteria: * Have previously performed cupping therapy in some body segment; * Present neurological, vestibular, visual or auditory deficits that make assessments impossible; * Being in the gestational period; * Having severe spinal disease (including fractures, tumour, inflammatory diseases, or tumours); * Have undergone previous spinal surgery; * Present with radiating or sacroiliac back pain; another rheumatic disease such as fibromyalgia,or ankylosing spondylitis.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Marcelo Cardoso de Souza Natal Rio Grande do Norte

More Universidade Federal do Rio Grande do Norte trials in Brazil

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05459376 on ClinicalTrials.gov ↗ ← All trials in Brazil