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Immediate effects of Spinal Manipulation on pain and balance in individuals with Chronic Low Back Pain

Immediate effects of Vertebral Manipulation on painful sensitivity and postural stability of individuals with Chronic Low Back Pain - randomized controlled clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3ksq2c
Enrollment
Unknown
Registered
2020-07-13
Start date
2020-09-01
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

Low back pain

Interventions

A total of 80 individuals participated in the research. Participants will be randomly allocated to two groups of 40 members: group 1 (will receive a lumbar spinal manipulation technique in a hypo mobi
Other
E02.190.599

Sponsors

Centro Universitário Augusto Motta
Lead Sponsor
UniGuairacá Centro Universitário
Collaborator

Eligibility

Age
18 Years to 59 Years

Inclusion criteria

Inclusion criteria: Low back pain lasting at least three months; score on the numerical pain scale of at least 3 points at the time of assessment; age between 18 and 59 years; hypomobility in at least one lumbar vertebral segment verified during the physiotherapeutic evaluation through the posteroanterior pressure test in the prone position (Spring Test); symptoms that do not extend beyond the knee; absence of neuropathic pain components assessed using the painDETECT questionnaire.

Exclusion criteria

Exclusion criteria: Chronic widespread pain; ligament laxity or hyper flexibility; pregnancy; conditions that contraindicate the use of vertebral manipulation techniques at high speed and low amplitude (red flags) such as vertebral fractures, cauda equina syndrome, cancer, inflammatory rheumatic diseases, vertebral infections, bone tuberculosis; any condition that may interfere with pain sensitivity measures, for example, changes in skin sensitivity, neurological diseases, psychiatric diseases or fibromyalgia; any condition that interferes with body balance, for example, neurological diseases or vestibulopathy.

Design outcomes

Primary

MeasureTime frame
Increase in the pressure pain limit controlled with a pressure algometer from the observation of a variation of at least 15% in the pressure pain limit in the pre and post-intervention measurements. They will be evaluated bilaterally as following regions: middle part of the medial gastrocnemius muscle, anterior tibial muscle laterally at the level of the anterior tibial tuberosity, two sides laterally to the L5 spine process, two sides laterally to the L1 spine process, medium deltoid pattern, two pieces distal to the lateral epicondyle.;Improved postural stability, assessed by decreasing the oscillation of the body's pressure center (CoP) through baropodometry from the observation of a variation of at least 15% in the pre and post-intervention measurements. The stability variables investigated by means will be the CoP ellipse area (mm2), the standard deviation of the amplitude (mm) of the displacement of the CoP Antero/Posterior, and Medio/Lateral.

Secondary

MeasureTime frame
A decrease in pain intensity assessed by the visual analog pain scale from the observation of a variation of at least 2 points in the pre and post-intervention assessment.

Countries

Brazil

Contacts

Public ContactJOAO FREITAS

UniGuairacá Centro Universitário

jpfreitas06@gmail.com+55-042-99194653

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 12, 2026