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Treatment Program for Chronic Pain

Rehabilitation Program in Individuals with Chronic Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2xx2r2
Enrollment
Unknown
Registered
2019-03-26
Start date
2019-05-01
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

- Group 1 (Motor Control Exercises) - individuals will perform a program of strengthening and stabilization exercises for Core muscles (stabilizers of the lumbar, pelvic and abdominal muscles, and the
n = 200. - Group 2 (Pain Education) - individuals will receive weekly guidance in person and a postural care guide will be provided with information on the importance of staying active and performing
n = 200. - Group 3 (Motor Control Exercises + Pain Education) - individuals will receive intervention through physical exercises and education in pain
n = 200. - Group 4 (Conventional Intervention) - individuals will undergo the usual treatment through resources and application of conventional techniques
n = 200. - Control Group - Individuals who can not participate in any intervention for their own reasons will be monitored for the symptoms and variables studied
n = 100. The interventions will be applied in 16 sessions, twice a week, totaling 8 weeks of treatment, with an average duration of 40 minutes.
Other
E02.760.169.063.500.387
E02.779

Sponsors

Universidade do Estado de Santa Catarina
Lead Sponsor
Prefeitura Municipal de São José
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: History of low back pain in the last six months and pain intensity igual ou maior que 3 (Numeric Pain Rating Scale - NPRS) on movement in at least one direction (flexion, extension or rotation).

Exclusion criteria

Exclusion criteria: Previous history of rheumatic disease, lumbar myelopathy, tumors, central or peripheral neurological disorders; history of major trauma, fracture or surgery in the lumbar region; signs of nerve root compression such as: major muscle weakness affecting the lower limb, decreased or abolished patellar and calcaneal reflexes, and decreased sensitivity in the lower limb dermatomes.

Design outcomes

Primary

MeasureTime frame
To evaluate the subjective intensity of pain through the "Numeric Pain Rating Scale - NPRS" after 8 weeks of treatment. We will see if the numbers will reduce, increase or remain the same comparing moments before and after intervention.

Secondary

MeasureTime frame
To evaluate the threshold of pressure pain through digital algometer, disability, fear and avoidance beliefs, kinesiophobia, quality of life, mood condition, levels of depression and anxiety, quality and behavior of sleep through questionnaires that will be applied by the researchers.

Countries

Brazil

Contacts

Public ContactMaíra Cunha

Universidade do Estado de Santa Catarina

mairajunkes@gmail.com+55-4836648677

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 13, 2026