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Responsiveness of clinical outcomes and Functional Tests in older people with Chronic Low Back Pain

Investigating Central Sensitization mechanisms in elderly with Chronic Low Back Pain after an Active Exercise Program

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9prhzng
Enrollment
Unknown
Registered
2021-07-05
Start date
2021-07-07
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

Back pain

Interventions

Sponsors

Universidade Federal de Minas Gerais
Lead Sponsor
Universidade Federal de Minas Gerais
Collaborator

Eligibility

Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with low back pain seeking care in health services in Belo Horizonte Minas Gerais; Pain or discomfort located between the last rib and above the lower gluteal fold with or without pain in lower limbs; Pain or discomfort for at least three months; Patients with common imaging findings, such as osteoarthritis, grade I spondylolysis and spondylolisthesis or protrusion / hernia / prolapse disc, but with clinical symptoms that meet the inclusion

Exclusion criteria

Exclusion criteria: Patients who have had recent spine surgery or knowledge or suspicion of severe spinal pathology, such as fracture, metastasis, inflammatory or infectious diseases of the spine, cauda equina syndrome, radiculopathy (at least two of the following signs: weakness, reflex change or loss of sensation associated with the same spinal nerve); Patients with any contraindications to exercise in accordance with American College of Sports Medicine guidelines

Design outcomes

Primary

MeasureTime frame
Mobility will be measured with the Timed ‘’Up and Go’’ test. The patient starts in a seated position. Then, the patient stands up upon therapist’s command: walks 3 meters, turns around, walks back to the chair and sits down. The time stops when the patient is seated.;Mobility will be measured with the Timed usual walking speed on a 4-meter course. The participant will be instructed to walk, at their usual speed, for a distance of 4 meters. The time to complete the task is recorded by the assessor.;Mobility will be measured with the five Times Sit to Stand Test. The participant is instructed to do sit-to-stand five times. The time to complete the task is recorded by the assessor.;Disability will be measured using The Roland Morris Disability Questionnaire. This questionnaire consists of 24 yes/no items with a total score ranging from 0 (no disability) to 24 (maximal disability).;The global perceived effect scale (GPES) will be collected after treatment to assess each participant’s perception of recovery. Participants will be asked, “Compared to your symptoms at the baseline assessment, how would you describe your back these days?” The GPES varied from –5 (vastly worse) through 0 (no change) to 5 (completely recovered).

Secondary

MeasureTime frame
Secondary outcomes are not expected.

Countries

Brazil

Contacts

Public ContactRafael Pinto

Universidade Federal de Minas Gerais

rafaelzp@ufmg.br+55 31 3409 7405

Outcome results

None listed

Source: REBEC (via WHO ICTRP)