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Effect of physical conditioning in patients with spinal cord injury to increase physical resistance.

Effectiveness of aerobic physical training applied to patients with spinal cord injury to increase oxygen consumption.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5tmjnd
Enrollment
Unknown
Registered
2012-01-31
Start date
2010-01-10
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

Spinal Cord Injury

Interventions

42 subjects with spinal cord injury between C5 and L2 segments regions were randomized into two groups. In the intervention group, subjects were submitted to a risk evaluation and effort test before
other
E02.779.483.875

Sponsors

Universidade Estadual de Londrina
Lead Sponsor
Universidade Estadual de Londrina
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Individuals with SCI between segments C5 and L2 according to the classification of the American Spinal Injury Association

Exclusion criteria

Exclusion criteria: Individuals who do regular physical activity, community ambulators and individuals who were unable to pedal the cycle ergometer with their arms.

Design outcomes

Primary

MeasureTime frame
Increase oxygen consumption of intervention group comparing before the start of the study and again after 16 weeks. The stress test was used to measure oxygen consumption and was performed with an upper limb ergometer Cybex ®. The ergometry protocol used was of progressive loads with increments of 150 kilogrameters every 3 minutes of cycling followed by 1 minute of rest after each stage. In each rest phase heart rate and blood pressure were measured. For security reasons, it was chosen to work with the heart rate at 85% or 90% of maximum, accompanied by the perceived exertion scale.

Secondary

MeasureTime frame
Maintenance of oxygen consumption in the control group after 16 weeks.

Countries

Brazil

Contacts

Public ContactEdson Lavado

Universidade Estadual de Londrina

lavado@uel.br55 43 33712288

Outcome results

None listed

Source: REBEC (via WHO ICTRP)