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Effect of respiratory training on quality of life of patients with traumatic spinal cord injury: a randomized controlled trial.

Effect of inspiratory muscular training on quality of life of patients with traumatic spinal cord injury: a randomized clinical trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-54bvbb
Enrollment
Unknown
Registered
2019-06-07
Start date
2018-08-21
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

The intervention will be performed through inspiratory muscle training (IMT) using equipment with adjustable load. For the training group (GTMI), respiratory muscle training will be performed with an
Other
E02.190.525.186

Sponsors

Universidade de Brasília-FCE
Lead Sponsor
Universidade de Brasília-FCE
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: The male and female, with traumatic spinal cord injury, with complete injury (ASIA A or B) between the C4 and T4 levels occurred for at least 6 months.

Exclusion criteria

Exclusion criteria: Patients in programming surgical, portators of cardiopatia or pneumoopatia, sleep with infecciosas agudas or com any descompensation clinical, sleep, patients have apresentable conditions of can impossibility the training muscular inspiratory.

Design outcomes

Primary

MeasureTime frame
Quality of life will be assessed through two questionnaires (Whodas and Whoqol) applied before and after intervention, with variation in the scores of the questionnaire scores. Proposal of data collected 24 hours before and after intervention.;Improvement of respiratory muscle strength assessed by means of manovacuometry, with a variation of at least 5% of maximal inspiratory and expiratory pressures before and after the intervention.Proposal of data collected 24 hours before and after intervention.

Secondary

MeasureTime frame
Improvement of pulmonary capacity assessed by spirometry, with variation of at least 5% forced vital capacities, forced expiratory volume and relationship between both.Proposal of data collected 24 hours before and after intervention.;An improvement in cardiopulmonary capacity will be assessed by means of the exercise test with a variation of at least 5% of maximal VO2. Proposed data collected 24 to 48 hours before and after intervention.

Countries

Brazil

Contacts

Public ContactAlexandra Miranda

Universidade de Brasília-Faculdade de Ceilândia

alexandra.miranda17@hotmail.com+ 55 61 3107-8937

Outcome results

None listed

Source: REBEC (via WHO ICTRP)