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Application of exercises after cardiovascular surgery

Application of a mobilization protocol, based on the functional level, after cardiovascular surgery: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-29495g
Enrollment
Unknown
Registered
2020-02-27
Start date
2020-01-27
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

cardiac and vascular surgeries

Interventions

All of 60 participants will be followed from admission to discharge, using a control form. Participants will be assessed in 5 moments: preoperative (T1), during SICU stay (T2), at SICU discharge (T3),
quality of life, through the Short Form 36
and level of physical activity, through the Baecke questionnaire. At T2, randomization into two groups, control or intervention, will be done. Also will be recorded the severity status using APACHE II
Other
A07.015.461.165

Sponsors

Hospital Universitário da Universidade Federal do Maranhão
Lead Sponsor
Hospital Universitário da Universidade Federal do Maranhão
Collaborator

Eligibility

Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Adults patients admitted to the ICU after cardiac surgery (myocardial revascularization, valve replacement / repair, correction of thoracic aortic diseases and combined procedures) or vascular surgery (revascularization of upper / lower limbs and correction of abdominal aortic diseases), from January 2020 to June 2021, with modified Barthel index for walking ? 4 will be included

Exclusion criteria

Exclusion criteria: Cardiorespiratory arrest Brain injury, with motor response <5 (Glasgow coma scale) Recent acute myocardial infarction Unstable fractures Pregnancy Medical guidelines for maintaining absolute rest due to patient severity Unable to understand verbal commands Mechanical ventilation time for more than 24 hours Enrollment in another clinical study

Design outcomes

Primary

MeasureTime frame
Decrease at least 20% of the time elapsed, measured in hours, to achieve the following mobilization milestones: edge of bed sitting, bedside sitting, orthostatism and walking.

Secondary

MeasureTime frame
Maintaining of peripheral muscle strength, assessed by handgrip dynamometry, comparing to preoperative period ;Lower frequency o ICU acquired weakness, using as criteria values under 11kgF, in men, and 7 kgF in women, during evaluation by handgrip dynamometry. ;Highest ICU Mobility Scale score at ICU discharge of at least 1,4 points ;Decrease in 1-2 days of ICU and hospital lenght of stay ;Better quality of life in 20% after 3 months of hospital discharge measured by SF-36 questionnaire

Countries

Brazil

Contacts

Public ContactMayara Gabrielle Borges

Hospital Universitário da Universidade Federal do Maranhão

mayaragabriellebs4@gmail.com+559821091098

Outcome results

None listed

Source: REBEC (via WHO ICTRP)