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How Respiratory Muscle Training can improve care in the Intensive Treatment Units of the Unified Health System

Impact of Respiratory Muscle Training in the ICU for strengthening assistance in the Unified Health System

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4rg8b8p
Enrollment
Unknown
Registered
2025-10-28
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Muscle Strength

Interventions

This is a randomized controlled clinical trial, with open-label masking. The experimental group will consist of 40 patients admitted to an intensive care unit (20 tracheostomized and 20 intubated pati
s inclusion in the study. Initially, data will be collected using a specific form, including: demographic information (age, sex, and ethnicity)
clinical history (ICU admission diagnosis, previous comorbidities, smoking and alcohol use history)
prior functional status (Glasgow Coma Scale, Johns Hopkins Mobility Scale)
current clinical data (ICU length of stay, duration of mechanical ventilation until inclusion in the study, use of muscle relaxants, level of consciousness, vital signs such as heart rate, respiratory
relevant laboratory test results (arterial blood gas, serum electrolytes, blood count)
ICU-related complications (presence of ventilator-associated pneumonia, delirium, or multiple organ dysfunction syndrome)
use of medications

Sponsors

Universidade Estadual de Goiás
Lead Sponsor
Centro Estadual de Reabilitação e Readaptação Dr. Henrique Santillo- CRER
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age 18 years or older; both sexes; hemodynamically stable; using an artificial airway device (orotracheal tube or tracheostomy); on mechanical ventilation with ventilatory parameters favorable for the initiation of the weaning process (PSV mode)

Exclusion criteria

Exclusion criteria: Participants with any type of neuromuscular disease; with contraindications to respiratory exercise for respiratory muscle training; dependent on controlled modes of mechanical ventilation; and under deep sedation

Design outcomes

Primary

MeasureTime frame
It is expected that there will be a greater gain in respiratory muscle strength in the experimental group, as verified through manovacuometry after a period of respiratory muscle training

Secondary

MeasureTime frame
It is expected to observe a shorter duration of mechanical ventilation, reduced length of hospital stay, and lower incidence of pulmonary complications.

Countries

Brazil

Contacts

Public ContactDaniella Vento

Universidade Estadual de Goiás- ESEFFEGO

daniella.vento@ueg.br+5562982439115

Outcome results

None listed

Source: REBEC (via WHO ICTRP)