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Clinical Trials in Brazil / NCT07584564
Starting soon Not applicable

Application of the Concept of Proprioceptive Neuromuscular Facilitation in Trunk Control in Patients Admitted to the ICU.

NCT07584564 · tracked via the Priya Life Science Brazil tracker
Phase
Not applicable
Started
2026-06-01
Last updated
2026-05-22

Condition(s) studied

Intensive Care Unit Acquired Weakness

Investigational drug(s) / intervention(s)

Proprioceptive Neuromuscular Facilitation (PNF)Standard physiotherapy

Proprioceptive Neuromuscular Facilitation (PNF): From its beginnings, PNF has successfully integrated many of the concepts of contemporary neurorehabilitation interventions. The Philosophy and Basic Principles of PNF, together with the specific spiral and diagonal patterns, make up the cornerstone of PNF. PNF also includes motor learning and functional retention of newly learned activities with the repetition of a specific demand; the use of the developmental progression of motor behavior that enables patients to create and re-create strategies of efficient functional movement; and the biomechanical and behavioral analysis of motor control. All activities within PNF intervention are directed towards a functional goal and are relative to the environment in which the goal is to be achieved.

Standard physiotherapy: This group will undergo conventional physiotherapy according to institutional protocol.

Study summary

Muscle weakness acquired in the ICU (FAUTI) is related to the functional decline of patients admitted to an Intensive Care Unit (ICU). For better follow-up, scales such as (Chelsea Critical Care Physical Assessment) CPAx and (Medical Research Council) MRC help to identify early the muscle and functional impairment of these patients. Early mobilization aims to minimize these effects and therefore the search to reach the highest mobility milestone is constant bedside sitting (BSS) is an important milestone in recovery, associated with better functional results when there is good trunk control, as the coordinated activation of muscles in this region is essential for stabilization and reaching higher postures. The physiotherapeutic approach focused on the components of the activities and on the patient's participation is crucial, with the therapeutic option of Proprioceptive Neuromuscular Facilitation (PNF). To evaluate the effect of exercises based on the PNF concept through the Test Control Trunk (TCT) on the trunk balance of patients admitted to the ICU. This is a randomized, crossover clinical trial, carried out at the Pedro Ernesto University Hospital from June 2026 to June 2027. Adults hospitalized for more than 48 hours who meet the inclusion criteria will be screened. and clinical evaluation. The study consists of two blocks of pre- and post-crossover evaluations, conducted by the same blind evaluator. Patients will undergo assessments on the first day of BSS, including assessment of the trunk with TCT and assessment of diaphragm mobility and thickness by ultrasound, before and after intervention (PNF or conventional exercises). Between assessments, there will be a 3-hour rest period.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Over 18 years of age * ICU stay greater than or equal 48 hours; * RASS scale score greater than or equal to -2 and less than or equal to 1; * TCT score less than or equal to 12 points on the "balance in sitting position" score less than or equal to 2 on item 3 "sitting without support". Exclusion Criteria: * Patients in a coma, with spinal cord instability, metastases, and bone lesions; * Neuromuscular or neurological diseases * Discharge from the general ICU before SBL * Proportional care phase 3; * Readmissions to the general ICU;

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Pedro Ernesto University Hospital Rio de Janeiro Rio de Janeiro

More Universidade Federal do Rio de Janeiro trials in Brazil

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07584564 on ClinicalTrials.gov ↗ ← All trials in Brazil