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Effects of Continuous Mobility Training in Prolonged Mechanical Ventilation

NCT05688267 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2023-06-22

No results posted yet for this study

Summary

Background: The exercise intervention can help participants with prolonged mechanical ventilation improve ventilator weaning; however, the content of exercise intervention is diverse and inconsistent.

Objective: This study aims to design the continuous mobility training and examine the clinical effects in participants with prolonged mechanical ventilation.

Methods: This prospective, single-center, concealed allocation, evaluator-blind, randomized control study divided participants transferred from the intensive care unit to the respiratory care center into two groups. The control group underwent the routine ventilator weaning plan and hand bicycle training, while the experimental group underwent routine ventilator weaning plan and continuous mobility training plan. The success rate of ventilator weaning, length of mechanical ventilation, length of stay at the respiratory care center, and total length of hospital stay were analyzed.

Conditions

  • Prolonged Mechanical Ventilation

Interventions

OTHER

Continuous Mobility Training

The continuous mobility training adopted 5 grading exercise level, which was evaluated and implemented by physical therapists, and focused on continuous mobility training courses with different levels. At each stage, the participants were instructed to perform spontaneous breathing exercise, which were confirmed by the physical therapists.

OTHER

Usual Care

Participants of control group formed the routine care group, received the routine mechanical ventilation weaning plan and underwent hand bicycle training.

Sponsors & Collaborators

  • Taichung Tzu Chi Hospital

    lead OTHER

Principal Investigators

  • Chi-Wen Lin · Taichung Tzu Chi Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-01
Primary Completion
2023-06-17
Completion
2023-06-20

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05688267 on ClinicalTrials.gov