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Clinical Trials/NCT06412081
NCT06412081
Recruiting
Not Applicable

The Value of Point-of-care Lung Ultrasound for Physiotherapy in Hospitalized Patients With Acute Respiratory Symptoms

Cliniques universitaires Saint-Luc- Université Catholique de Louvain2 sites in 1 country30 target enrollmentMay 10, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Complication
Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Enrollment
30
Locations
2
Primary Endpoint
Percentage of change of treatment plan
Status
Recruiting
Last Updated
5 days ago

Overview

Brief Summary

This study aims to evaluate the relevance of using point-of-care lung ultrasound (LUS) in modifying the physiotherapist's treatment plan for patients hospitalized in a general ward.

Detailed Description

Hospitalized patients often confront respiratory issues stemming from diverse causes, such as pneumonia. Physiotherapists rely on a range of clinical and imaging data to inform their treatment decisions. Yet, they face challenges due to the absence of readily accessible, sensitive, specific, and reliable measurements to tailor the most effective physical therapeutic interventions based on individual clinical scenarios. Point-of-care Lung Ultrasound (LUS) holds promise in addressing these existing gaps. This study aims to evaluate the impact of integrating LUS into clinical practice by comparing physiotherapists' initial clinical assessments and treatment plans with those made after incorporating LUS findings in patients admitted to a general ward.

Registry
clinicaltrials.gov
Start Date
May 10, 2024
End Date
December 30, 2026
Last Updated
5 days ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Responsible Party
Principal Investigator
Principal Investigator

William Poncin, PT, PhD

PhD

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Eligibility Criteria

Inclusion Criteria

  • Hospitalization in a general ward
  • Acute respiratory symptoms (\< 48h)
  • Chest X-ray available within 24h before or after the use of LUS

Exclusion Criteria

  • Any conditions precluding the use of LUS (thoracic skin lesions, thoracic bandage, subcutaneous emphysema)
  • Inability to understand instructions due to cognitive impairment or due to language barrier

Outcomes

Primary Outcomes

Percentage of change of treatment plan

Time Frame: Before and Immediately after the use of LUS (10-min interval)

Relative change of treatment plan after the results of LUS in relation to the total number of events

Secondary Outcomes

  • Agreement between the events observed on LUS and the events observed on Chest X-Ray(At baseline)

Study Sites (2)

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