Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07189260

Pre- and Postoperative Chest Therapy With Positive Expiratory Pressure (PEP) to Prevent Hospital-acquired Pneumonia

Led by University Hospital Bispebjerg and Frederiksberg · Updated on 2025-09-23

566

Participants Needed

2

Research Sites

358 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to investigate whether pre- and postoperative treatment with systematic PEP therapy can prevent hospital-acquired pneumonia in patients with hip frac-ture. It will also learn about the barriers regarding PEP therapy in this group of patients. * Does pre- and postoperative treatment with systematic PEP therapy prevent hospital-acquired pneumonia in patients with hip fracture? * Which barriers do participants have regarding PEP therapy in this group of patients? Researchers will compare systematic PEP therapy to no intervention besides standard treat-ment to see if systematic therapy with PEP can prevent hospital-acquired pneumonia. Participants will: * Receive systematic PEP therapy during hospitalization or no intervention besides standard treatment * Register the PEP therapy four times daily on a paper checklist. Failure to perform the treatment and the reason must also be documented on the checklist.

CONDITIONS

Official Title

Pre- and Postoperative Chest Therapy With Positive Expiratory Pressure (PEP) to Prevent Hospital-acquired Pneumonia

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Hip fracture regardless of age
  • Cognitively well-functioning
  • Able to understand the study and give informed consent
  • Able to speak and understand Danish
  • Resident of Region Hovedstaden or Region Sjælland
Not Eligible

You will not qualify if you...

  • Cognitively impaired
  • Unable to understand the study and give informed consent
  • Pneumonia upon admission
  • Delirium upon admission
  • Pneumothorax
  • For patients with dementia or brain injury, ability to give informed consent will be assessed individually

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Bispebjerg & Frederiksberg Hospital

Copenhagen, Denmark, 2400

Actively Recruiting

2

Herlev & Gentofte Hospital

Herlev, Denmark, 2730

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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