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Effect of Pursed-Lip Breathing on Physiological Parameters and Discharge Readiness in Children With Pneumonia

Study acronym: PLB-PEDPNEU
StatusCompleted
PhaseNot applicable
Started
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Record History

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  1. Completed without a posted recruiting period Show 7 more changesShow less
    • Final enrollment: 82 participants (planned 66)
    • Primary completion date changed from estimate of Feb 1, 2026 to Mar 30, 2026
    • Study completion date changed from estimate of May 1, 2026 to Jun 30, 2026
    • Start date changed from estimate of Nov 1, 2025 to Jul 1, 2025
    • Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 1 of 1 entry
    • Site details revised
  2. Lead sponsor: Türkan Kadiroğlu to Ataturk Universityv2 Show 4 more changesShow less
    • Start date: Sep 15, 2025 to Nov 1, 2025
    • Primary completion date: Jan 15, 2026 to Feb 1, 2026
    • Study completion date: Jun 15, 2026 to May 1, 2026
    • Site details revised
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study aims to evaluate the effects of Pursed-Lip Breathing (PLB) exercises on physiological parameters (such as respiratory rate, heart rate, and oxygen saturation) and discharge readiness in children diagnosed with pneumonia. The study is designed as a randomized controlled trial involving pediatric patients between the ages of 3 and 4. The intervention includes guided PLB exercises performed twice daily for three consecutive days. Data will be collected before and after each session to assess changes in physiological measures and readiness for hospital discharge.
Trial Details
NCT Number NCT07106203
Lead Sponsor Ataturk University
Conditions
(from sponsor)		 Pneumonia
Related terms Pneumonia, Respiratory Aspiration
Enrollment 82 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov