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NCT07484178Not yet recruiting

Effectiveness of Nurse-Led Interventions on Respiratory Outcomes in Hospitalized Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Effectiveness of Nurse-Led Interventions on Respiratory Outcomes in Hospitalized Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Randomized Control Trial

Source: ClinicalTrials.gov · Last updated 15 Apr 2026

Brief summary (registry, in English)

The goal of this clinical trial is to evaluate whether respiratory nursing interventions can improve respiratory outcomes in patients hospitalized with acute exacerbation of Chronic Obstructive Pulmonary Disease (COPD). The main questions it aims to answer are: Do respiratory nursing interventions improve dyspnea levels measured by the Modified Medical Research Council (mMRC) Dyspnea Scale? Do these interventions improve oxygen saturation and pulmonary function (FVC, FEV1, and FEV1/FVC ratio)? Researchers will compare patients receiving respiratory nursing interventions plus routine hospital care with patients receiving routine hospital care alone to determine whether the interventions improve respiratory outcomes. Participants will: Undergo baseline assessment using the mMRC Dyspnea Scale, pulse oximetry, and pulmonary function tests. Receive either respiratory nursing interventions (deep breathing exercises, chest percussion, postural drainage, and lukewarm water intake) along with routine care or routine hospital care alone. Be reassessed after the intervention period using the same respiratory outcome measures.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
68 (estimated)
First submitted
16 Mar 2026
Start date
2 May 2026
Primary completion date
15 Aug 2026
Lead sponsor
University of Health Sciences Lahore
Diseases
COPD
NCT number
NCT07484178

What you commit to

  • Study type: Interventional
  • Planned participants: 68
  • From 2 May 2026 to the primary completion date, 15 Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Dyspnea due to cardio-pulmonary disease or other co-morbidities.
  • Patients with mental disorders.

Other

  • Patients on mechanical ventilation and ICU admission.
  • Patients with upper airway obstruction.

Who the study is looking for

  • Diagnosed cases of COPD admitted for acute exacerbation according to Global Initiative for Chronic Obstructive Lung Disease.
  • Adults aged \> 40 years (WHO, 2023; GOLD, 2024).
  • Both genders (male \& female).
  • Hemodynamically stable at the time of enrollment in terms of vital signs (e.g., blood pressure \> 90/60 mmHg, heart rate between 60-100 bpm) to safely undergo nursing interventions without acute risk (Jarhyan et al., 2021).
  • Dyspnea Grade ≥ 2 on the mMRC Scale (Mahler and Wells, 1988).
  • Blood Oxygen Saturation (SpO₂) ≥ 88% on Room Air or Oxygen Therapy (O'Driscoll, 2017).

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UHS
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.