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The Effect of Pulmonary Rehabilitation through Patient Education on Clinical and Spirometric Outcomes in COPD Patients

The Effect of Pulmonary Rehabilitation through Patient Education on Clinical and Spirometric Outcomes in COPD Patients Referred to Alavi Hospital Clinic during 2024–2025

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250816066870N1
Enrollment
258
Registered
2025-09-05
Start date
2024-03-20
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention 1: All patients, following a follow-up visit, will undergo a 3-month program of four training techniques—Postural Drainage, Diaphragmatic Breathing, Chest Vibration, and Directed Cough—at

Sponsors

Abadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion CriteriaDiagnosis of COPD according to GOLD (2025) criteria, in stages I, II, or III. Age over 18 years. Stable COPD condition Ability to correctly perform the recommended exercises. Provision of written informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: Inability to correctly perform the recommended exercises. Presence of another pulmonary disease other than COPD. History of congestive heart failure or coronary artery disease.Presence of orthopedic problems (especially in the lumbar region) or musculoskeletal disorders. Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frame
Change in spirometric indices, particularly FEV1 (Forced Expiratory Volume in 1 second), before and after the intervention. Timepoint: At baseline (start of the study)Three months after follow-up without pulmonary rehabilitation trainingThree months after receiving pulmonary rehabilitation training. Method of measurement: Spirometry.

Secondary

MeasureTime frame
FVC (Forced Vital Capacity) and FEV1/FVC ratioNumber of COPD exacerbationsHistory of hospitalization due to COPD exacerbationClinical symptoms (dyspnea, cough, sputum production, etc.). Timepoint: At baseline (start of the study)--Three months after follow-up without pulmonary rehabilitation training--Three months after receiving pulmonary rehabilitation training. Method of measurement: Spirometry --Researcher-made questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Yahyavi Sahzabi

Abadan University of Medical Sciences

rys.1378@gmail.com+98 61 5326 5357

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026