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Efficacy Of Inpatient Pulmonary Rehabilitation Program In Elderly Patients With Acute Exacerbation Of COPD

Efficacy Of Inpatient Pulmonary Rehabilitation Program In Elderly Patients With Acute Exacerbation Of COPD

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07020182
Enrollment
60
Registered
2025-06-13
Start date
2025-06-10
Completion date
2025-09-15
Last updated
2025-06-13

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

Conditions

COPD, COPD Acute Exacerbation, COPD Received PR, Elderly (People Aged 65 or More)

Keywords

Elderly patients with acute exacerbation of COPD

Brief summary

The study aimed to identify the effect of early pulmonary rehabilitation in elderly patients with Acute exacerbation (AE) of COPD (AECOPD) in exercise tolerance, dyspnea, sleep quality, fatigue, and time to discharge from hospital.

Detailed description

A prospective supervised RCT (Randomized Controlled Trial) will be done include elderly COPD patients assigned randomly into two groups; Group A performed Physical therapy program, and Group B is control group completed two daily sessions from day 1 of hospital admission till discharge from the hospital .The study duration will be 12 weeks

Interventions

OTHERphysical therapy program

Group A will performed a physical therapy program that completed two daily sessions till discharge from the hospital .Exercise training starts from randomisation until hospital discharge,and administered twice per day, seven times per week. The study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks

Sponsors

Al-Azhar University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

The codes were determined by using serially numbered block size will be kept in sealed and opaque envelopes in a locked office

Intervention model description

A prospective supervised RCT (Randomized Controlled Trial) will be done include elderly COPD patients assigned randomly into two groups; Group A performed physical therapy program, and Group B is control group completed two daily sessions from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks

Eligibility

Sex/Gender
ALL
Age
65 Years to 78 Years
Healthy volunteers
No

Inclusion criteria

* Patients with acute exacerbation of COPD in both gender * Patient older than 65 years * Patient with clear consciousness * Patients had been diagnosed with shortness of breath or dyspnea that was not caused by heart disease, pneumothorax, or pulmonary edema

Exclusion criteria

* Patient with systolic blood pressure lower than 90 mmHg * Patient with an unstable psychological status, hemoptysis, pneumothorax, pulmonary edema

Design outcomes

Primary

MeasureTime frameDescription
Exercise toleranceThe study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeksThe 6 minute walk test(6MWT)in meter to asses exercise tolerance

Secondary

MeasureTime frameDescription
DyspneaThe study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks(The Modified Medical Research Council (mMRC )scale to assess Dyspnea)
Length of hospital stay(LOS)The study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeks(Number of days to assess length of stay in hospital (LOS) from admission to hospital to discharge from hospital)
Fatigue levelThe study will be start from day 1 of hospital admission till discharge from the hospital.The study duration will be 12 weeksFatigue Severity Scale (FSS)to assess fatigue)

Countries

Egypt

Contacts

Primary ContactMarwa Mohammed, Phd -university lecturer
dr.marwamohammed@p.bsu.edu.eg+201000253865
Backup ContactMarwa Mohammed
dr.marwamohammed@p.bsu.edu.eg

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026