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Effect of Pulmonary Rehabilitation in Females With Acute Exacerbation of COPD Induced by Biomass Fuel Smoke

Effect of Pulmonary Rehabilitation in Females With Acute Exacerbation of COPD Induced by Biomass Fuel Smoke Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07509736
Acronym
AECOPD BIOMASS
Enrollment
60
Registered
2026-04-03
Start date
2026-03-20
Completion date
2026-06-20
Last updated
2026-04-03

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

Conditions

AECOPD, BIOMASS FUEL, Pulmonary Rehabilitation

Keywords

AECOPD-Anexity-depression-Biomass fuel

Brief summary

COPD represents an important public health challenge that is both preventable and treatable. GOLD is committed to improving the health of people at risk of and with COPD, wherever they happen to have been born, and wishes to do its bit to help achieve the United Nations Sustainable Development Goal to reduce premature mortality from non-communicable diseases - including COPD - by one third by 2030. GOLD aims in stable COPD to relieve symptoms, improve exercise tolerance and improve health status. Non-pharmacological interventions for those high-risk groups of patients, studies of intervention strategies both during inpatient stay and shortly after discharge have been undertaken, to decrease readmission rates and improve QOL, including disease-specific self-management, pulmonary rehabilitation, and early medical follow-up.Seeking for allow cost way to alleviate patients' symptoms in order to increase independence and QOL.

Detailed description

The study aimed to identify the effect of pulmonary rehabilitation on exercise tolerance, anxiety, depression, dyspnea and time to discharge from hospital in a group of COPD females admitted to inpatient wards till discharge from hospital.

Interventions

OTHERIntervention 1 → Arm 1 (pulmonary rehabilitation group).

Arm1: pulmonary rehabilitation group participants will perform physical therapy program and receive standardized pulmonary rehabilitation. Intervention(s): pulmonary rehabiliation program

Sponsors

Beni-Suef University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Intervention model description

Females in group A will receive In-patient interdisciplinary standardized pulmonary rehabilitation program included breathing exercises, bronchial hygiene, health education, low-load resistance exercise (15%-30% of 1 repetition maximum (1-RM) as tolerated), aerobic training in the form of walking exercise under supervision of physiotherapist with intensity of rate of perceived dyspnea (RPD) of 4-6 (10 points scale), duration of 20 minutes or as tolerated \[30\].While group B will b control group only receive medical treatment

Eligibility

Sex/Gender
FEMALE
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Only females diagnosed with a history of using biomass fuel for cooking and heating during their lifetime with no history of smoking or being Ex smoker nor a non-smoker. * Participants in clear consciousness. * participants diagnosed with shortness of breath or dyspnea that was not caused by heart disease, pneumothorax, or pulmonary oedema

Exclusion criteria

* Systolic blood pressure lower than 90 mmHg. * Participants with unstable psychological status, hemoptysis, pneumothorax, pulmonary edema.

Design outcomes

Primary

MeasureTime frameDescription
Exercise tolerance2 months (8 weeks)It measures functional capacity and exercise tolerance and it measured by 6 minutes walk test usually participants walk in 30 meters distance in the usual waling pace

Contacts

CONTACTMarwa Mohammed Mohammed Eleawa, Assistant professor
dr.marwamohammed@pt.bsu.edu.eg01000253865

Outcome results

None listed

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