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Comparative effects of stretching respiratory accessory muscles and ribs mobilization to improve chest expansion in COPD patients.

Comparative effects of stretching respiratory accessory muscles and ribs mobilization to improve chest expansion in COPD patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220514054851N1
Enrollment
50
Registered
2022-05-27
Start date
2022-06-13
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Chest expansion in COPD.

Interventions

Intervention 1: Intervention group 1 will receive stretching of respiratory accessory muscles. There will be two sets, ten repetitions for each muscle with a one-min interval between them. The sessio

Sponsors

The university of faisalabad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 55 Years

Inclusion criteria

Inclusion criteria: Patients within age group of 30-55 years Patients who are diagnosed with chronic obstructive pulmonary disease according to global initiative for chronic obstructive pulmonary disease Patients with acute and moderate history of chronic obstructive pulmonary disease Both males and females Haemodynamically stable patients who will be willing participate in the study

Exclusion criteria

Exclusion criteria: Patients having lung carcinoma and acute inflammatory condition Patients having cardiac or neuromuscular disease Patients having recent surgery history and recent chest injury Patients having severe or very severe history of chronic obstructive pulmonary disease Corona virus disease of 2019 patients Patients with broken ribs, bruised ribs, fractured ribs Patients having Fibromyalgia Patients with costochondritis Patients having pleurisy

Design outcomes

Primary

MeasureTime frame
Chest expansion. Timepoint: Total 4 weeks of interventional period in which every week 3 sessions and assessment of chest expansion at baseline then after 2 weeks and again after 2 weeks. Method of measurement: Measuring tape.

Secondary

MeasureTime frame
Vital capacity. Timepoint: Total 4 weeks of interventional period in which every week 3 sessions and assessment of chest expansion at baseline then after 2 weeks and again after 2 weeks. Method of measurement: Spirometry.;Dyspnea. Timepoint: Total 4 weeks of interventional period in which every week 3 sessions and assessment of chest expansion at baseline then after 2 weeks and again after 2 weeks. Method of measurement: Modified borg dyspnea scale.

Countries

Pakistan

Contacts

Public ContactDr Sidra Majeed

The university of faisalabad

rabiaanwar853@gmail.com+92 300 8431018

Outcome results

None listed

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