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The effect of pulmonary rehabilitation program on self-efficacy and severity of symptoms among patients with chronic obstructive pulmonary disease

The effect of pulmonary rehabilitation program on self-efficacy and severity of symptoms among patients with chronic obstructive pulmonary disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138905064443N2
Enrollment
66
Registered
2011-05-14
Start date
2010-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic Obstructive Pulmonary Disease (COPD). Other chronic obstructive pulmonary disease

Interventions

Intervention 1: Experimental group participate to pulmonary rehabilitation program that design base on Bandura self efficacy theory. Pulmonary rehabilitation program included self care and self manage
Rehabilitation
Treatment - Other
Experimental group participate to pulmonary rehabilitation program that design base on Bandura self efficacy theory. Pulmonary rehabilitation program included self care and self management education,
The control group received only routine visits and telephone follow up weekly.

Sponsors

Tehran University of Medical Sciences, Iran.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age less than 65 years, verification of diagnosis of moderate to severe COPD according to GOLD criteria (2008), absence of formal exercise training or pulmonary rehabilitation for at least one year prior to the study, no active symptomatic diseases (cardiac disease, musculoskeletal disease, mental disease) that would interfere with the exercise, literate and able to speak Persian, possibility of contact by phone/mobile phone Exclusion criteria: recent exacerbation or change of medication, recent mobility limitation that interferes with exercise, not participating in educational sessions, lack of employing nutritional recommendation or exercise respiratory practice for at least a week

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Self efficacy. Timepoint: before and after intervention. Method of measurement: Chronic Obstructive Pulmonary Disease Self Efficacy Scale (CSES).;Severity of dyspnea. Timepoint: before and after intervention. Method of measurement: Dyspnea Severity Scale.;Severity of fatigue. Timepoint: before and after intervention. Method of measurement: Fatigue Severity Scale (FSS).;Severity of cough. Timepoint: before and after intervention. Method of measurement: Cough Severity Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoumeh Zakerimoghadam

Tehran University of Medical Sciences

zakerimo@sina.tums.ac.ir+98 21 6692 7171

Outcome results

None listed

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