The effect of self management program on indicators of clinical status in patients with chronic obstructive pulmonary disease

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013061713694N1

Enrollment

Registered

2013-08-11

Start date

2012-11-21

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. chronic obstructive pulmonary disease, unspecified

Interventions

Intervention 1: Intervention Group: Providing an educational pamphlet plus receive of self management program based on 5A model in the term of 12 weeks, in 5 stage: Assess, Advise, Agree, Assist, Arra

Behavior

Intervention Group: Providing an educational pamphlet plus receive of self management program based on 5A model in the term of 12 weeks, in 5 stage: Assess, Advise, Agree, Assist, Arrange.

Control Group: providing an educational pamphlet

Eligibility

Sex/Gender

All

Age

45 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: COPD confirmed by physician; age between 45-70 years; having a BMI less than 30; understanding the Persian language; having literacy; absence of major psychiatric disorder; absence of other diseases such as neurological and musculoskeletal system disorders, cancer, not heart attack or angina attack in last month; having established a treatment plan. Exclusion criteria: Admission in hospital during of study; patient required to oxygen or spray during of six minute walking test; absence of patient in group educational session; impossibility for follow up.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Dyspnea. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Borg Scale.;Exercise Tolerance. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Six Minutes Walking Test.;Pumonary Function. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Spirometery Test.;Fatigue. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Fatigue Sever Scale.	—

Measure

Time frame

Dyspnea. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Borg Scale.;Exercise Tolerance. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Six Minutes Walking Test.;Pumonary Function. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Spirometery Test.;Fatigue. Timepoint: befor the intervention, 12 weeks after intervention. Method of measurement: Fatigue Sever Scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Heidari

Ahvaz Jondishapor University of Medical Science

heidari.ma@ajums.ac.ir; heidari.maryam84@yahoo.com+98 61 1373 2422

Outcome results

None listed

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