Chronic obstructive pulmonary disease. Other chronic obstructive pulmonary disease
Conditions
Interventions
Intervention 1: Intervention group:In the intervention group, instruction based on educational pictograms, which included information related to disease management, improving sleep quality, and increa
Sponsors
Shahre-kord University of Medical Sciences
Eligibility
Sex/Gender
All
Age
45 Years to 75 Years
Inclusion criteria
Inclusion criteria: .Definite diagnosis of chronic obstructive pulmonary disease (COPD) by the treating physician. Ability to speak Persian Patients in stages 2 and 3 of the disease according to the GOLD classification Absence of life-threatening diseases Voluntary consent to participate in the study Age between 45 and 70 years Ability to understand and respond to educational pictograms Ability to understand pictograms through the Pictogram Comprehension Test: In this test, patients are presented with several standard pictograms and asked to explain the meaning and concept of each image. The patients' responses are compared with a standard checklist and if the individual correctly identifies at least 70% of the concepts, they are considered to have the ability to understand pictograms Not having mental, motor, visual, or hearing disabilities
Exclusion criteria
Exclusion criteria: History of psychological problems Blindness, deafness, or speechlessness Being in another clinical trial Isolated patients who are in quarantine conditions Patients with motor disabilities Unknown patients who do not have correct identification details Patients with drug addiction
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep quality. Timepoint: Before the intervention_Immediately after the intervention_3 months after the intervention. Method of measurement: Pittsburgh Sleep Quality Questionnaire.;Activity tolerance. Timepoint: Before the intervention_Immediately after the intervention_3 months after the intervention. Method of measurement: 6-minute walk test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Decreased time to fall asleep. Timepoint: Before the start of the intervention - Immediately after the end of the intervention - 3 months after the end of the intervention. Method of measurement: Pittsburgh Sleep Quality Questionnaire.;Reduction in nighttime awakenings. Timepoint: Before the start of the intervention - Immediately after the end of the intervention - 3 months after the end of the intervention. Method of measurement: Pittsburgh Sleep Quality Questionnaire.;Feeling refreshed and energetic in the morning. Timepoint: Before the start of the intervention - Immediately after the end of the intervention - 3 months after the end of the intervention. Method of measurement: Pittsburgh Sleep Quality Questionnaire.;Increased distance covered in the 6-minute walk test. Timepoint: Before the start of the intervention - Immediately after the end of the intervention - 3 months after the end of the intervention. Method of measurement: 6-minute walk test.;Improve activity time. Timepoint: Before the start of the intervention - Immediately after the end of the intervention - 3 months after the end of the intervention. Method of measurement: 6-minute walk test.;Reduce the need to rest during walks. Timepoint: Before the start of the intervention - Immediately after the end of the intervention - 3 months after the end of the intervention. Method of measurement: 6-minute walk test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Rafi Boldaji
Shahre-kord University of Medical Sciences
Outcome results
None listed