Effect of Mobile Application-Based Education on Self-Efficacy, Medication Adherence and Sleep Quality in Asthma.
NCT ID: NCT07139080
Last Updated: 2025-08-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
68 participants
INTERVENTIONAL
2023-12-01
2025-04-28
Brief Summary
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The AstımAsistan application was designed to monitor changes in patient self-efficacy, medication adherence, and sleep quality through three core features: (1) patient education modules, (2) breathing exercise/medication reminders, and (3) mobile consultation capabilities.
Study data were collected using four instruments: (1) the Participant Information Form, (2) the Chronic Disease Self-Efficacy Scale, (3) the Medication Adherence Reporting Scale, and (4) the Pittsburgh Sleep Quality Index. The mobile education-based application was developed following the ADDIE (Analysis, Design, Development, Implementation, and Evaluation) instructional design model."
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Mobile Education Group
It consists of participants who will download the mobile patient education and breathing exercise reminder program and apply it for 10 weeks.
Mobile education
It consists of participants who will download the mobile patient education and breathing exercise reminder program and apply it for 10 weeks.
Control Group
This is the group of participants to be followed within the standard treatment plan. A mobile training and breathing exercise reminder program will be downloaded to patients in this group at the end of the study.
No interventions assigned to this group
Interventions
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Mobile education
It consists of participants who will download the mobile patient education and breathing exercise reminder program and apply it for 10 weeks.
Eligibility Criteria
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Inclusion Criteria
2. Having been diagnosed with asthma at least 6 months ago
3. Being treated for asthma in oral, inhaler or injection forms
4. Being literate in Turkish
5. Having an Android phone on which the mobile application can be installed and being able to use the phone
6. Having mobile network or wireless internet access
7. Volunteering to participate in research
8. Living in Ankara
Exclusion Criteria
2. Having a language barrier that hinders communication
3. Being diagnosed with COPD
4. Being diagnosed with a psychiatric disease
5. Being on psychoactive or opioid therapy
6. Being diagnosed with a sleep disorder related to non-respiratory reasons (physical and psychological) and being treated
Intervention group;
1. The participant was diagnosed with a health problem requiring inpatient treatment during the study period.
2. The participant withdraws from the study voluntarily.
3. Inability to use the mobile application during the research
4. Reading fewer than 6 theme headings in the mobile application (75% or less) and missing breathing exercises for more than 16 days (80% or less)
Control group;
1. The participant was diagnosed with a health problem requiring inpatient treatment during the study period.
2. The participant withdraws from the study voluntarily.
18 Years
65 Years
ALL
No
Sponsors
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Gulhane Training and Research Hospital
OTHER_GOV
Responsible Party
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Ezgi Yildirim
Principal İnvestigator
Principal Investigators
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AYLA DEMİRTAŞ, Associate Professor
Role: STUDY_DIRECTOR
UNIVERSITY OF HEALTH SCIENCES GULHANE FACULTY OF NURSING
Locations
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Gulhane Training and Research Hospital
Ankara, KEÇİÖREN, Turkey (Türkiye)
Countries
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Other Identifiers
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Asthma Mobil Nursing Education
Identifier Type: -
Identifier Source: org_study_id
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