Evaluation of the Effect of Web-designed Training Developed for Asthma Patients

Eskisehir Osmangazi University

Status: Completed

Conditions: Asthma

Treatments: Behavioral: EDUCATION

Study type: Interventional

Funder types: Other

Identifiers

NCT04607681

Eskisehir Osmangazi Universty

Details and patient eligibility

About

The study is an experimental study with pre-test-post-test control group in order to determine the effect of web-designed training developed for asthma patients on drug compliance, asthma control, and fatigue

Full description

In the first stage, it is aimed to develop, implement and evaluate a web designed asthma education program for asthma patients. In the second stage, it is to evaluate the effect of the web-designed education program developed for asthmatic patients on drug ompliance, asthma control, and fatigue The population of the study consists of patients diagnosed with asthma who are registered in Family Health Centers in Eskişehir. The individuals that constitute the target group in the study will be determined through the records of patients diagnosed with asthma registered in the family health center or the list of patients in the J45-Asthma and J46 Status Asthmaticus ICD codes. The sample of the study will be the patients who meet the criteria for inclusion in the study. G power analysis program was used to determine the sample size. The research will be conducted in two groups, an intervention and a control group. The sample size of the research was found to be 200.

In collecting research data; The personal descriptive characteristics form prepared by the researcher, the questionnaire for determining the information needs, Form for evaluation of the skills of using inhalation devices and the opinion form regarding the web-based asthma education program will be used. At the same time, COPD and asthma fatigue scale, drug compliance reporting scale and Asthma Control Test (AKT) will be used.

Enrollment: 200 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• 18 years and over,
• Those who have been diagnosed with asthma for at least one year
• Those with poor asthma control
• Using at least one asthma medication
• Not having a communication problem, such as inability to understand/speak Turkish, that would prevent participating in the research or receiving training,
• Being literate,
• Having an internet connection at home or on their phone,
• Having and using a computer, tablet or smart phone,
• Patients who accepted to participate in the study voluntarily formed the sample of the study.

Exclusion criteria

• No internet connection at home or on their phone,
• Do not know how to use the Internet and computer,
• Having a communication problem, such as inability to understand/speak Turkish, that would prevent participating in the research or receiving training,
• Illiterate,
• Diagnosed with another respiratory system disease,
• Diagnosed with cancer or undergoing cancer treatment,
• Those who have been diagnosed with or have had COVID-19,
• Individuals with a psychiatric illness were not included in the study.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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200 participants in 2 patient groups

1 GROUP

Experimental group

Description:

Patients who agree to participate in the study will be informed about the study and their written and verbal consent will be obtained. At this stage, which will last 6 weeks for each patient; * On the first day, the patients will be evaluated first by filling the "Individual Descriptive Features Form, Information Need Determination Question Form, COPD and Asthma Fatigue Scale, Medication Compliance Notification Scale, Asthma Control Test (ACT), Form for evaluation of the skills of using inhalation devices", * In order for the patients in the intervention group to use the web-based asthma education program, a web-based asthma education program will be introduced by giving their username and password. After 6 weeks of training, second data will be collected on the web in the intervention group.

Treatment:

Behavioral: EDUCATION

2 GROUP

No Intervention group

Description:

Written and verbal consents will be obtained from patients who agree to participate in the study by providing information about the study. At this stage, which will take 6 weeks for each patient; On the first day, the patients will first be evaluated by filling the "Individual Descriptive Characteristics Form, Information Requirement Determination Question Form, COPD and Asthma Fatigue Scale, Medication Compliance Notification Scale, Asthma Control Test (ACT), Form for evaluation of the skills of using inhalation devices", Second data after 6 weeks will be collected in the control group via Google form or phone call