- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07419906
Effect of Introducing Digital Multimedia Nursing on Improving With COPD (COPD)
Effect of Introducing Transtheory-based Digital Multimedia Nursing and Health Education Model on Improving the Self-Care of Older Adult Patients With Chronic Obstructive Pulmonary Disease
Study Overview
Status
Intervention / Treatment
Detailed Description
COPD is a chronic and progressive respiratory disease characterized by persistent airflow limitation and symptoms such as dyspnea, chronic cough, and sputum production. The disease significantly impairs daily functioning and quality of life, particularly among older adults. Despite its high prevalence, COPD remains underdiagnosed and inadequately managed in Taiwan.
To improve disease management, digital health education strategies may enhance patients' knowledge and self-care abilities. This study aims to evaluate the effectiveness of a transtheoretical model-based digital multimedia nursing education intervention in improving disease knowledge, self-management behaviors, and quality of life among elderly patients with COPD.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Taiwan
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New Taipei City, Taiwan, Taiwan, 243
- Taiwan
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients diagnosed with pulmonary obstruction after evaluation by a physician.
- Elderly people aged 60 years or above.
- Those who are literate, have clear consciousness and can communicate in Chinese and Taiwanese.
- Those who agree to participate in this research and sign the consent form.
Exclusion Criteria:
- Patients with respiratory distress syndrome.
- Those who use respirators.
- Those who are unable to communicate due to cognitive impairment due to major mental illness or dementia.
- Color blindness and visual impairment.
- Those who do not have mobile phones or tablet computers at home and cannot obtain electronic equipment.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: E-book on Pulmonary Obstruction
A experimental design was adopted.
Simple random sampling was performed to divide the subjects into the traditional teaching material-based intervention group and digital teaching material-based intervention group.
A total of 51 patients with COPD and aged ≥60 years were recruited from the outpatient department of a hospital in northern Taiwan.
The two groups respectively received health education through traditional paper teaching materials and digital multimedia teaching materials; 50-minute interventions were conducted once per week for 8 weeks, and measurements were taken before the interventio, 8 and 12 weeks after the intervention.
Regarding the performance indicators, a paired t test and generalized estimating equation (GEE) were used to analyse differences in the COPD Assessment Test (CAT)、self-care efficiency scale for COPD and COPD knowledge scale.
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The digital teaching intervention group used a computer-downloaded "E-book on Pulmonary Obstruction" for one-on-one teaching.
The subjects were also taught how to use their mobile phones to download the "E-book on Pulmonary Obstruction" and how to read it, so that they could use it on their own after returning home.
The intervention time for both groups was once a week for 50 minutes each time for a total of 8 weeks.
The teaching content is divided into eight themes: (1) How much do you know about pulmonary obstruction?
(2) Inhalation treatment for pulmonary obstruction - Introduction to inhalers?
(3) Care for pulmonary obstruction - Breathing exercise techniques?
(4) Activities and exercise training?
(5) Self-management methods for acute pulmonary obstruction?
(6) Lung rehabilitation for pulmonary obstruction?
(7) Nutritional care for pulmonary obstruction?
(8) Care for pulmonary obstruction - Smoking cessation?
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No Intervention: The traditional teaching material-based group
The traditional teaching intervention group used the same health education content of the "E-book on Pulmonary Obstruction" printed into a paper manual for one-on-one teaching, and the same instructor provided health education guidance.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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COPD assessment test; CAT
Time Frame: Baseline (Week 1), Week 8, and Week 12
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The CAT is an 8-item questionnaire assessing the impact of COPD on health status and daily functioning.
Higher scores indicate greater disease burden.
This study evaluates the effectiveness of a digital multimedia nursing education intervention in improving disease knowledge, self-care, and self-management.
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Baseline (Week 1), Week 8, and Week 12
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Knowledge of COPD Score
Time Frame: Baseline (Week 1), Week 8, and Week 12
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Assessed using a validated COPD knowledge questionnaire to evaluate participants' understanding of disease management and self-care principles.
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Baseline (Week 1), Week 8, and Week 12
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Self-Care Behavior Score
Time Frame: Baseline (Week 1), Week 8, and Week 12
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Measured using a self-care behavior scale adapted for COPD, evaluating adherence to recommended lifestyle and symptom management strategies.
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Baseline (Week 1), Week 8, and Week 12
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Collaborators and Investigators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FuJenCUH
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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