The study's purpose is to understand the self-management needs of patients with NSCLC receiving targeted therapy, develop a disease self- management application (mHealth Application), and explore the effect of mHealth application on the self-efficacy and health status of patients receiving targeted therapy for NSCLC. This study adopts a two-group (pre-and-post-test) design experiment. This study is being conducted over a period of 3 years and is divided in two stages. This study enrolled patients with NSCLC in the outpatient clinic and ward of the Division of Chest Medicine in a northern medical center as the research participants. Stage 1 develop a disease self-management application and understands participants' needs by qualitative study. The participants are a purposive sample of 15-20 patients. Data discontinued when theme saturation is achieved. Stage 2 adopted convenient sampling to enroll 108 patients (54 in the experimental group and 54 in the control group) to evaluate the effectiveness of the disease self-management application. After participant's consent was obtained, this study performed the pre-test and randomized the participants. The experimental group received both routine care and the disease self-management App, while the control group received routine care and part of application. This study collected data before the patients received targeted therapy and in months 1, 3, 6, and 9 after treatment initiation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Enrollment
108
The mHealth application provide disease self-management knowledge and skills and also has the functions of level of skin toxicity warning, uploading photos of skin toxicity, and interacting with healthcare professionals.
European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire
assessing participants' quality of life
Time frame: change from baseline at 1 month
European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire
assessing participants' quality of life
Time frame: change from baseline at 3 month
European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire
assessing participants' quality of life
Time frame: change from baseline at 6 month
European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire
assessing participants' quality of life
Time frame: change from baseline at 9 month
NCI-CTCAE (ver 5.0) guideline
assessing participants' skin toxicity grade
Time frame: change from baseline at 1 month
NCI-CTCAE (ver 5.0) guideline
assessing participants' skin toxicity grade
Time frame: change from baseline at 3 month
NCI-CTCAE (ver 5.0) guideline
assessing participants' skin toxicity grade
Time frame: change from baseline at 6 month
NCI-CTCAE (ver 5.0) guideline
assessing participants' skin toxicity grade
Time frame: change from baseline at 9 month
knowledge and skills with disease self-management questionnaire
assessing participants' knowledge and skill ability with disease self-management
Time frame: change from baseline at 1 month
knowledge and skills with disease self-management questionnaire
assessing participants' knowledge and skill ability with disease self-management
Time frame: change from baseline at 3 month
knowledge and skills with disease self-management questionnaire
assessing participants' knowledge and skill ability with disease self-management
Time frame: change from baseline at 6 month
knowledge and skills with disease self-management questionnaire
assessing participants' knowledge and skill ability with disease self-management
Time frame: change from baseline at 9 month
disease self-efficacy questionnaire
assessing participants' self-efficacy with disease self-management
Time frame: change from baseline at 1 month
disease self-efficacy questionnaire
assessing participants' self-efficacy with disease self-management
Time frame: change from baseline at 3 month
disease self-efficacy questionnaire
assessing participants' self-efficacy with disease self-management
Time frame: change from baseline at 6 month
disease self-efficacy questionnaire
assessing participants' self-efficacy with disease self-management
Time frame: change from baseline at 9 month
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Hospital Anxiety and Depression Scale
assessing participants' anxiety and depression
Time frame: change from baseline at 1 month
Hospital Anxiety and Depression Scale
assessing participants' anxiety and depression
Time frame: change from baseline at 3 month
Hospital Anxiety and Depression Scale
assessing participants' anxiety and depression
Time frame: change from baseline at 6 month
Hospital Anxiety and Depression Scale
assessing participants' anxiety and depression
Time frame: change from baseline at 9 month
Medical Outcomes Study-Social Support Survey
assessing participants' social support
Time frame: chang from baseline at 1 month
Medical Outcomes Study-Social Support Survey
assessing participants' social support
Time frame: chang from baseline at 3 month
Medical Outcomes Study-Social Support Survey
assessing participants' social support
Time frame: chang from baseline at 6 month
Medical Outcomes Study-Social Support Survey
assessing participants' social support
Time frame: chang from baseline at 9 month