- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06823505
Lung Cancer Patients and Parent-child Interaction Experience and Process
Type of study: The goal of this observational study is to explore the relationship between patients with advanced lung cancer and their parent-child interactions during the treatment process, and to understand the impact of the degree of self-differentiation of parents with advanced lung cancer on the physical and mental health of their children. The main questions it aims to answer are:
- To explore the post-illness adjustment process of patients with advanced lung cancer and the changes in the parent-child relationship among adolescents.
- To explore the changes in demographic factors-self-belief, mental health, and self-efficacy among patients with advanced lung cancer-and the parent-child relationship among adolescents.
- Explore the family resilience of patients with advanced lung cancer - family peer relationships, and the interaction between parent-child relationships among adolescents.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Taipei, Taiwan, 100225
- Nation Taiwan University Hospital
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Taipei City, Taiwan, 100225
- National Taiwan University Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with advanced lung cancer aged 40 to 64 years (mid-adulthood).
- There are lung cancer patients in the family who are teenagers aged 10 to 19 years old.
- Those who voluntarily participate in this study.
- Voluntary participants can express themselves orally and in handwriting.
Exclusion Criteria:
- Single lung cancer patients over 65 years old.
- Lung cancer patients under 40 years old.
- Patients diagnosed with early-stage lung cancer.
- Those who have cognitive impairment and are unable to understand the problem.
- Those who are unable to express and respond to questions.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parent-child interaction
Time Frame: one years
|
The interaction between patients with advanced lung cancer and their parents and children during the treatment process
|
one years
|
|
Center for Epidemiological Studies Depression Scale
Time Frame: one years
|
The CES-D scale is designed to measure an individual's depression level, covering multiple aspects such as depressed mood, guilt, helplessness, decreased appetite, sleep disturbance and psychomotor retardation, with a total of 20 items.
The subjects evaluated the frequency of each symptom in the past week using a four-point scale (1 point: never or rarely; 4 points: often).
Studies have shown that CES-D has good internal consistency (α=0.85)
(Conerly et al., 2002; Given et al., 2004) and reliability (Cronbach's alpha > 0.85) in cancer patients (Hann et al., 2004).
al., 1999) , and therefore can effectively assess the level of depression in cancer patients.
In short, the CES-D is a validated tool for assessing depression in cancer patients.
|
one years
|
Collaborators and Investigators
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
- 202306102RINB
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
product manufactured in and exported from the U.S.
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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