- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06551831
End-of-life Decision-making Among Young Patients With Advanced Cancer: a Grounded Theory Approach
August 11, 2024 updated by: National Taiwan University Hospital
The purpose of this qualitative research is to use grounded theory to explore and describe the thoughts of young advanced cancer patients regarding end-of-life care and how these thoughts influence the related decision-making process.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Pei-Yu Hsu
- Phone Number: 267940 +886-23123456
- Email: 020854@ntuh.gov.tw
Study Locations
-
-
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Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Pei-Yu Hsu
- Phone Number: 267940 +886-23123456
- Email: 020854@ntuh.gov.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
- The patient has a solid tumor.
- The age at initial cancer diagnosis is between 15 and 39 years.
- The patient is at least 18 years old at the time of enrollment.
- The patient has cancer with metastasis, either present at initial diagnosis or occurring after treatment or follow-up.
- After metastasis, the first-line curative treatment is ineffective.
Description
Inclusion Criteria:
- The patient has a solid tumor.
- The age at initial cancer diagnosis is between 15 and 39 years.
- The patient is at least 18 years old at the time of enrollment.
- The patient has cancer with metastasis, either present at initial diagnosis or occurring after treatment or follow-up.
- After metastasis, the first-line curative treatment is ineffective.
Exclusion Criteria:
- Patients who, for any reason, including severe psychological distress (as determined by the attending physician, psychiatrist, or specialist nurse based on assessments and impressions during routine patient care), cognitive impairment, or physical limitations (such as frailty), are unable to communicate or participate in an interview lasting more than 30 minutes.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Young Patients With Advanced Cancer
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Interview Guide
Time Frame: 2024/7~2025/7
|
1.The journey since diagnosis.
2. The most profound or recent medical decision.
3. The most profound or recent medical decision.
4. Anticipated future medical decisions.
5. Future end-of-life care options
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2024/7~2025/7
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 23, 2024
Primary Completion (Estimated)
July 1, 2025
Study Completion (Estimated)
July 1, 2025
Study Registration Dates
First Submitted
August 4, 2024
First Submitted That Met QC Criteria
August 11, 2024
First Posted (Actual)
August 13, 2024
Study Record Updates
Last Update Posted (Actual)
August 13, 2024
Last Update Submitted That Met QC Criteria
August 11, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202406142RINE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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