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

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

Study Locations

      • Taipei, Taiwan, 100
        • Recruiting
        • National Taiwan University Hospital
        • Contact:

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
Young Patients With Advanced Cancer
  1. The patient has a solid tumor.
  2. The age at initial cancer diagnosis is between 15 and 39 years.
  3. The patient is at least 18 years old at the time of enrollment.
  4. The patient has cancer with metastasis, either present at initial diagnosis or occurring after treatment or follow-up.
  5. After metastasis, the first-line curative treatment is ineffective.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
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

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.

Clinical Trials on End-of-life Decision-making

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