- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00792896
Intervention Toward Truth-Telling and Advanced Directives in the Patient With Advanced or Metastatic Disease
November 17, 2008 updated by: National Taiwan University Hospital
A Longitudinal Study That Assessed the Effectiveness of Intervention Toward
Family usually had a lot of burden to tell the truth to patients.
The purpose of this study is to assess the effect of education materials and family conference for advanced cancer patients and family.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
150
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Hospital
-
Contact:
- We-Yu Hu, Ph.D
- Phone Number: 88428 23123456
- Email: weyuhu@ntu.edu.tw
-
Principal Investigator:
- We-Yu Hu, Ph.D
-
-
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
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- advanced or metastatic cancer patients
- more than 20 years old
- clear consciousness and be able to communicate
Exclusion Criteria:
- refuse to know the statement of himself/herself disease
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
- Primary Purpose: Health Services Research
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 1
Family conference + education materials
|
family conference
|
|
No Intervention: 2
education materials
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Questionnaires
Time Frame: before and 1 week after the intervention
|
before and 1 week after the intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
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
May 1, 2008
Primary Completion (Anticipated)
December 1, 2010
Study Registration Dates
First Submitted
November 16, 2008
First Submitted That Met QC Criteria
November 17, 2008
First Posted (Estimate)
November 18, 2008
Study Record Updates
Last Update Posted (Estimate)
November 18, 2008
Last Update Submitted That Met QC Criteria
November 17, 2008
Last Verified
May 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 200803051R
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.