An observational study in Advance Directives, Oncology and Skin Cancer, sponsored by Central Hospital, Nancy, France. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-01-30.
Sponsored by Central Hospital, Nancy, France · Observational
The law about advance directives is evolving but, in France, few people write it.
Te main endpoint of this research is to estimate the proportion of patients who have written their advance directives or considering doing so in onco-dermatologic population. If this rate remains low, some insights on the reasons will be able to be advanced looking at the point of view and opinion of patients about this topic.
Seconds endpoints are :
For patients against or not planning to write it, understand their reasons
Estimate the proportion of patients requesting information and understand how they would like to receive it.
Investigate a possible association between the stage of the oncological disease and the positioning of the patient concerning advance directives.
6,741 studies on the registry are indexed under Carcinoma; 1,161 are open to participants now.
This study's planned enrollment of 150 is close to the median of 149 across 1,175 observational studies indexed under Carcinoma.
Browse Carcinoma studies →Central Hospital, Nancy, France is the lead sponsor of 778 studies on the registry; 183 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Cf beyond
> 18 ya
With one of the diagnoses below:
Exclusion Criteria:
Patients not in possession of all of its cognitive abilities Patients who can't read patients who don't speak french
patients with a skin lymphoma OR melanoma OR advanced skin squamous cell carcinoma OR advanced basal cell carcinoma accepting to answer to the anonymous survey
Other: no intervention, only complete a survey
we will ask patients to answer to a survey
Writing by the patient of its advance directives
Writing by the patient of his advance directves and, if not writing, positioning of the patient (rather favorable or rather unfavorable) as to the writing of his advance directives.
Time frame: when the patient complete the survey
reason for not writing advance directives
In patients who have not written their advance directives: reason for not writing the advance directives.
Time frame: when the patient complete the survey
Patient wishing to be more informed about the adavance directives during its management and, if so, by what means.
Time frame: when the patient complete the survey
Plan to share: No
No publications or documents are linked to this record.
This study is status unknown, as verified in Jan 2019. You cannot join it, but the record below documents what was studied.
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Central Hospital, Nancy, France