ClinicalTrials.gg
CompletedNCT01936428Updated Oct 1, 2015

Prospective Study of the Perception of Palliative Care by Relatives of Patients Treated in Oncology

An interventional study of interview in Palliative Care Perception, sponsored by Hospices Civils de Lyon. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-10-01.

Sponsored by Hospices Civils de Lyon · Not applicable and Interventional

Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate (thanks to analysed interview) the perception of palliative care by relatives of patients treated in oncology.

02

Conditions studied

  • Palliative Care Perception
03

In context

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,856 studies on the registry; 442 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • man or woman of age who is a relative of a patient treated in oncology
  • subject who signed the informed consent
  • subject without any legal protection measure and having health coverage

Exclusion criteria

Exclusion Criteria:

  • Relatives of patients already followed in the palliative care departement
  • Subjects with cognitive impairment or expression;
  • Not french spoken subjects
  • Pregnant or breastfeeding women
05

Study design

Phase
Not applicable
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Other
    interview

    Other: interview

Interventions

  • Otherinterview
06

What researchers measure

Primary outcomes

  1. Perception of palliative care evaluated by an interview with the investigator

    The interview takes place the same day the subject signs the informed consent ; it lasts around 1 hour

    Time frame: 1 day

Secondary outcomes

  1. analysis of main elements to be used in the early information to patients and their families about palliative care.

    Time frame: 1 day

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 1, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01936428
Responsible party
Sponsor
First posted
Sep 6, 2013
Start date
Jan 2013
Primary completion
May 2013
Completion
May 2013
Last update
Oct 1, 2015

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2015. You cannot join it, but the record below documents what was studied.

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