NCT01936428

Brief 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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2013

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2013

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2013

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

August 27, 2013

Completed
10 days until next milestone

First Posted

Study publicly available on registry

September 6, 2013

Completed
Last Updated

October 1, 2015

Status Verified

September 1, 2015

Enrollment Period

4 months

First QC Date

August 27, 2013

Last Update Submit

September 29, 2015

Conditions

Palliative Care Perception

Outcome Measures

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

    1 day

Secondary Outcomes (1)

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

    1 day

Study Arms (1)

interview

OTHER
Other: interview

Interventions

interviewOTHER
interview

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Interviews as Topic

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 27, 2013

First Posted

September 6, 2013

Study Start

January 1, 2013

Primary Completion

May 1, 2013

Study Completion

May 1, 2013

Last Updated

October 1, 2015

Record last verified: 2015-09