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Palliative Care PerceptionNCT01936428

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

A study testing interview in people with Palliative Care Perception, run by Hospices Civils de Lyon.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Palliative Care Perception
What is being tested?
interview
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
No sites listed yet
Study dates
Jan 2013to May 2013
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

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

About this study

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

Being tested
interview

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • interviewOther

Study groups in NCT01936428
Study groupRoleWhat they receive
interviewOtherNot described
Receives: Other: interview

What is being measured

The primary outcome is the main question the study is designed to answer.

  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

    Measured: 1 day

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

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Sep 2013 (estimated)
  2. Study startJan 2013
  3. Primary completionMay 2013
  4. Study completionMay 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01936428
Sponsor's protocol ID
2012.743
Status last verified
Sep 2015
First submitted
27 Aug 2013
Last updated
1 Oct 2015
Results posted
No
Data monitoring committee
Yes

Questions about this trial

What is this clinical trial studying?

A study testing interview in people with Palliative Care Perception, run by Hospices Civils de Lyon.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Oct 2015. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Perception of palliative care evaluated by an interview with the investigator (time frame: 1 day). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Oct 2015.

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