Prospective National Survey of the Palliative Situation Among Inmates in French Prisons (PARME)

February 23, 2015 updated by: Régis AUBRY, Centre Hospitalier Universitaire de Besancon

PARME study had 3 objectives:

  • To identify the specific number of incarcerated individuals with terminal illness in need of palliative care.
  • To describe the health and penal situation of these prisoners.
  • To analyse the situation of these ill prisoners especially in the context of suspended sentence for medical ground

In order to answer these questions, the investigators used a mixed method research.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

First, in order to establish a baseline, the investigators contacted the medical units in all French prisons, which means 178 care units and 8 secures inpatient care units. The investigators census every patient with terminal illness, which was defined in this study as an evolutive pathology with a life prognosis less than a year.

A questionnaire was completed by these physicians for every situation. The census was conducted for three months across France.

For the qualitative study, the investigators selected 14 specific situations chosen into these which had been identified by the physicians.

The investigators wanted to get 3 types of patients :

  1. patient who had obtained a compassionate release
  2. patient whose demand has been refused
  3. patient who did not demand any release. The four interviews (patients, physisians, judges, probation workers) for each situation has explained the global situation.

Each interviewee spoke about the situation with his/her perspective and sense that they attributed to the actions of others.

This research analyzes the particularity of each of these end of life situations in prison.

Study Type

Observational

Enrollment (Actual)

15

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Every prisonners with terminal illness

Description

Inclusion Criteria:

  • prisonners
  • serious and evolving pathology
  • vital prognosis less than a year

Exclusion Criteria:

  • less than 18 year
  • person under tutelage
  • patient who refuse to participate

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
census
qualitative interview
some patient are interviewed.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
census ill prisonners with vital prognosis less than a year and understand how penal and medical professional are coping with these situations
Time Frame: 1 year
1 year

Secondary Outcome Measures

Outcome Measure
Time Frame
uderstand how professionnels are coping with not condamned prisonners
Time Frame: 1 year
1 year
Question the meaning of the sentence for ill prisonners
Time Frame: 1 year
1 year
Compare the way professionnal are coping with these situation around France
Time Frame: 1 year
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Edouard Amzallag, Dr, CHU Lyon
  • Principal Investigator: Sebastien Grignard, Dr, Centre Hospitalier Universitaire de Besançon
  • Principal Investigator: Blanchet Emmanuelle, Dr, CHU Nancy
  • Principal Investigator: Grimopont Frederic, Dr, CHU Lille
  • Principal Investigator: Bartoli Christophe, Dr, CHU Marseille
  • Principal Investigator: BAYLE Paule, Dr, CHU Toulouse
  • Principal Investigator: Bedry Regis, Dr, CHU Bordeaux
  • Principal Investigator: Bernard Benoit, Dr, CHU Rennes
  • Principal Investigator: Auger Yvain, Dr, APHP

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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, 2011

Primary Completion (Actual)

October 1, 2013

Study Completion (Actual)

December 1, 2013

Study Registration Dates

First Submitted

February 9, 2015

First Submitted That Met QC Criteria

February 9, 2015

First Posted (Estimate)

February 12, 2015

Study Record Updates

Last Update Posted (Estimate)

February 24, 2015

Last Update Submitted That Met QC Criteria

February 23, 2015

Last Verified

February 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • 2011-A00791-40

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.

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