Staff Opinions and Knowledge Concerning Organ and Tissue Harvesting: an Investigation Among the Patient Care Personnel in the South-Mediterranean Region of France

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier Universitaire de Nīmes
ClinicalTrials.gov Identifier:
NCT01213069
First received: September 30, 2010
Last updated: March 3, 2014
Last verified: March 2014
  Purpose

The goal of this study is to evaluate the knowledge of paramedical and medical care personnel concerning organ and tissue donations, as well as their opinions on this activity.


Condition Intervention
Tissue and Organ Procurement
Other: Questionnaires

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Staff Opinions and Knowledge Concerning Organ and Tissue Harvesting: an Investigation Among the Patient Care Personnel in the South-Mediterranean Region of France

Further study details as provided by Centre Hospitalier Universitaire de Nīmes:

Primary Outcome Measures:
  • VAS Negative/positive feeling [ Time Frame: 1 day ] [ Designated as safety issue: No ]
    Visual Analog Scale from 0 to 100 where 0 is negative and 100 is positive.


Enrollment: 1859
Study Start Date: March 2010
Study Completion Date: July 2012
Primary Completion Date: July 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
all 5000 subjects
this is a purely descriptive study with one group
Other: Questionnaires
The subjects are asked to fill out a questionnaire on the personal and professional situations, organ donation legislation, what happens in everyday practice, their own experience with donating their own organs, and what position they take.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Health care personnel in South-Mediterranean France

Criteria

Inclusion Criteria:

  • paramedical or medical care personnel from a participating center
  • participates in organ donor activities
  • works in a department with organ donor activity

Exclusion Criteria:

  • personnel with no contact with organ donor activities
  • personnel from non-participating centers
  • refuses to participate
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01213069

Locations
France
AP-HM Hôpital Nord
Marseille, France, 13915
Hôpital Guy de Chauliac, CHU de Montpellier
Montpellier Cedex 05, France, 34295
Hôpital Cimiez, CHU de Nice
Nice, France, 06003
Centre Hospitalier Universitaire de Nîmes
Nimes, France, 30029
Sponsors and Collaborators
Centre Hospitalier Universitaire de Nīmes
Investigators
Principal Investigator: Caroline Boutin, MD Centre Hospitalier Universitaire de Nîmes
  More Information

No publications provided

Responsible Party: Centre Hospitalier Universitaire de Nīmes
ClinicalTrials.gov Identifier: NCT01213069     History of Changes
Other Study ID Numbers: PHRC-I/2009/CB-01, 1391089
Study First Received: September 30, 2010
Last Updated: March 3, 2014
Health Authority: France: The Commission nationale de l’informatique et des libertés

ClinicalTrials.gov processed this record on August 20, 2014