Bernese Next of Kin Survey Following Organ Donation Request

August 29, 2018 updated by: Andreas Bloch, University Hospital Inselspital, Berne

Next of Kin Survey Following Organ Donation Request - a Single Center Experience

6 to 18 months after organ donation request a next of kin survey using a standardized questionnaire was conducted.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

117

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Switzerland
      • Bern, Switzerland, 3010
        • Department for Intensive Care Medicine

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

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Next of kin involved in request for organ donation. Single center study. The request for organ donation must have passed 6 to 18 months ago

Description

Inclusion Criteria:

Next of kin involved in request for organ donation

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
request for organ donation approved
Behavioral: questionnaire
a standardized questionnaire was sent to all participants
request for organ donation rejected
Behavioral: questionnaire
a standardized questionnaire was sent to all participants

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
factors influencing approval/rejection of an organ donation
Time Frame: 6 to 18 months pre questionnaire
6 to 18 months pre questionnaire
factors with influence on mourning porcess
Time Frame: 6 to 18 months past request
6 to 18 months past request

Collaborators and Investigators

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

Sponsor

University Hospital Inselspital, Berne

Investigators

  • Principal Investigator: Andreas Bloch, MD, department of critical care medicine, inselspital, university hospital, bern, university of bern

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 (ACTUAL)

March 1, 2018

Primary Completion (ACTUAL)

July 1, 2018

Study Completion (ACTUAL)

July 24, 2018

Study Registration Dates

First Submitted

July 24, 2018

First Submitted That Met QC Criteria

July 25, 2018

First Posted (ACTUAL)

August 2, 2018

Study Record Updates

Last Update Posted (ACTUAL)

August 31, 2018

Last Update Submitted That Met QC Criteria

August 29, 2018

Last Verified

August 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • BNoKSurvey FODR

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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