- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02903953
Clinical Research Outside of Teaching Hospitals (RECHNONU) (RECHNONU)
Clinical Research Outside of Teaching Hospitals : Current Situation in North-eastern France
Study Overview
Status
Conditions
Detailed Description
The very most part of clinical research in France takes place in teaching hospitals. Advantages to develop it in others hospitals are numerous: access to innovative treatments, improvement of healthcare quality, hospitals' attractiveness, increased inclusion rates and reduced selection bias. The objective the study is report the current situation of clinical research outside of teaching hospitals in France.
A three-stage survey was conducted between January and October 2012 in non-teaching hospitals of North-eastern France. First questionnaires were sent to administrative and medical boards of all hospitals with more than 100 beds, then to head doctors of every department in hospitals with more than 300 beds and finally meetings were organized with clinical research actors of 20 selected hospitals.
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- non-teaching hospitals
- established in north-eastern France
Exclusion Criteria:
- more than 100 beds
- for the second stage only:
- less than 300 beds
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Description of the clinical research in non-teaching hospitals of north-eastern France
Time Frame: 1 year
|
Self-Assessment Questionnaire
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Specificities of each centers in clinical research
Time Frame: 1 year
|
Self-Assessment Questionnaire
|
1 year
|
Problems to solve for developing clinical research
Time Frame: 1 year
|
semi-structured interview
|
1 year
|
Collaborators and Investigators
Investigators
- Study Director: Christophe GOETZ, MD, CHR Metz-Thionville
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2012-01Obs-CHRMT
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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