NCT02903953

Brief Summary

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 objectives of the study are to report the current situation of clinical research outside of teaching hospitals in France.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
129

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2012

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2012

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2013

Completed
3.3 years until next milestone

First Submitted

Initial submission to the registry

August 26, 2016

Completed
21 days until next milestone

First Posted

Study publicly available on registry

September 16, 2016

Completed
Last Updated

September 16, 2016

Status Verified

August 1, 2016

Enrollment Period

1.3 years

First QC Date

August 26, 2016

Last Update Submit

September 13, 2016

Conditions

Medical Staff, Hospital

Outcome Measures

Primary Outcomes (1)

  • Description of the clinical research in non-teaching hospitals of north-eastern France

    Self-Assessment Questionnaire

    1 year

Secondary Outcomes (2)

  • Specificities of each centers in clinical research

    1 year

  • Problems to solve for developing clinical research

    1 year

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Non-teaching hospitals of North-eastern France

You may qualify if:

  • non-teaching hospitals
  • established in north-eastern France

You may not qualify if:

  • more than 100 beds
  • for the second stage only:
  • less than 300 beds

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Christophe GOETZ, MD

    CHR Metz-Thionville

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 26, 2016

First Posted

September 16, 2016

Study Start

January 1, 2012

Primary Completion

May 1, 2013

Study Completion

May 1, 2013

Last Updated

September 16, 2016

Record last verified: 2016-08

Data Sharing

IPD Sharing
Will not share