NCT00674037

Brief Summary

Patients' recruitment is difficult in clinical trial. Financial incentives are frequently proposed to clinicians in private funded trials. However, the effect of these financial incentives has never been evaluated. The purpose of this study is to evaluate the effect of financial incentive on the rate of recruitment of patients in a cohort study.

Trial Health

57
Monitor

Trial Health Score

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

Enrollment
170

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2006

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

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

September 1, 2006

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

April 9, 2008

Completed
28 days until next milestone

First Posted

Study publicly available on registry

May 7, 2008

Completed
3.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2011

Completed
Last Updated

November 3, 2014

Status Verified

December 1, 2013

Enrollment Period

5 years

First QC Date

April 9, 2008

Last Update Submit

October 31, 2014

Conditions

Keywords

recruitmentphysicians participating in the recruitment of patients

Outcome Measures

Primary Outcomes (1)

  • number of patient included

    3 months

Secondary Outcomes (1)

  • number of patient included

    6 month

Study Arms (2)

inclusion with financial motivation

EXPERIMENTAL

75 euros for each patient included

Other: monetary incentive

no incentive

NO INTERVENTION

no incentive

Interventions

75 euros for each patient included

inclusion with financial motivation

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Physicians participating in the COFRASA cohort study
  • informed consent

You may not qualify if:

  • \- None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Groupe hospitalier Bichat-Claude Bernard

Paris, 75018, France

Location

Study Officials

  • Isabelle BOUTRON, MD

    Assistance Publique - Hôpitaux de Paris

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 9, 2008

First Posted

May 7, 2008

Study Start

September 1, 2006

Primary Completion

September 1, 2011

Study Completion

September 1, 2011

Last Updated

November 3, 2014

Record last verified: 2013-12

Locations