NCT01116960

Brief Summary

The investigators hypothesize that common objections to P4P relate to potential loss of autonomy or concerns about adverse effects on patient care.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Apr 2007

Typical duration for all trials

Geographic Reach
1 country

2 active sites

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

April 1, 2007

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2010

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

May 3, 2010

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 5, 2010

Completed
Last Updated

May 4, 2017

Status Verified

May 1, 2017

Enrollment Period

2.9 years

First QC Date

May 3, 2010

Last Update Submit

May 1, 2017

Conditions

Keywords

P4P

Study Arms (3)

Faculty; MD

Full time Faculty members working with the Department

CRNAs

Full time CRNAs working within the department

Residents

Residents working within the department

Eligibility Criteria

Age24 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

anesthesia care providers

You may qualify if:

  • All anesthesia care providers in the department

You may not qualify if:

  • locum faculty members and CRNAs

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Univeristy of Oklahoma Health Sciences Center Dept. Anesthesiology

Oklahoma City, Oklahoma, 73104, United States

Location

Univeristy of Oklahoma Health Sciences Center

Oklahoma City, Oklahoma, 73104, United States

Location

MeSH Terms

Conditions

Behavior

Study Officials

  • Pamela Roberts, MD

    University of Oklahoma

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

May 3, 2010

First Posted

May 5, 2010

Study Start

April 1, 2007

Primary Completion

March 1, 2010

Study Completion

March 1, 2010

Last Updated

May 4, 2017

Record last verified: 2017-05

Data Sharing

IPD Sharing
Will not share

Locations