NCT02915653

Brief Summary

The study is a pre-post two round, randomized controlled study design of PCPs randomly assigned to a control or 1 of 2 intervention arms.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
213

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Sep 2016

Geographic Reach
1 country

1 active site

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

September 1, 2016

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

September 22, 2016

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 27, 2016

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2016

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2017

Completed
Last Updated

June 20, 2018

Status Verified

June 1, 2018

Enrollment Period

2 months

First QC Date

September 22, 2016

Last Update Submit

June 18, 2018

Conditions

Preventive Care

Outcome Measures

Primary Outcomes (1)

  • Quality of Care

    Difference in difference of combined diagnostic and treatment CPV domain scores, including colonoscopy referral rates, in post-intervention versus baseline comparing intervention and control groups among the three patient types.

    8 weeks

Secondary Outcomes (3)

  • Intervention Impact on Care

    8 weeks

  • Healthcare Utilization

    8 weeks

  • Diagnostic Method Comparison

    8 weeks

Study Arms (3)

Control

NO INTERVENTION

Control: not receiving any intervention

Intervention 1

EXPERIMENTAL

Receiving educational materials on a new diagnostic service

Other: Educational materials on a new diagnostic service

Intervention 2

EXPERIMENTAL

Receiving educational materials on a new diagnostic service

Other: Educational materials on a new diagnostic service

Interventions

Educational materials on a new diagnostic serviceOTHER

Educational materials on a new diagnostic service

Intervention 1Intervention 2

Eligibility Criteria

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

You may qualify if:

  • \. Provide consent to participate in the study 2. Board-certified physician currently practicing in the following areas: 3. Internal medicine 4. Family medicine 5. Have practiced as a board-certified physician in internal or family medicine for greater than 2 but less than 30 years. 6. English-speaking 7. Community / non-academic based practice setting 8. ≥ 40 patients under care weekly 9. Access to the internet

You may not qualify if:

  • \. Not board certified in their respective area of care 2. Academic-based practice 3. Have practiced as a board-certified physician for less than 2 or greater than 30 years 4. Follow \<40 patients weekly 5. Non-English speaking 6. Unable to access the internet

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

QURE Healthcare

San Francisco, California, 94109, United States

Location

Study Officials

  • John Peabody, MD, PhD

    QURE Healthcare

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
CARE PROVIDER
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 22, 2016

First Posted

September 27, 2016

Study Start

September 1, 2016

Primary Completion

November 1, 2016

Study Completion

November 1, 2017

Last Updated

June 20, 2018

Record last verified: 2018-06

Data Sharing

IPD Sharing
Will not share

Locations

US(1)