NCT00161460

Brief Summary

The purpose of this study is to determine if a prototype colorectal cancer screening program with the services of a cancer prevention specialist will increase utilization of appropriate colorectal cancer screening tests.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
80

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2005

Typical duration for not_applicable

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

June 1, 2005

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

September 8, 2005

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 12, 2005

Completed
2.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2008

Completed
Last Updated

May 13, 2016

Status Verified

May 1, 2016

Enrollment Period

3 years

First QC Date

September 8, 2005

Last Update Submit

May 11, 2016

Conditions

Keywords

Colorectal cancerMass screening

Outcome Measures

Primary Outcomes (1)

  • Colorectal cancer screening test utilization

    6 months

Secondary Outcomes (2)

  • Knowledge about colorectal cancer screening tests

    2 months

  • Cancer worry score

    2 months

Study Arms (2)

1

ACTIVE COMPARATOR

Study nurse contacts subjects who enroll in the intervention to provide detailed education about screening tests, to assess their risk for colorectal cancer, and to facilitate screening.

Behavioral: colorectal cancer screening intervention

2

NO INTERVENTION

Patients who do not enroll receive usual care from their primary care providers.

Interventions

Enrolled subjects receive tailored education from a registered nurse who also facilitates ordering and completion of screening tests

1

Eligibility Criteria

Age50 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age 50 years and over, enrolled for medical care in the UWPN clinics

You may not qualify if:

  • Primary care physicians feel they would not benefit from colorectal cancer screening, unwilling or unable to complete study procedures

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Washington

Seattle, Washington, 98195, United States

Location

MeSH Terms

Conditions

Colorectal Neoplasms

Condition Hierarchy (Ancestors)

Intestinal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsDigestive System DiseasesGastrointestinal DiseasesColonic DiseasesIntestinal DiseasesRectal Diseases

Study Officials

  • Cynthia Ko, MD

    University of Washington

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

September 8, 2005

First Posted

September 12, 2005

Study Start

June 1, 2005

Primary Completion

June 1, 2008

Study Completion

June 1, 2008

Last Updated

May 13, 2016

Record last verified: 2016-05

Locations