NCT00269009

Brief Summary

The investigators want to find out if providing a Community Health Educator Referral Liaison (CHERL) helps practices help their patients change risky behaviors (tobacco use, physical inactivity, unhealthy diet, and risky drinking) by connecting patients to available services in the community or directly providing behavior change support.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Timeline
Completed

Started Jan 2006

Geographic Reach
1 country

3 active sites

Status
unknown

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

First Submitted

Initial submission to the registry

December 22, 2005

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 23, 2005

Completed
9 days until next milestone

Study Start

First participant enrolled

January 1, 2006

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2007

Completed
Last Updated

January 11, 2007

Status Verified

September 1, 2006

First QC Date

December 22, 2005

Last Update Submit

January 10, 2007

Conditions

Tobacco Use DisorderAlcohol AbuseLack of Physical ActivityPoor Diet

Keywords

Tobacco use

Outcome Measures

Primary Outcomes (1)

  • The primary outcome of interest is the referral rate for any unhealthy behavior to the CHERL with the predictor variable being referral-only versus consultant-enhanced practices.

Secondary Outcomes (1)

  • Aim 2 of the study is to determine if the patients referred to the CHERL demonstrate health behavior improvements.

Interventions

CHERLBEHAVIORAL

Eligibility Criteria

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

You may qualify if:

  • Patients, clinicians, and their staff participating in this GRIN study.

You may not qualify if:

  • Patients, clinicians, and their staff who are not participating in this GRIN study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (3)

Genesys Health System

Flint, Michigan, 48446, United States

RECRUITING

MCRC

Grand Rapids, Michigan, 48823, United States

RECRUITING

UP Health Education Corporation

Marquette, Michigan, 49855, United States

RECRUITING

MeSH Terms

Conditions

Tobacco Use DisorderAlcoholismSedentary BehaviorTobacco Use

Condition Hierarchy (Ancestors)

Substance-Related DisordersChemically-Induced DisordersMental DisordersAlcohol-Related DisordersBehavior

Study Officials

  • Jodi Holtrop, PhD

    Michigan State University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Annette M Sokolnicki

CONTACT

517/353-0772annette.sokolnicki@hc.msu.edu

Jodi Holtrop

CONTACT

517/353-0772

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
DOUBLE
Purpose
ECT
Intervention Model
CROSSOVER
Sponsor Type
NETWORK

Study Record Dates

First Submitted

December 22, 2005

First Posted

December 23, 2005

Study Start

January 1, 2006

Study Completion

February 1, 2007

Last Updated

January 11, 2007

Record last verified: 2006-09

Locations

US(3)