Improving Health Behaviors Through Telephone Linked Care
Study That Examines Integration of the Telephone Linked Care Behavioral Change (Automated Counseling) System Into Primary Care
1 other identifier
interventional
400
1 country
1
Brief Summary
The investigators propose to conduct a randomized controlled trial at the patient level of the Telephone Linked Care - Behavioral Change (TLC-BC) system, which is designed to promote smoking cessation, reduce risky drinking, and improve physical activity and diet. They expect to:
- 1.successfully integrate an automated telephone behavior change intervention into primary care practices;
- 2.demonstrate improvement in health behaviors for individuals randomized (assigned by systematic chance) to use the TLC-BC system compared to individuals who receive written health education informational packets; and
- 3.evaluate the direct costs associated with the use and operation of the TLC-BC system.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2006
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2006
CompletedFirst Submitted
Initial submission to the registry
April 11, 2006
CompletedFirst Posted
Study publicly available on registry
April 13, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2007
CompletedSeptember 26, 2007
September 1, 2007
April 11, 2006
September 24, 2007
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
At 6 months a clinically significant improvement in behavioral change rates will be demonstrated for diet, physical activity and smoking in the intervention group compared to patients in the control group
6 months
At baseline, 3, 6, and 9 months risky drinking will be identified, but there will be no difference in improvement between the study groups.
baseline, 3, 6, and 9 months
Interventions
Eligibility Criteria
You may qualify if:
- years or older
- Capable of giving informed consent
- Reliable access to a phone
- Able to read English
You may not qualify if:
- Less than 18 years of age
- Not capable of giving informed consent
- No reliable access to a phone
- Unable to read English (including blindness)
- Too ill to participate
- Not willing to allow the Telephone Linked Care - Behavior Change system to provide health information reports based on responses to physician
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
American Academy of Family Physicians National Research Network
Leawood, Kansas, 66211-2672, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Wilson D Pace, MD, FAAFP
American Academy of Family Physicians National Research Network
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
April 11, 2006
First Posted
April 13, 2006
Study Start
April 1, 2006
Study Completion
June 1, 2007
Last Updated
September 26, 2007
Record last verified: 2007-09