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| Name | Class |
|---|---|
| Robert Wood Johnson Foundation | OTHER |
| Agency for Healthcare Research and Quality (AHRQ) | FED |
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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:
Project aims and hypotheses follow:
Aim 1: Integrate a proven, totally automated computer telephone intervention, Telephone Linked Care - Behavior Change (TLC-BC), into primary care practices. This will be assessed by the patient and clinician/staff surveys at the end of data collection.
Aim 2: Demonstrate an improvement in health behaviors for individuals randomized to use the TLC-BC system compared to individuals who receive written informational packets.
Aim 3: Evaluate the direct costs associated with the use and operation of the TLC-BC system within the primary care setting.
Hypothesis 1: The Telephone Linked Care - Behavioral Change system will be successfully implemented by patients and practices.
Hypothesis 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.
Hypothesis 3: At baseline, 3, 6, and 9 months risky drinking will be identified, but there will be no difference in improvement between the study groups.
See above
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Telephone Linked Care - Behavior Change Counseling System | Behavioral | |||
| Telephone-linked behavioral counseling | Behavioral |
| Measure | Description | Time Frame |
|---|---|---|
| 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Wilson D Pace, MD, FAAFP | American Academy of Family Physicians National Research Network | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| American Academy of Family Physicians National Research Network | Leawood | Kansas | 66211-2672 | United States |
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| ID | Term |
|---|---|
| D009043 | Motor Activity |
| D012907 | Smoking |
| D000437 | Alcoholism |
| ID | Term |
|---|---|
| D001519 | Behavior |
| D019973 | Alcohol-Related Disorders |
| D019966 | Substance-Related Disorders |
| D064419 | Chemically-Induced Disorders |
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| D001523 | Mental Disorders |