DM-TBSI: Telephone Delivered Behavioral Skills Intervention for Blacks With T2DM

Sponsor
Medical College of Wisconsin (Other)
Overall Status
Completed
CT.gov ID
NCT00929838
Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
256
1
4
94
2.7

Study Details

Study Description

Brief Summary

Blacks or African Americans have greater risk of and are more likely to die from type 2 diabetes (T2DM). Major barriers to effective diabetes care for Blacks include poor diabetes knowledge, self-management skills, empowerment, and perceived control. Few prior studies have tested interventions to address these barriers in combination, especially among Blacks who have the greatest burden of diabetes related complications. This study provides a unique opportunity to address this gap in the literature by testing the efficacy of separate and combined telephone-delivered, diabetes knowledge and motivation/behavioral skills training intervention in high risk Blacks with poorly controlled T2DM. The findings of this study, if successful, will provide new information on how to improve quality of care for diabetes in ethnic minorities and reduce the disproportionate burden of diabetes complications and deaths in this population.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Diabetes Knowledge/Information
  • Behavioral: Motivation/Behavioral Skills
  • Behavioral: Combined Intervention
  • Behavioral: Usual Care
N/A

Detailed Description

Blacks (African Americans) with Type 2 diabetes (T2DM) have higher prevalence of diabetes, poorer metabolic control, and greater risk for complications and death compared to Whites. Poor outcomes in Blacks with T2DM can be attributed to patient, provider, and health systems level factors. Provider and health system factors account for <10% of variance in major diabetes outcomes. Key differences appear to be at the patient level. Of the patient level factors, consistent differences between Blacks and Whites with T2DM have been found in diabetes knowledge, self-management skills, empowerment, and perceived control. A variety of interventions to improve diabetes self-management have been tested including: 1) knowledge interventions; 2) lifestyle interventions; 3) skills training interventions; and 4) patient activation and empowerment interventions. Most of these interventions have been tested individually, but rarely have they been tested in combination, especially among Blacks who have the greatest burden of diabetes related complications. This study provides a unique opportunity to address this gap in the literature. Using a 2x2 factorial design, this study will test the efficacy of separate and combined telephone-delivered, diabetes knowledge/information and motivation/behavioral skills training intervention in high risk Blacks with poorly controlled T2DM (HbA1c ≥9%). The primary objective is to test the separate and combined efficacy of a telephone-delivered diabetes knowledge/information intervention and motivation/behavioral skills training intervention in improving HbA1c levels in Blacks with T2DM using a 2x2 factorial design. The secondary objectives are: 1) To determine whether patients randomized to the telephone-delivered diabetes knowledge/information intervention, the motivation/behavioral skills training intervention or the combined intervention will have greater improvement in physical activity, diet, medication adherence, and self-monitoring of blood glucose at 12 months of follow-up compared to usual care; and 2) To determine the cost-effectiveness of each telephone intervention separately, and then in combination. The primary outcome is HbA1c level at 12 months of follow-up. The secondary outcomes are cost-effectiveness of each telephone intervention separately, and then in combination, and change in physical activity, diet, medication adherence, and self-monitoring of blood glucose over 12 months of follow-up. The long-term goal of the project is to achieve improvement in diabetes-related outcomes in this patient population.

Study Design

Study Type:
Interventional
Actual Enrollment :
256 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Telephone Delivered Behavioral Skills Intervention for Blacks With T2DM
Study Start Date :
Aug 1, 2008
Actual Primary Completion Date :
Jun 1, 2016
Actual Study Completion Date :
Jun 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Diabetes Knowledge/Information Arm

Subjects randomized to the diabetes knowledge/information arm will complete 12 diabetes education modules over a 12-week period. The educational materials were developed based on guidelines for diabetes education by the American Diabetes Association. The content is based on the principles of the Adult Learning Theory. The information is designed to be relevant, person centered, and presented in a non-threatening manner. The modules are designed to be delivered via telephone in 10-15 minutes, so that the maximum contact time per telephone call including introduction and closing would not exceed 30 minutes.

Behavioral: Diabetes Knowledge/Information
This group will receive telephone-delivered diabetes knowledge/information lasting 30 minutes for 12 weeks.

Experimental: Motivation/Behavioral Skills Arm

The motivation/behavioral skills intervention consists of patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The behavioral skills training will be focused on 4 behaviors - physical activity, diet, medication adherence, and glucose self-monitoring. Guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks (4 behaviors over 12 weeks).

Behavioral: Motivation/Behavioral Skills
This intervention consists of patient activation, patient empowerment, and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks.

Experimental: Combined Intervention Arm

The combined intervention group will receive weekly telephone-delivered diabetes knowledge/information, patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone. The behavioral skills training will be focused on 4 behaviors and guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks. The combined intervention group telephone sessions will last for 30 minutes.

Behavioral: Combined Intervention
This group will receive all components of the diabetes knowledge/information and the motivation/behavioral skills interventions via telephone lasting 30 minutes every week for 12 weeks.

Sham Comparator: Usual Care Arm

The usual care group will receive weekly telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention. Patients in the usual care group will continue to receive any usual diabetes education provided by the clinic staff; however, they will not receive targeted diabetes knowledge/information, activation, empowerment, or behavioral skills training.

Behavioral: Usual Care
This group will receive telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention and content.

Outcome Measures

Primary Outcome Measures

  1. Hemoglobin A1c (HbA1c) at 12 Months Post Randomization [12-months post randomization]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
    1. Age ≥18 years
    1. Clinical diagnosis of T2DM and HbA1c ≥9% at the screening visit
    1. Self-identified as Black or African American
    1. Subject must be taking at least one oral medication for diabetes, hypertension, or hyperlipidemia and must be willing to use the MEMS cap and bottle for 12 months
    1. Subjects must be able to communicate in English
    1. Subjects must have access to a telephone (landline or cell phone) for the 12 week intervention period
Exclusion Criteria:
    1. Mental confusion on interview suggesting significant dementia
    1. Participation in other diabetes clinical trials
    1. Alcohol or drug abuse/dependency
    1. Active psychosis or acute mental disorder
    1. Life expectancy <6 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of South Carolina Charleston South Carolina United States 29425

Sponsors and Collaborators

  • Medical College of Wisconsin
  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Investigators

  • Principal Investigator: Leonard E Egede, MD, MS, Medical University of South Carolina (MUSC)

Study Documents (Full-Text)

More Information

Additional Information:

Publications

Responsible Party:
Egede, Leonard E, Professor of Medicine, Chief Division of General Internal Medicine, Medical College of Wisconsin
ClinicalTrials.gov Identifier:
NCT00929838
Other Study ID Numbers:
  • DK81121
  • R01DK081121
  • R01DK081121-01A1
  • HR18334
First Posted:
Jun 30, 2009
Last Update Posted:
Jul 8, 2021
Last Verified:
Jun 1, 2021
Keywords provided by Egede, Leonard E, Professor of Medicine, Chief Division of General Internal Medicine, Medical College of Wisconsin
Additional relevant MeSH terms:

Study Results

Participant Flow

Recruitment Details
Pre-assignment Detail
Arm/Group Title Diabetes Knowledge/Information Arm Motivation/Behavioral Skills Arm Combined Intervention Arm Usual Care Arm
Arm/Group Description Subjects randomized to the diabetes knowledge/information arm will complete 12 diabetes education modules over a 12-week period. The educational materials were developed based on guidelines for diabetes education by the American Diabetes Association. The content is based on the principles of the Adult Learning Theory. The information is designed to be relevant, person centered, and presented in a non-threatening manner. The modules are designed to be delivered via telephone in 10-15 minutes, so that the maximum contact time per telephone call including introduction and closing would not exceed 30 minutes. Diabetes Knowledge/Information: This group will receive telephone-delivered diabetes knowledge/information lasting 30 minutes for 12 weeks. The motivation/behavioral skills intervention consists of patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The behavioral skills training will be focused on 4 behaviors - physical activity, diet, medication adherence, and glucose self-monitoring. Guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks (4 behaviors over 12 weeks). Motivation/Behavioral Skills: This intervention consists of patient activation, patient empowerment, and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The combined intervention group will receive weekly telephone-delivered diabetes knowledge/information, patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone. The behavioral skills training will be focused on 4 behaviors and guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks. The combined intervention group telephone sessions will last for 30 minutes. Combined Intervention: This group will receive all components of the diabetes knowledge/information and the motivation/behavioral skills interventions via telephone lasting 30 minutes every week for 12 weeks. The usual care group will receive weekly telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention. Patients in the usual care group will continue to receive any usual diabetes education provided by the clinic staff; however, they will not receive targeted diabetes knowledge/information, activation, empowerment, or behavioral skills training. Usual Care: This group will receive telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention and content.
Period Title: Overall Study
STARTED 63 65 63 64
COMPLETED 53 56 53 55
NOT COMPLETED 10 9 10 9

Baseline Characteristics

Arm/Group Title Diabetes Knowledge/Information Arm Motivation/Behavioral Skills Arm Combined Intervention Arm Usual Care Arm Total
Arm/Group Description Subjects randomized to the diabetes knowledge/information arm will complete 12 diabetes education modules over a 12-week period. The educational materials were developed based on guidelines for diabetes education by the American Diabetes Association. The content is based on the principles of the Adult Learning Theory. The information is designed to be relevant, person centered, and presented in a non-threatening manner. The modules are designed to be delivered via telephone in 10-15 minutes, so that the maximum contact time per telephone call including introduction and closing would not exceed 30 minutes. Diabetes Knowledge/Information: This group will receive telephone-delivered diabetes knowledge/information lasting 30 minutes for 12 weeks. The motivation/behavioral skills intervention consists of patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The behavioral skills training will be focused on 4 behaviors - physical activity, diet, medication adherence, and glucose self-monitoring. Guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks (4 behaviors over 12 weeks). Motivation/Behavioral Skills: This intervention consists of patient activation, patient empowerment, and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The combined intervention group will receive weekly telephone-delivered diabetes knowledge/information, patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone. The behavioral skills training will be focused on 4 behaviors and guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks. The combined intervention group telephone sessions will last for 30 minutes. Combined Intervention: This group will receive all components of the diabetes knowledge/information and the motivation/behavioral skills interventions via telephone lasting 30 minutes every week for 12 weeks. The usual care group will receive weekly telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention. Patients in the usual care group will continue to receive any usual diabetes education provided by the clinic staff; however, they will not receive targeted diabetes knowledge/information, activation, empowerment, or behavioral skills training. Usual Care: This group will receive telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention and content. Total of all reporting groups
Overall Participants 63 65 63 64 255
Age (Count of Participants)
<=18 years
0
0%
0
0%
0
0%
0
0%
0
0%
Between 18 and 65 years
48
76.2%
51
78.5%
48
76.2%
52
81.3%
199
78%
>=65 years
15
23.8%
14
21.5%
15
23.8%
12
18.8%
56
22%
Sex: Female, Male (Count of Participants)
Female
28
44.4%
25
38.5%
30
47.6%
31
48.4%
114
44.7%
Male
35
55.6%
40
61.5%
33
52.4%
33
51.6%
141
55.3%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native
0
0%
0
0%
0
0%
0
0%
0
0%
Asian
0
0%
0
0%
0
0%
0
0%
0
0%
Native Hawaiian or Other Pacific Islander
0
0%
0
0%
0
0%
0
0%
0
0%
Black or African American
63
100%
65
100%
63
100%
64
100%
255
100%
White
0
0%
0
0%
0
0%
0
0%
0
0%
More than one race
0
0%
0
0%
0
0%
0
0%
0
0%
Unknown or Not Reported
0
0%
0
0%
0
0%
0
0%
0
0%

Outcome Measures

1. Primary Outcome
Title Hemoglobin A1c (HbA1c) at 12 Months Post Randomization
Description
Time Frame 12-months post randomization

Outcome Measure Data

Analysis Population Description
Final analysis used baseline A1c analysis of covariance for differences in levels of A1c between the treatment groups at 12months with baseline A1c as covariate.
Arm/Group Title Diabetes Knowledge/Information Arm Motivation/Behavioral Skills Arm Combined Intervention Arm Usual Care Arm
Arm/Group Description Subjects randomized to the diabetes knowledge/information arm will complete 12 diabetes education modules over a 12-week period. The educational materials were developed based on guidelines for diabetes education by the American Diabetes Association. The content is based on the principles of the Adult Learning Theory. The information is designed to be relevant, person centered, and presented in a non-threatening manner. The modules are designed to be delivered via telephone in 10-15 minutes, so that the maximum contact time per telephone call including introduction and closing would not exceed 30 minutes. Diabetes Knowledge/Information: This group will receive telephone-delivered diabetes knowledge/information lasting 30 minutes for 12 weeks. The motivation/behavioral skills intervention consists of patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The behavioral skills training will be focused on 4 behaviors - physical activity, diet, medication adherence, and glucose self-monitoring. Guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks (4 behaviors over 12 weeks). Motivation/Behavioral Skills: This intervention consists of patient activation, patient empowerment, and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The combined intervention group will receive weekly telephone-delivered diabetes knowledge/information, patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone. The behavioral skills training will be focused on 4 behaviors and guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks. The combined intervention group telephone sessions will last for 30 minutes. Combined Intervention: This group will receive all components of the diabetes knowledge/information and the motivation/behavioral skills interventions via telephone lasting 30 minutes every week for 12 weeks. The usual care group will receive weekly telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention. Patients in the usual care group will continue to receive any usual diabetes education provided by the clinic staff; however, they will not receive targeted diabetes knowledge/information, activation, empowerment, or behavioral skills training. Usual Care: This group will receive telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention and content.
Measure Participants 63 65 63 64
Mean (Standard Deviation) [percentage of glycosylated hemoglobin]
9.3
(1.8)
9.2
(2.1)
9.2
(1.9)
9.5
(2.5)

Adverse Events

Time Frame 12 months
Adverse Event Reporting Description
Arm/Group Title Diabetes Knowledge/Information Arm Motivation/Behavioral Skills Arm Combined Intervention Arm Usual Care Arm
Arm/Group Description Subjects randomized to the diabetes knowledge/information arm will complete 12 diabetes education modules over a 12-week period. The educational materials were developed based on guidelines for diabetes education by the American Diabetes Association. The content is based on the principles of the Adult Learning Theory. The information is designed to be relevant, person centered, and presented in a non-threatening manner. The modules are designed to be delivered via telephone in 10-15 minutes, so that the maximum contact time per telephone call including introduction and closing would not exceed 30 minutes. Diabetes Knowledge/Information: This group will receive telephone-delivered diabetes knowledge/information lasting 30 minutes for 12 weeks. The motivation/behavioral skills intervention consists of patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The behavioral skills training will be focused on 4 behaviors - physical activity, diet, medication adherence, and glucose self-monitoring. Guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks (4 behaviors over 12 weeks). Motivation/Behavioral Skills: This intervention consists of patient activation, patient empowerment, and behavioral skills training delivered via telephone lasting 30 minutes every week for 12 weeks. The combined intervention group will receive weekly telephone-delivered diabetes knowledge/information, patient activation (list of 5 questions to ask their provider at every visit and training on how to ask the questions), patient empowerment (diabetes responsibility contracts, personal goals, and flow charts for patients to record lab results/medications and training on how to use the empowerment tools), and behavioral skills training delivered via telephone. The behavioral skills training will be focused on 4 behaviors and guided by subjects' current problem areas and preferences, subjects will be asked to choose 1 of 4 behaviors to focus on every 3 weeks. The combined intervention group telephone sessions will last for 30 minutes. Combined Intervention: This group will receive all components of the diabetes knowledge/information and the motivation/behavioral skills interventions via telephone lasting 30 minutes every week for 12 weeks. The usual care group will receive weekly telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention. Patients in the usual care group will continue to receive any usual diabetes education provided by the clinic staff; however, they will not receive targeted diabetes knowledge/information, activation, empowerment, or behavioral skills training. Usual Care: This group will receive telephone-delivered general health education lasting 30 minutes for 12 weeks to control for attention and content.
All Cause Mortality
Diabetes Knowledge/Information Arm Motivation/Behavioral Skills Arm Combined Intervention Arm Usual Care Arm
Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/63 (0%) 0/65 (0%) 0/63 (0%) 0/64 (0%)
Serious Adverse Events
Diabetes Knowledge/Information Arm Motivation/Behavioral Skills Arm Combined Intervention Arm Usual Care Arm
Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/63 (0%) 0/65 (0%) 0/63 (0%) 0/64 (0%)
Other (Not Including Serious) Adverse Events
Diabetes Knowledge/Information Arm Motivation/Behavioral Skills Arm Combined Intervention Arm Usual Care Arm
Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/63 (0%) 0/65 (0%) 0/63 (0%) 0/64 (0%)

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Jennifer Campbell
Organization Medical College of Wisconsin
Phone 414-955-8829
Email jacampbell@mcw.edu
Responsible Party:
Egede, Leonard E, Professor of Medicine, Chief Division of General Internal Medicine, Medical College of Wisconsin
ClinicalTrials.gov Identifier:
NCT00929838
Other Study ID Numbers:
  • DK81121
  • R01DK081121
  • R01DK081121-01A1
  • HR18334
First Posted:
Jun 30, 2009
Last Update Posted:
Jul 8, 2021
Last Verified:
Jun 1, 2021