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Motivational Interviewing and Cognitive Behavioral Therapy-based Intervention for Cardiovascular Disease Prevention Amongst American Indians With Diabetic and Depressive Symptoms

Primary Purpose

Cardiovascular Diseases, Diabetes Mellitus, Type 2, Depression

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Motivational Interviewing/Cognitive Behavioral-based Therapy
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cardiovascular Diseases focused on measuring Motivational Interviewing, Cognitive Therapy, Community-Based Participatory Research, Indians, North American

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Be 18 years of age or older
  • Be an American Indian/Alaska Native
  • Currently reside on or within 20 miles of the Tribal reservation boundary
  • Have a Body Mass Index > 25
  • Have a PSS (10 item) score > 15
  • Be pre-diabetic for Type 2 diabetes (via self-report, health provider referral, or previous glucose reading or hemoglobin A1c reading indicating pre-diabetes within the past 12 months) or have been diagnosed as having Type 2 diabetes
  • If a woman, not currently pregnant

Exclusion Criteria:

  • Referred to their physician for approval of participation during the baseline assessment process and the physician does not give approval or the participant refused to follow-up on the referral
  • Unstable or exhibits serious psychiatric symptoms as determined by project's tribal mental health specialist

Sites / Locations

  • University of Washington, Indigenous Wellness Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Motivational Interviewing/Cognitive Behavioral-based Therapy

Wait-List Control

Arm Description

Receives an immediate weekly 10 session intervention based on a culturally-adapted, motivational interviewing and Cognitive Behavioral Therapy grounded protocol.

Receives a weekly 10 session intervention based on a culturally-adapted, motivational interviewing and Cognitive Behavioral Therapy grounded protocol after a three month, no-intervention waiting period.

Outcomes

Primary Outcome Measures

Change in Body Mass Index
The investigators will compare changes in body mass index between the wait-list control group and the immediate intervention group, and also for each individual over time.

Secondary Outcome Measures

Changes in Depressive Symptoms using the Center for Epidemiologic Studies Depression Scale (CES-D)
The investigators will compare changes in depressive symptoms as measured by the CES-D 10-item scale between the wait-list control group and the immediate intervention group, and also for each individual over time.
Changes in Blood Lipids
The investigators will compare changes in mg/dL of blood lipids (Total cholesterol, HDL-C, LDL-C, triglycerides) between the wait-list control group and the immediate intervention group, and also for each individual over time.
Changes in Blood Glucose
The investigators will compare changes in mg/dL blood glucose between the wait-list control group and the immediate intervention group, and also for each individual over time.
Changes in Hemoglobin A1c
The investigators will compare changes in percent hemoglobin A1c between the wait-list control group and the immediate intervention group, and also for each individual over time.
Changes in Blood Pressure
The investigators will compare changes in mmHg blood pressure levels between the wait-list control group and the immediate intervention group, and also for each individual over time.

Full Information

First Posted
June 28, 2013
Last Updated
December 11, 2015
Sponsor
University of Washington
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)
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1. Study Identification

Unique Protocol Identification Number
NCT01892124
Brief Title
Motivational Interviewing and Cognitive Behavioral Therapy-based Intervention for Cardiovascular Disease Prevention Amongst American Indians With Diabetic and Depressive Symptoms
Official Title
Healthy Hearts, Healthy Minds
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
November 2013 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Institute on Minority Health and Health Disparities (NIMHD)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
American Indians (AIs) living in the Northwest have very high rates of diabetes, obesity, tobacco use, depression, and other risk factors associated with cardiovascular disease. Depression and diabetes have a pernicious effect on CVD risk and susceptibility. This study seeks to build upon the success of the 1-month, 5-session motivational interviewing (MI) CVD prevention component of the həli?dxw Project (aka Healthy Hearts-originally funded under RFA-HL-06-002; U01 HL HL087322-05). həli?dxw successfully culturally adapted MI for CVD prevention for AIs, trained AIs to implement the intervention, and conducted a preliminary feasibility and efficacy trial. Initial results indicated that participants enthusiastically embraced the MI component of the program; however, observations of the counselors, survey data, and feedback from participants suggest that depressive symptomatology served as a barrier to achieving CVD preventive behaviors and desired outcomes; and, that more time and attention to underlying depressive symptomatology may enhance motivation and CVD prevention behaviors, particularly among AIs with pre-diabetes and Type 2 diabetes. Building upon solid preliminary CVD epidemiological data, preliminary acceptability and feasibility of utilizing an MI approach, and motivated by the need to address elevated depression and diabetes profiles from the həli?dxw study, the investigators will develop a 3-month, 10-session MI-based cognitive-behavioral-adherence (MI-CBT-CVD) treatment program to address underlying depressive symptomatology, activate CVD prevention behaviors, and decrease BMI and CVD risk behaviors among 50 pre-and recently diagnosed diabetic AIs at risk for CVD. The study proposes three innovative and significant aims. First, in line with community-based participatory (CBPR) principles and pre-established indigenous research protocols with the tribal community, the investigators will conduct formative research to develop the MI-CBT-CVD intervention. Second, the investigators will conduct a pilot randomized two-group, single-site waitlist-controlled clinical trial of a 10-session, 3-month MI-based cognitive-behavioral treatment for CVD prevention (MI-CBT-CVD) among 50 pre-and recently diagnosed diabetic AI adults with depressive symptomatology and who are also at risk for CVD. Assessments will be conducted at pre and post intervention and at 6-months (3 month follow-up). Third, the investigators will disseminate the findings to the tribe as well as research outlets and prepare an RO1 to conduct a full-scale RCT should the pilot intervention be efficacious, acceptable to the community, and feasible. The primary objectives will be to determine the effect of the proposed culturally-grounded behavioral intervention program on (a) reducing weight as measured by BMI (7-10% reduction in BMI); (b) decreasing depressive symptomatology; (c) increasing physical activity; (d) decreasing sedentary activities; (d) increasing healthful food habits; and (e) improving biomedical outcomes (e.g., blood lipid profiles, glucose, hemoglobin A1C, and blood pressure). The intervention will be culturally relevant and utilize existing Native resources and personnel wherever possible.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Diabetes Mellitus, Type 2, Depression, Dysthymic Disorder
Keywords
Motivational Interviewing, Cognitive Therapy, Community-Based Participatory Research, Indians, North American

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Motivational Interviewing/Cognitive Behavioral-based Therapy
Arm Type
Experimental
Arm Description
Receives an immediate weekly 10 session intervention based on a culturally-adapted, motivational interviewing and Cognitive Behavioral Therapy grounded protocol.
Arm Title
Wait-List Control
Arm Type
Experimental
Arm Description
Receives a weekly 10 session intervention based on a culturally-adapted, motivational interviewing and Cognitive Behavioral Therapy grounded protocol after a three month, no-intervention waiting period.
Intervention Type
Behavioral
Intervention Name(s)
Motivational Interviewing/Cognitive Behavioral-based Therapy
Primary Outcome Measure Information:
Title
Change in Body Mass Index
Description
The investigators will compare changes in body mass index between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Secondary Outcome Measure Information:
Title
Changes in Depressive Symptoms using the Center for Epidemiologic Studies Depression Scale (CES-D)
Description
The investigators will compare changes in depressive symptoms as measured by the CES-D 10-item scale between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Title
Changes in Blood Lipids
Description
The investigators will compare changes in mg/dL of blood lipids (Total cholesterol, HDL-C, LDL-C, triglycerides) between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Title
Changes in Blood Glucose
Description
The investigators will compare changes in mg/dL blood glucose between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Title
Changes in Hemoglobin A1c
Description
The investigators will compare changes in percent hemoglobin A1c between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Title
Changes in Blood Pressure
Description
The investigators will compare changes in mmHg blood pressure levels between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Other Pre-specified Outcome Measures:
Title
Changes in Physical Activity
Description
The investigators will compare changes in physical activity levels between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Title
Changes in Sedentary Activity
Description
The investigators will compare changes in sedentary activity levels between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints
Title
Changes in Food Habits
Description
The investigators will compare changes in food habits between the wait-list control group and the immediate intervention group, and also for each individual over time.
Time Frame
Assessed at baseline, 3 month, and 6 month timepoints

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Be 18 years of age or older Be an American Indian/Alaska Native Currently reside on or within 20 miles of the Tribal reservation boundary Have a Body Mass Index > 25 Have a PSS (10 item) score > 15 Be pre-diabetic for Type 2 diabetes (via self-report, health provider referral, or previous glucose reading or hemoglobin A1c reading indicating pre-diabetes within the past 12 months) or have been diagnosed as having Type 2 diabetes If a woman, not currently pregnant Exclusion Criteria: Referred to their physician for approval of participation during the baseline assessment process and the physician does not give approval or the participant refused to follow-up on the referral Unstable or exhibits serious psychiatric symptoms as determined by project's tribal mental health specialist
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karina L Walters, MSW, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rachelle McCarty, ND, MPH
Organizational Affiliation
University of Washington
Official's Role
Study Director
Facility Information:
Facility Name
University of Washington, Indigenous Wellness Research Institute
City
Seattle
State/Province
Washington
ZIP/Postal Code
98105
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22965622
Citation
Walters KL, LaMarr J, Levy RL, Pearson C, Maresca T, Mohammed SA, Simoni JM, Evans-Campbell T, Fredriksen-Goldsen K, Fryberg S, Jobe JB; həli?dxw Intervention Team. Project həli?dx(w)/Healthy Hearts Across Generations: development and evaluation design of a tribally based cardiovascular disease prevention intervention for American Indian families. J Prim Prev. 2012 Aug;33(4):197-207. doi: 10.1007/s10935-012-0274-z.
Results Reference
background
PubMed Identifier
22530859
Citation
Mohammed SA, Walters KL, Lamarr J, Evans-Campbell T, Fryberg S. Finding middle ground: negotiating university and tribal community interests in community-based participatory research. Nurs Inq. 2012 Jun;19(2):116-27. doi: 10.1111/j.1440-1800.2011.00557.x. Epub 2011 Jul 15.
Results Reference
background
Links:
URL
http://www.iwri.org/
Description
Indigenous Wellness Research Institute at the University of Washington

Learn more about this trial

Motivational Interviewing and Cognitive Behavioral Therapy-based Intervention for Cardiovascular Disease Prevention Amongst American Indians With Diabetic and Depressive Symptoms

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