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Self-Management Addressing Heart Disease Risk Trial (SMAHRT)

Primary Purpose

Bipolar Disorder, Cardiovascular Disease

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Chronic care model for Bipolar Disorder
Sponsored by
US Department of Veterans Affairs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Bipolar Disorder focused on measuring Chronic Illness, Disease management, Health Behaviors, Mood Disorders-Bipolar

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosis of bipolar disorder (I, II, not otherwise specified, or schizoaffective-bipolar subtype)
  • Have a diagnosis or be at risk for arteriosclerotic cardiovascular disease (ASCVD).

We define this as a patient having a current diagnosis of or receiving treatment for at least one of the following medical conditions:

  • hyperlipidemia or dyslipidemia (documented diagnosis or low-density lipoprotein >=160, or receiving statin or other treatment)
  • hypertension (documented diagnosis or blood pressure of >=140/90 on 2 occasions)
  • diabetes mellitus (documented diagnosis or HbA1C >=7%, or receiving treatment)
  • obesity (documented diagnosis or BMI >30), based on medical record review of current problems
  • current ASCVD diagnosis

Exclusion Criteria:

  • Have unresolved substance intoxication or withdrawal, such as appearing to be intoxicated (e.g., incoherent, slurred speech), or experiencing withdrawal symptoms from substance abuse at the time of enrollment.
  • Are already enrolled in a mental health program with a mobile outreach component in which clinical caregivers deliver services to the patient in the community (e.g., assertive community treatment or intensive case management). These patients may be receiving similar services to those offered in the intervention.
  • Are unwilling or unable to provide informed consent or comply with study requirements at the time of enrollment (e.g., unable to complete forms or attend scheduled sessions due to serious illness or substantial functional limitations).

Sites / Locations

  • VA Ann Arbor Healthcare System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Chronic Care Model for Bipolar Disorder

Enhanced Usual Care

Arm Description

An intervention group of patients with bipolar disorder and 1 or more risk factor for cardiovascular disease; group will receive self-management group sessions, followed by phone contacts by the Care Manager. This is the chronic care model for bipolar disorder

A group of patients with bipolar disorder and one or more risk factors for cardiovascular disease will be randomized to receive enhanced usual care. This group will receive usual care, plus mailings on wellness topics (attention control), and their providers will receive information on guideline concordant care.

Outcomes

Primary Outcome Measures

Systolic and Diastolic Blood Pressure (SBP, DBP)
24-month systolic and diastolic blood pressure (mm/Hg): lower is better
Total Cholesterol
Total cholesterol in mg/dl- lower is better
Physical Health-related Quality of Life Score
Physical health-related quality of life is based on the Short Form (SF)-12 survey physical health component (PCS) score- which ranges from 0 to 50, with higher scores indicating higher quality of life

Secondary Outcome Measures

Manic Symptoms
Manic symptoms based on the Internal State Scale (range is 0-500; higher score indicates more severe symptoms)
Depressive Symptom Score
Depressive symptoms based on the Internal State Scale (Range: 0-200, higher score = more severe symptoms)
Disability Based on WHO-DAS Score
Disability based on the WHO Disability Assessment Scale (WHO-DAS); range = 0-24, higher score equals greater disability
Body Mass Index (BMI)
Body mass index (BMI) is reported in kilograms divided by meters squared (kg/m^2) with a normal (healthy) range of 18-24, in which >=25 is considered overweight, and >=30 is the definition of obesity

Full Information

First Posted
July 9, 2007
Last Updated
November 12, 2014
Sponsor
US Department of Veterans Affairs
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1. Study Identification

Unique Protocol Identification Number
NCT00499096
Brief Title
Self-Management Addressing Heart Disease Risk Trial
Acronym
SMAHRT
Official Title
Cardiovascular Risk Factors in Veterans With Bipolar Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
May 2012 (Actual)
Study Completion Date
November 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research study is to learn whether or not people with bipolar disorder can reduce their risk of heart disease and related conditions by having a Care Manager provide self management and care management.
Detailed Description
Background: Bipolar disorder is associated with significant personal and societal costs, and represents a substantial burden to the VA. Medical conditions, notably cardiovascular disease (CVD), are substantial contributors to increased morbidity and mortality in patients with bipolar disorder, in part because of behavioral and treatment factors. Despite the existence of effective medications for managing CVD-related risk factors (e.g., hypertension, hyperlipidemia, diabetes, obesity), outcomes for these conditions remain suboptimal among patients with bipolar disorder. Objectives: The immediate objective of this study is to determine whether a manual-based Chronic Care Model (CCM) intervention compared to usual VA care improves control of intermediate physiological measures that represent risk factors of CVD for veterans with bipolar disorder. We hypothesize that, within 12 months of the intervention initiation, patients receiving the CCM intervention will be more likely to demonstrate improved control of CVD-related risk factors (blood pressure, fasting cholesterol) and report improved physical health-related quality of life. Methods: This is a prospective, randomized, controlled, single-blind, single-site behavioral intervention trial of adult patients with a diagnosis of bipolar disorder receiving care in the VA Ann Arbor Healthcare System. Up to 300 subjects will be enrolled, of which 150 will be randomized to receive the intervention and 150 will receive usual VA care. All subjects will complete a baseline clinical assessment and then subsequent follow-up assessments at 3, 6, 12, and 24 months. The intervention's three core components will be implemented by a nurse Care Manager and include: 1) self-management behavioral sessions for patients addressing the reduction of CVD risk factors through symptom control and behavior change based on Social Cognitive Theory, 2) care management to promote patient behavior change and coordinate care, and 3) implementation of practice guidelines for providers on management of CVD risk factors in patients with bipolar disorder. Medical and psychiatric care, including medications, will continue to be provided by the patient's usual providers. Usual VA care will be enhanced and consist of guideline implementation and general patient education (attention control), but will not include self-management sessions or Care Manager contacts. Primary clinical outcomes include changes in cholesterol, and health-related quality of life (SF-12 physical health summary score). Linear regression models will be used to determine the effect of the intervention on each outcome. Mediators of treatment effect including symptoms and health behaviors will also be assessed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder, Cardiovascular Disease
Keywords
Chronic Illness, Disease management, Health Behaviors, Mood Disorders-Bipolar

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
118 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Chronic Care Model for Bipolar Disorder
Arm Type
Experimental
Arm Description
An intervention group of patients with bipolar disorder and 1 or more risk factor for cardiovascular disease; group will receive self-management group sessions, followed by phone contacts by the Care Manager. This is the chronic care model for bipolar disorder
Arm Title
Enhanced Usual Care
Arm Type
No Intervention
Arm Description
A group of patients with bipolar disorder and one or more risk factors for cardiovascular disease will be randomized to receive enhanced usual care. This group will receive usual care, plus mailings on wellness topics (attention control), and their providers will receive information on guideline concordant care.
Intervention Type
Behavioral
Intervention Name(s)
Chronic care model for Bipolar Disorder
Intervention Description
The behavioral intervention is based on the Chronic Care Model (CCM) where patients receive information on managing bipolar symptoms and health habits in a group self-management session (up to 6 weekly sessions). The Care Manager then follows up with patients via phone contacts for 12 months following the intervention. The providers receive information on guidelines for care.
Primary Outcome Measure Information:
Title
Systolic and Diastolic Blood Pressure (SBP, DBP)
Description
24-month systolic and diastolic blood pressure (mm/Hg): lower is better
Time Frame
24 months
Title
Total Cholesterol
Description
Total cholesterol in mg/dl- lower is better
Time Frame
24 months
Title
Physical Health-related Quality of Life Score
Description
Physical health-related quality of life is based on the Short Form (SF)-12 survey physical health component (PCS) score- which ranges from 0 to 50, with higher scores indicating higher quality of life
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Manic Symptoms
Description
Manic symptoms based on the Internal State Scale (range is 0-500; higher score indicates more severe symptoms)
Time Frame
24 months
Title
Depressive Symptom Score
Description
Depressive symptoms based on the Internal State Scale (Range: 0-200, higher score = more severe symptoms)
Time Frame
24 months
Title
Disability Based on WHO-DAS Score
Description
Disability based on the WHO Disability Assessment Scale (WHO-DAS); range = 0-24, higher score equals greater disability
Time Frame
24 months
Title
Body Mass Index (BMI)
Description
Body mass index (BMI) is reported in kilograms divided by meters squared (kg/m^2) with a normal (healthy) range of 18-24, in which >=25 is considered overweight, and >=30 is the definition of obesity
Time Frame
24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of bipolar disorder (I, II, not otherwise specified, or schizoaffective-bipolar subtype) Have a diagnosis or be at risk for arteriosclerotic cardiovascular disease (ASCVD). We define this as a patient having a current diagnosis of or receiving treatment for at least one of the following medical conditions: hyperlipidemia or dyslipidemia (documented diagnosis or low-density lipoprotein >=160, or receiving statin or other treatment) hypertension (documented diagnosis or blood pressure of >=140/90 on 2 occasions) diabetes mellitus (documented diagnosis or HbA1C >=7%, or receiving treatment) obesity (documented diagnosis or BMI >30), based on medical record review of current problems current ASCVD diagnosis Exclusion Criteria: Have unresolved substance intoxication or withdrawal, such as appearing to be intoxicated (e.g., incoherent, slurred speech), or experiencing withdrawal symptoms from substance abuse at the time of enrollment. Are already enrolled in a mental health program with a mobile outreach component in which clinical caregivers deliver services to the patient in the community (e.g., assertive community treatment or intensive case management). These patients may be receiving similar services to those offered in the intervention. Are unwilling or unable to provide informed consent or comply with study requirements at the time of enrollment (e.g., unable to complete forms or attend scheduled sessions due to serious illness or substantial functional limitations).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amy M. Kilbourne, PhD MPH
Organizational Affiliation
VA Ann Arbor Healthcare System
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Ann Arbor Healthcare System
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48113
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23945460
Citation
Kilbourne AM, Goodrich DE, Lai Z, Post EP, Schumacher K, Nord KM, Bramlet M, Chermack S, Bialy D, Bauer MS. Randomized controlled trial to assess reduction of cardiovascular disease risk in patients with bipolar disorder: the Self-Management Addressing Heart Risk Trial (SMAHRT). J Clin Psychiatry. 2013 Jul;74(7):e655-62. doi: 10.4088/JCP.12m08082.
Results Reference
derived

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Self-Management Addressing Heart Disease Risk Trial

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