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Customized Medication Adherence Enhancement for Treating Adults With Bipolar Disorder

Primary Purpose

Bipolar Disorder

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Psychoeducation module
Substance abuse module
Improved communication/rapport with provider module
Medication routines management module
Sponsored by
Case Western Reserve University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Disorder focused on measuring Patient Non-Adherence, Patient Non-Compliance, Patient Nonadherence, Patient Noncompliance, Patient Refusal of Treatment, Refusal of Treatment, Treatment Refusal

Eligibility Criteria

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

Inclusion Criteria:

  • Clinical diagnosis of bipolar disorder (BPD) Type I or Type II, as determined by a standardized diagnostic interview, the Mini-International Neuropsychiatric Interview (MINI)
  • Demonstrated history of poor medication adherence, as determined by self-report or clinician report. In this study, self-reported treatment nonadherence will be identified with the Tablet Routines Questionnaire (TRQ). Poorly adherent individuals will be defined as those who miss 30% or more of medication within either the past week or past month (those missing 30% or more within past week will be considered to be nonadherent over the past month). Clinician-assessed nonadherence will be identified via a clinician version of the TRQ to identify nonadherence of 30% or more over the past 30 days.
  • BPD of at least 2 years' duration
  • Treatment with medication to stabilize mood for at least 6 months

Exclusion Criteria:

  • Unable/unwilling to participate in psychiatric interviews, as based on the clinical opinion of the investigator or the treating clinician
  • High risk of suicide, as seen in factors such as active suicidal ideation, recent suicide attempt, or current intent or plan
  • Inability to speak English
  • Individuals who have participated in Project 1, Personal Adherence Evaluation of Individuals Receiving Treatment for Bipolar Disorder (PAE in BD)

Sites / Locations

  • Connections

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Customized Adherence Enhancement (CAE)

Arm Description

Participants, all of whom have a history of medication nonadherence, will be assigned to one or more treatment modules based on their individual profiles. Treatment Modules: Psychoeducation module Substance abuse module Improved communication/rapport with provider module Medication routines management module

Outcomes

Primary Outcome Measures

Change in Treatment Adherence Within the Past Month as Measured by the Tablet Routines Questionnaire
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.
Change in Treatment Adherence Within the Past Week as Measured by the Tablet Routines Questionnaire
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.
Change in Treatment Adherence as Measured by the Morisky Scale
The minimum score is 0 and the maximum score is 4. A higher score implies poorer treatment adherence.
Change in Treatment Adherence Within the Past Month as Measured by the Tablet Routines Questionnaire
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.
Change in Treatment Adherence Within the Past Week as Measured by the Tablet Routines Questionnaire
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.

Secondary Outcome Measures

Change in Attitude as Measured by the Attitude Toward Mood Stabilizers Questionnaire (AMSQ)
The AMSQ is a modification of the Lithium Attitudes Questionnaire. The minimum score is 0 and the maximum score is 19. A higher score implies a poorer attitude.
Change in Attitude as Measured by the Rating of Medication Influences (ROMI)
The minimum score is 0 and the maximum score is 10. A higher score implies a poorer attitude.
Change in Depression as Measured by the Hamilton Rating Scale for Depression (HAM-D)
The minimum score is 0 and the maximum score is 52. A higher score implies a worse condition.
Change in Symptoms of Bipolar Disorder as Measured by the Young Mania Rating Scale (YMRS)
The minimum score is 0 and the maximum score is 60. A higher score implies a worse condition.
Change in Symptoms of Bipolar Disorder as Measured by the Brief Psychiatric Rating Scale (BPRS)
The minimum score is 18 and the maximum score is 126. A higher score implies a worse condition.
Change in Global Psychopathology as Measured by the Clinical Global Impression for Bipolar Disorder (CGI-BP)
The minimum score is 1 and the maximum score is 7. A higher score implies a worse condition.
Change in Functional Status as Measured by the Global Assessment of Functioning (GAF) Scale
The minimum score is 1 and the maximum score is 100. A higher score implies higher functioning.
Change in Perception of Physical Health as Measured by the 12-item Short Form Health Survey (SF-12)
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived physical health.
Change in Perception of Mental Health as Measured by the 12-item Short Form Health Survey (SF-12)
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived mental health.
Change in Depression as Measured by the Hamilton Rating Scale for Depression (HAM-D)
The minimum score is 0 and the maximum score is 52. A higher score implies a worse condition.
Change in Symptoms of Bipolar Disorder as Measured by the Young Mania Rating Scale (YMRS)
The minimum score is 0 and the maximum score is 60. A higher score implies a worse condition.
Change in Symptoms of Bipolar Disorder as Measured by the Brief Psychiatric Rating Scale (BPRS)
The minimum score is 18 and the maximum score is 126. A higher score implies a worse condition.
Change in Global Psychopathology as Measured by the Clinical Global Impression for Bipolar Disorder (CGI-BP)
The minimum score is 1 and the maximum score is 7. A higher score implies a worse condition.
Change in Functional Status as Measured by the Global Assessment of Functioning (GAF) Scale
The minimum score is 1 and the maximum score is 100. A higher score implies higher functioning.
Change in Attitude as Measured by the Attitude Toward Mood Stabilizers Questionnaire (AMSQ)
The AMSQ is a modification of the Lithium Attitudes Questionnaire. The minimum score is 0 and the maximum score is 19. A higher score implies a poorer attitude.
Change in Attitude as Measured by the Rating of Medication Influences (ROMI)
The minimum score is 0 and the maximum score is 10. A higher score implies a poorer attitude.
Change in Perception of Physical Health as Measured by the 12-item Short Form Health Survey (SF-12)
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived physical health.
Change in Perception of Mental Health as Measured by the 12-item Short Form Health Survey (SF-12)
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived physical health.

Full Information

First Posted
September 29, 2008
Last Updated
October 9, 2014
Sponsor
Case Western Reserve University
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00763919
Brief Title
Customized Medication Adherence Enhancement for Treating Adults With Bipolar Disorder
Official Title
Customized Adherence Enhancement in Bipolar Disorder (CAE in BD)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2014
Overall Recruitment Status
Completed
Study Start Date
July 2008 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
October 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Case Western Reserve University
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In this study, patients with bipolar disorder who do not take their medications as prescribed will receive specialized education and therapy treatment to determine whether the specialized treatment is effective in helping patients to take their medications consistently.
Detailed Description
Bipolar disorder (BPD) is a chronic disorder characterized by manic and depressive episodes that disrupt healthy, functional lives. Despite recent advances in medication treatments, many BPD patients do not take their medications. Medication nonadherence is associated with multiple risks, such as relapse, rehospitalization, lengthier hospital stays, and, in some cases, increased risk of suicide. Some studies have shown that treatment adherence in BPD can be improved, particularly through psychological education, development of self-management strategies or behaviors, and ongoing relapse prevention. This study will examine the effectiveness of medication adherence treatment modules specialized to deal with specific reasons for nonadherence. Participants, all of whom have a history of medication nonadherence, will undergo structured interviews and complete self-report questionnaires to determine individual reasons for nonadherence. Based on their individual profiles, participants will be assigned to one or more of the following intervention modules: Psychoeducation: This module uses education about BPD and related treatment to address patient issues such as opposition to preventive efforts, denial of the need for or effectiveness of medication, negative attitudes toward drugs in general, lack of information about mood stabilizers, and stigma or embarrassment related to BPD treatment. Substance abuse: This module targets substance abuse problems that interfere with medication adherence. Communication with providers: This module addresses fear of medication side effects by improving communication with health care providers. Medication routines management: This module addresses difficulties establishing a medication routine and outside opposition to medications by developing strategies for consistent medication adherence routines. Each module will involve four 60-minute sessions conducted in a 4- to 6-week period. The study therapist will conduct each of these sessions individually with the participant, combining or coadministering modules in a single session if participants are assigned to more than one module. Depending on which module or modules participants are assigned to, they may also be contacted by phone one to three times by the therapist to complete all module materials. This study will be conducted in two phases. In the first, an initial group of participants will undergo the module treatments and then participants and therapists will be interviewed about the effectiveness and feasibility of the interventions. This feedback will be used to refine the modules. In the second phase, a second group of participants will undergo treatment in the refined modules and provide more feedback. All participants will continue with their regular treatment while undergoing module treatments. Participation in this study will last 4 to 6 weeks, with follow-up interviews and assessments ending 6 months after completion of the intervention. In all, there will be five assessments, completed at an initial screening visit, just before treatment, just after treatment, and 3 and 6 months after the completion of treatment. The initial assessments will last 60 to 90 minutes and involve questionnaires and a structured interview. The other four assessments will last 45 to 60 minutes. Treatment adherence, attitudes toward medications, BPD symptoms, and overall functioning will be measured at each assessment. The number of pills used in each participant's prescription bottles will also be counted as a measure of medication adherence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Disorder
Keywords
Patient Non-Adherence, Patient Non-Compliance, Patient Nonadherence, Patient Noncompliance, Patient Refusal of Treatment, Refusal of Treatment, Treatment Refusal

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
43 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Customized Adherence Enhancement (CAE)
Arm Type
Experimental
Arm Description
Participants, all of whom have a history of medication nonadherence, will be assigned to one or more treatment modules based on their individual profiles. Treatment Modules: Psychoeducation module Substance abuse module Improved communication/rapport with provider module Medication routines management module
Intervention Type
Behavioral
Intervention Name(s)
Psychoeducation module
Intervention Description
The psychoeducation module will use psychological and medication education to address opposition to prophylaxis, denial of illness severity or therapeutic effectiveness, negative attitudes toward drugs in general, lack of information about mood stabilizers, and stigma or embarrassment over medications or in relation to the use of complementary or alternative treatments.
Intervention Type
Behavioral
Intervention Name(s)
Substance abuse module
Intervention Description
The substance abuse module will address problematic substance abuse, particularly as it relates to medication adherence.
Intervention Type
Behavioral
Intervention Name(s)
Improved communication/rapport with provider module
Intervention Description
The provider communication and rapport module will improve health care provider communication to address fear of side effects, concern regarding change in appearance, or side effect-related distress.
Intervention Type
Behavioral
Intervention Name(s)
Medication routines management module
Intervention Description
The medication routines management module will develop strategies and behaviors that help create medication adherence routines for those who have difficulties with medication routines or experience outside opposition to medications.
Primary Outcome Measure Information:
Title
Change in Treatment Adherence Within the Past Month as Measured by the Tablet Routines Questionnaire
Description
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.
Time Frame
baseline and 6 months
Title
Change in Treatment Adherence Within the Past Week as Measured by the Tablet Routines Questionnaire
Description
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.
Time Frame
baseline and 6 months
Title
Change in Treatment Adherence as Measured by the Morisky Scale
Description
The minimum score is 0 and the maximum score is 4. A higher score implies poorer treatment adherence.
Time Frame
baseline and 6 months
Title
Change in Treatment Adherence Within the Past Month as Measured by the Tablet Routines Questionnaire
Description
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.
Time Frame
baseline and 3 months
Title
Change in Treatment Adherence Within the Past Week as Measured by the Tablet Routines Questionnaire
Description
The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.
Time Frame
baseline and 3 months
Secondary Outcome Measure Information:
Title
Change in Attitude as Measured by the Attitude Toward Mood Stabilizers Questionnaire (AMSQ)
Description
The AMSQ is a modification of the Lithium Attitudes Questionnaire. The minimum score is 0 and the maximum score is 19. A higher score implies a poorer attitude.
Time Frame
baseline and 6 months
Title
Change in Attitude as Measured by the Rating of Medication Influences (ROMI)
Description
The minimum score is 0 and the maximum score is 10. A higher score implies a poorer attitude.
Time Frame
baseline and 6 months
Title
Change in Depression as Measured by the Hamilton Rating Scale for Depression (HAM-D)
Description
The minimum score is 0 and the maximum score is 52. A higher score implies a worse condition.
Time Frame
baseline and 6 months
Title
Change in Symptoms of Bipolar Disorder as Measured by the Young Mania Rating Scale (YMRS)
Description
The minimum score is 0 and the maximum score is 60. A higher score implies a worse condition.
Time Frame
baseline and 6 months
Title
Change in Symptoms of Bipolar Disorder as Measured by the Brief Psychiatric Rating Scale (BPRS)
Description
The minimum score is 18 and the maximum score is 126. A higher score implies a worse condition.
Time Frame
baseline and 6 months
Title
Change in Global Psychopathology as Measured by the Clinical Global Impression for Bipolar Disorder (CGI-BP)
Description
The minimum score is 1 and the maximum score is 7. A higher score implies a worse condition.
Time Frame
baseline and 6 months
Title
Change in Functional Status as Measured by the Global Assessment of Functioning (GAF) Scale
Description
The minimum score is 1 and the maximum score is 100. A higher score implies higher functioning.
Time Frame
baseline and 6 months
Title
Change in Perception of Physical Health as Measured by the 12-item Short Form Health Survey (SF-12)
Description
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived physical health.
Time Frame
baseline and 6 months
Title
Change in Perception of Mental Health as Measured by the 12-item Short Form Health Survey (SF-12)
Description
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived mental health.
Time Frame
baseline and 6 months
Title
Change in Depression as Measured by the Hamilton Rating Scale for Depression (HAM-D)
Description
The minimum score is 0 and the maximum score is 52. A higher score implies a worse condition.
Time Frame
baseline and 3 months
Title
Change in Symptoms of Bipolar Disorder as Measured by the Young Mania Rating Scale (YMRS)
Description
The minimum score is 0 and the maximum score is 60. A higher score implies a worse condition.
Time Frame
baseline and 3 months
Title
Change in Symptoms of Bipolar Disorder as Measured by the Brief Psychiatric Rating Scale (BPRS)
Description
The minimum score is 18 and the maximum score is 126. A higher score implies a worse condition.
Time Frame
baseline and 3 months
Title
Change in Global Psychopathology as Measured by the Clinical Global Impression for Bipolar Disorder (CGI-BP)
Description
The minimum score is 1 and the maximum score is 7. A higher score implies a worse condition.
Time Frame
baseline and 3 months
Title
Change in Functional Status as Measured by the Global Assessment of Functioning (GAF) Scale
Description
The minimum score is 1 and the maximum score is 100. A higher score implies higher functioning.
Time Frame
baseline and 3 months
Title
Change in Attitude as Measured by the Attitude Toward Mood Stabilizers Questionnaire (AMSQ)
Description
The AMSQ is a modification of the Lithium Attitudes Questionnaire. The minimum score is 0 and the maximum score is 19. A higher score implies a poorer attitude.
Time Frame
baseline and 3 months
Title
Change in Attitude as Measured by the Rating of Medication Influences (ROMI)
Description
The minimum score is 0 and the maximum score is 10. A higher score implies a poorer attitude.
Time Frame
baseline and 3 months
Title
Change in Perception of Physical Health as Measured by the 12-item Short Form Health Survey (SF-12)
Description
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived physical health.
Time Frame
baseline and 3 months
Title
Change in Perception of Mental Health as Measured by the 12-item Short Form Health Survey (SF-12)
Description
The minimum score is 1 and the maximum score is 99. A higher score implies higher perceived physical health.
Time Frame
baseline and 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of bipolar disorder (BPD) Type I or Type II, as determined by a standardized diagnostic interview, the Mini-International Neuropsychiatric Interview (MINI) Demonstrated history of poor medication adherence, as determined by self-report or clinician report. In this study, self-reported treatment nonadherence will be identified with the Tablet Routines Questionnaire (TRQ). Poorly adherent individuals will be defined as those who miss 30% or more of medication within either the past week or past month (those missing 30% or more within past week will be considered to be nonadherent over the past month). Clinician-assessed nonadherence will be identified via a clinician version of the TRQ to identify nonadherence of 30% or more over the past 30 days. BPD of at least 2 years' duration Treatment with medication to stabilize mood for at least 6 months Exclusion Criteria: Unable/unwilling to participate in psychiatric interviews, as based on the clinical opinion of the investigator or the treating clinician High risk of suicide, as seen in factors such as active suicidal ideation, recent suicide attempt, or current intent or plan Inability to speak English Individuals who have participated in Project 1, Personal Adherence Evaluation of Individuals Receiving Treatment for Bipolar Disorder (PAE in BD)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Martha Sajatovic, MD
Organizational Affiliation
Case Western Reserve University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Connections
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44122
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Customized Medication Adherence Enhancement for Treating Adults With Bipolar Disorder

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