Telemedicine for Women With Anhedonia in Bipolar and Unipolar Disorder
Primary Purpose
Depression, Bipolar Disorder, Anhedonia
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Behavioral Activation-Full
Behavioral Activation-Short
Bipolar Disorder Collaborative Care
Sponsored by

About this trial
This is an interventional treatment trial for Depression focused on measuring Depression, Bipolar Disorder, Anhedonia, Women
Eligibility Criteria
Inclusion Criteria:
- Currently experiencing a score ≥ 20 on a clinician-administered scale of anhedonia
- Currently experiencing two or more symptoms of depression with bipolar disorder either Type I or II (one of these symptoms should be anhedonia) OR
- Currently experiencing two or more symptoms of unipolar depression, without current psychotic features (one of these symptoms should be anhedonia)
- Currently on a medication for a mood disorder
- Proficiency in English
- Able to provide informed consent
Exclusion Criteria:
- Current psychosis (schizoaffective, schizophreniform, delusional disorder)
- Current suicide risk sufficient to preclude treatment on an outpatient basis
- Severe, unstable concurrent psychiatric conditions likely to require hospitalization within six months (ex. hazardous substance use evidenced by a score > 10 on the Alcohol Use Disorders Identification Test or > 2 on the Drug Use Disorders identification Test)
- Current incarcerated or on probation due to criminal allegations
- Currently pregnant
- Cognitive impairment
- Those living in the United States on a VISA
- Those currently in psychotherapy
Sites / Locations
- Northwestern University
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Active Comparator
Arm Label
Behavioral Activation-Full
Behavioral Activation-Short
Bipolar Disorder Collaborative Care
Arm Description
Twelve weekly sessions of phone therapy using Behavioral Activation Treatment for Anhedonia.
Eight weekly sessions of phone therapy using Behavioral Activation Treatment for Anhedonia.
Twelve weekly sessions of phone therapy using BDCC manual adapted for anhedonia.
Outcomes
Primary Outcome Measures
Snaith-Hamilton Pleasure Scale-Clinician Version
Clinician-administered measure of anhedonia spanning the domains of: interests, social interaction, sensory experience, and food/drink.
Secondary Outcome Measures
Inventory of Depressive Symptomatology-Clinician
Clinician-administered measure of depression severity
Clinician-Administered Rating Scale for Mania
Clinician-administered measure of the severity of manic symptoms which includes items that focus on Bipolar and items that focus on psychosis
Full Information
NCT ID
NCT02494050
First Posted
June 30, 2015
Last Updated
September 28, 2016
Sponsor
Northwestern University
1. Study Identification
Unique Protocol Identification Number
NCT02494050
Brief Title
Telemedicine for Women With Anhedonia in Bipolar and Unipolar Disorder
Official Title
Telemedicine for Women With Anhedonia in Bipolar and Unipolar Disorder: Patient Preferences and Outcomes
Study Type
Interventional
2. Study Status
Record Verification Date
September 2016
Overall Recruitment Status
Completed
Study Start Date
June 2015 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Anhedonia, characterized as (a) the diminished motivation to participate in activities, and/or (b) diminished enjoyment of a pleasurable activity are common symptoms among women diagnosed with mood disorders. This trial aims to test three treatments adapted to reduce anhedonia.
The investigators will compare three treatment groups, specifically, two doses of Behavioral Activation treatment for anhedonia (i.e., 12 weeks vs. 8 weeks of BA) with an active comparator treatment, Bipolar Disorder Collaborative Care (12 weeks of BDCC). BA is a psychotherapy approach that helps participants to identify and modify environmental sources of their depression. BDCC is a supportive care approach that educates participants to optimize their medication initiation or their existing medication regimen. The time frame for this study will be between 12-14 weeks. Specifically, participants will be evaluated and enrolled within one week, then received up to 12 weeks of treatment (tracked through this time) and then complete two evaluations (one at week 8) and another at the end of treatment (an expected average of 12-14 weeks after enrolling into treatment).
Primary analyses aim to compare the dose-mechanism change in BA relative to a standard medication optimizing protocol, BDCC. The secondary analyses are to evaluate individual differences in stated patient preferences for treatment, and group differences in treatment effect on anhedonia, side effects, and quality of life.
Detailed Description
Prospective volunteers will be screened by phone and, if eligible, invited to a clinical evaluation in the laboratory, located at Northwestern University. At the laboratory, prospective volunteers complete written informed consent and learn about the study.
All evaluations will measure the following variables: Anhedonia will be assessed using the Snaith-Hamilton Pleasure Scale, Temporal Experience of Pleasure Scale, and Effort-Expenditure for Rewards Task; Mood symptoms will be assessed by the Structured Clinical Interview for DSM-IV, Inventory of Depressive Symptomatology-Clinician Version, Clinician-Administered Rating Scale for Mania, Inventory of Depressive Symptomatology-Clinician version, and Columbia Suicide Severity Rating Scale. Treatment preferences will measured with the Stated Preferences Inventory for Bipolar Disorder. The presence of side effects from medications will be evaluated using the Frequency, Intensity, and Burden of Side Effects measure. Maternal function will be evaluated using the Barkin Index of Maternal Function self-report. Behavioral Inhibition System/Behavioral Activation System and the Behavioral Activation for Depression Scale are used to evaluate activation levels. Reward processing will be measured using the Monetary Incentive Delay Task on the computer and the Reward Probability Index questionnaire.
Enrollment is determined on a set of criteria, whereby participants will be randomized into one of three treatment groups using a computerized randomized number generator using a 1:1:1 ratio. Allocation concealment will be set up so the person enrolling the participant will not know in advance which treatment the participant will receive. Moreover, evaluators will remain blind to treatment assignment. Participants are randomized to receive one of three treatments: 12 weeks of BA, 8 weeks of BA with option to add 4 weeks, and 12 weeks of BDCC. Participants are asked to participate in two follow-up evaluations at the laboratory, scheduled at Weeks 8 and 12. The study ends after the Week 12 evaluation (approximately 12-14 weeks after enrolling into the treatment).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Bipolar Disorder, Anhedonia
Keywords
Depression, Bipolar Disorder, Anhedonia, Women
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
17 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Behavioral Activation-Full
Arm Type
Experimental
Arm Description
Twelve weekly sessions of phone therapy using Behavioral Activation Treatment for Anhedonia.
Arm Title
Behavioral Activation-Short
Arm Type
Experimental
Arm Description
Eight weekly sessions of phone therapy using Behavioral Activation Treatment for Anhedonia.
Arm Title
Bipolar Disorder Collaborative Care
Arm Type
Active Comparator
Arm Description
Twelve weekly sessions of phone therapy using BDCC manual adapted for anhedonia.
Intervention Type
Behavioral
Intervention Name(s)
Behavioral Activation-Full
Intervention Description
Behavioral Activation proposes that symptom reduction occurs via monitoring daily activities to identify patterns of low reward and mood, assessing and assigning tasks that generate pleasure and competence, understanding and reducing unproductive avoidance, and improving skill deficits to promote action towards treatment goals.
Intervention Type
Behavioral
Intervention Name(s)
Behavioral Activation-Short
Intervention Description
Behavioral Activation proposes that symptom reduction occurs via monitoring daily activities to identify patterns of low reward and mood, assessing and assigning tasks that generate pleasure and competence, understanding and reducing unproductive avoidance, and improving skill deficits to promote action towards treatment goals.
Intervention Type
Behavioral
Intervention Name(s)
Bipolar Disorder Collaborative Care
Intervention Description
This manualized treatment focuses on social support and educating patients about medication compliance. The primary focus is to strengthen the patients' self-management skills with education; supporting the clinician's decision making using practice guidelines; enhancing access to care, continuity of care, and information flow through the use of the clinician.
Primary Outcome Measure Information:
Title
Snaith-Hamilton Pleasure Scale-Clinician Version
Description
Clinician-administered measure of anhedonia spanning the domains of: interests, social interaction, sensory experience, and food/drink.
Time Frame
approximately 12-14 weeks after enrolling into the treatment
Secondary Outcome Measure Information:
Title
Inventory of Depressive Symptomatology-Clinician
Description
Clinician-administered measure of depression severity
Time Frame
approximately 12-14 weeks after enrolling into the treatment
Title
Clinician-Administered Rating Scale for Mania
Description
Clinician-administered measure of the severity of manic symptoms which includes items that focus on Bipolar and items that focus on psychosis
Time Frame
approximately 12-14 weeks after enrolling into the treatment
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Currently experiencing a score ≥ 20 on a clinician-administered scale of anhedonia
Currently experiencing two or more symptoms of depression with bipolar disorder either Type I or II (one of these symptoms should be anhedonia) OR
Currently experiencing two or more symptoms of unipolar depression, without current psychotic features (one of these symptoms should be anhedonia)
Currently on a medication for a mood disorder
Proficiency in English
Able to provide informed consent
Exclusion Criteria:
Current psychosis (schizoaffective, schizophreniform, delusional disorder)
Current suicide risk sufficient to preclude treatment on an outpatient basis
Severe, unstable concurrent psychiatric conditions likely to require hospitalization within six months (ex. hazardous substance use evidenced by a score > 10 on the Alcohol Use Disorders Identification Test or > 2 on the Drug Use Disorders identification Test)
Current incarcerated or on probation due to criminal allegations
Currently pregnant
Cognitive impairment
Those living in the United States on a VISA
Those currently in psychotherapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jackie K Gollan, Ph.D.
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwestern University
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Telemedicine for Women With Anhedonia in Bipolar and Unipolar Disorder
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