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Internet-Based Interventions for Bipolar Disorder

Not Applicable
Conditions
Bipolar Disorder
Interventions
Behavioral: Moderated Discussion Board
Behavioral: Psychoeducation
Behavioral: Interactive Psychosocial Tools
Registration Number
NCT02106078
Lead Sponsor
VA Palo Alto Health Care System
Brief Summary

The investigators hope to learn whether access to online support and education can help people with Bipolar Disorder (BD) better manage their symptoms of depression.

Detailed Description

This study will examine if there is a benefit of an online intervention for persons with bipolar diagnoses, and what components appear to be useful. Specifically, the study will examine (1) whether exposure to the MoodSwings 2.0 intervention results in decreased depressive symptoms as measured by the Montgomery Asberg Rating Scale for Depression (MADRS) and (2) whether there is an association between graduated levels of involvement (Level I, 2, or 3) and resulting improvement? We expect that those participants assigned to the control condition (Level 1, peer discussion board only), will have fewer positive outcomes than those in Level 2 (discussion board and psychoeducation) or 3 (discussion board, psychoeducation, and interactive psychosocial tools) conditions.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
300
Inclusion Criteria
  • Current diagnosis of bipolar I disorder, bipolar II disorder, or bipolar disorder NOS verified with the Structured Clinical Interview for the Diagnostic and Statistical Manual for Mental Disorders (SCID) Mood disorder module.
  • Age 21-65.
  • Access to a computer with internet access. Access to a printer is preferable, but not required.
  • Able to speak and read English proficiently.
  • Some degree of medical supervision of bipolar disorder (sees a health professional at least twice a year to discuss symptoms and treatment needs) and local access to emergency care.
Exclusion Criteria
  • Current psychosis, as assessed in screening phone interview with the SCID psychosis module.
  • Acutely suicidal (defined as having a HAM-D item 3, score of ≥3).
  • Current mania, assessed using mania module of the SCID mood disorders module.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Level 2Moderated Discussion BoardModerated discussion board plus psychoeducation
Level 3PsychoeducationModerated discussion board plus psychoeducation plus interactive psychosocial tools
Level 3Moderated Discussion BoardModerated discussion board plus psychoeducation plus interactive psychosocial tools
Level 1Moderated Discussion BoardModerated discussion board only
Level 2PsychoeducationModerated discussion board plus psychoeducation
Level 3Interactive Psychosocial ToolsModerated discussion board plus psychoeducation plus interactive psychosocial tools
Primary Outcome Measures
NameTimeMethod
Montgomery Asberg Rating Scale (MADRS) for DepressionChange from Baseline to 3 months, 6 months, 9 months and 12 months

The MADRS is a 10-item scale, completed by the clinician to assess symptoms of depression. It is particularly sensitive to changes in depression over time. Joint reliability for the total score across several studies ranged from 0.76 to 0.95, and it is viewed as a reliable and valid measure of depression symptoms.

Young Mania Rating ScaleChange from Baseline to 3 months, 6 months, 9 months and 12 months

The YMRS is an 11-item scale, completed by the clinician to assess symptoms of mania. This scale is viewed as a reliable and valid measure of manic symptoms, and is sensitive to changes in mania over time.

Secondary Outcome Measures
NameTimeMethod
Time to Intervention for Mood Episode( TIME)Changes from Baseline to 3 months, 6 months, 9 months and 12 months

Relapse or time to intervention will be assessed using Time Scale , with intervention defined as initiation, discontinuation, or dose adjustment of a treatment, initiation of psychotherapy or ECT, visit to an emergency provider or hospitalization in response to new mood symptoms.

SF-12Change from Baseline to 3 months, 6 months, 9 months and 12 months

The SF-12 is a short, multipurpose measure of perceived impairment due to health problems. It is widely used as a short version of the SF-36, and has good validity. The SF-12 yields two risk-adjusted summary scores, impairment perceived as due to physical illness and impairment perceived as due to emotional problems (Ware et al., 1996)

Cornell Service Index (CSI)Change from Baseline to 3 months, 6 months, 9 months and 12 months

Use of general medical and psychiatric health services will be collected via the Cornell Service Index (CSI; Sirey et al., 2005). The CSI is a brief assessment of health service use. It has good inter-rater and test-retest reliability and assesses four types of services: outpatient psychiatric or psychological services (e.g., psychotropic medication visits or psychotherapy), outpatient medical services (e.g., visits to medical providers), professional support services (e.g., home health nurse visits, meal delivery), and intensive services (e.g., emergency department visits or hospitalization).

Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q)Change from baseline to 3 months, 6 months, 9 months and 12 months

The Quality of Life, Enjoyment and Satisfaction Questionnaire (Q-LES-Q) assesses subjective quality of life(i.e. physical health, subjective feelings, leisure activities and and social relationships). The 16 item short form is designated to measure satisfaction with various areas of daily functioning, such as social relationships, living/housing, physical heath, medication and global satisfaction.

Medication Adherence rating Scale( MARS)Changes from Baseline to 3 months, 6months, 9 months and 12 months

When applicable, adherence to prescribed medication will be assessed with the Medication Adherence Rating Scale(MARS). This 10-item scale has acceptable reliability, with Cronbach's alpha.75, and test re-test reliability 0.72. It is seen as a valid measure with significant correlations with other measures of medication adherence(p\<.01) and with serum blood levels at p\< .05.

Patient satisfaction Questionnaire 18( PSQ-18)Changes from Baseline to 3 months, 6 months, 9 months and 12 months

The Patient satisfaction Questionnaire 18 assesses the overall satisfaction of each participant with their current medical care. This 18-item scale is a short form version of the 50-item Patient satisfaction Questionnaire. The PSQ sub-scales show acceptable internal consistency reliability. Furthermore, corresponding PSQ 18 and PSQIII subscales are substantially correlated with one another.

Treatment Satisfaction Questionnaire- ModifiedChanges from Baseline to 3 months, 6 months, 9 months and 12 months

For the purposes of this study, the Treatment satisfaction Questionnaire- Modified was revised to suit the bipolar disorder and the MoodSwings 2.0 Program. This questionnaire was originally a modified version of the Treatment Satisfaction Questionnaire

Medical Outcomes Study Social Support Survey( MOS-SSS)Changes from Baseline to 3 months, 6 months, 9 months and 12 months

Social support will be assessed with the Medical Outcomes Study Social Support Survey. This 18-item scale has acceptable reliability( alpha \> 0.91) and construct validity, and was specifically developed for people with chronic conditions.

Trial Locations

Locations (1)

VA Palo Alto Healthcare System

🇺🇸

Palo Alto, California, United States

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