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Completed

NCT Number: NCT01542008

Treatment Adherence Enhancement in Bipolar Disorder

Bipolar disorder (BD) is a serious and chronic mental illness that is associated with substantial impairment in quality of life and functional outcomes, high rates of suicide, and high financial costs. In spite of a proliferation of treatments for BD, nearly half of individuals with BD do not benefit from pharmacotherapy because of sub-optimal medication treatment adherence. Non-adherence with BD medication treatment dramatically worsens outcomes. Reasons for non-adherence among individuals with BD are multi-dimensional, and it has been suggested that adherence enhancement might work best if the intervention specifically addresses factors that are important and modifiable for a specific individual. In spite of the enormity of the problem, the literature on interventions to improve treatment adherence is surprisingly limited. There is an urgent need for interventions to enhance treatment adherence among BD patients that: 1) are at high risk for future treatment non-adherence; 2) may not have access to or interest in long-term, high-intensity, and specialized care; and 3) are flexible and patient-focused taking into account reasons for non-adherence for a specific individual.

The proposed study is a first-ever RCT focused specifically on BD treatment adherence enhancement, and will test whether a customized adherence enhancement (CAE) psychosocial intervention improves adherence and mental health outcomes compared to broadly-directed, non-individualized education (EDU). The proposed project has the potential to greatly advance the care of BD patients who are at greatest risk for poor health outcomes, with findings expected to be generalizable across a variety of treatment settings.

Hypothesis 1: CAE will be associated with greater improvement in treatment adherence compared to broadly-directed, non-individualized BD education (EDU).

Hypothesis 2: CAE will be associated with improved BD symptoms compared to EDU.

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Key information

Conditions

Treatment Noncompliance Behavior Bipolar Disorder Bipolar and Related Disorders Health Behavior Mental Disorders Mood Disorders Patient Acceptance of Health Care Patient Compliance Treatment Adherence and Compliance

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospitals Case Medical Center

Cleveland, Ohio, 44106, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subjects must have type I or type II Bipolar Disorder (BD) as confirmed by the Structured Clinical Interview for DSM-IV Axis I Disorders Patient Version (SCID-P)
  • Have had BD for at least two years duration
  • Have received treatment with at least one evidence-based medication to stabilize mood for at least six months (lithium, anticonvulsant, or antipsychotic mood stabilizer)
  • Either 20% or more non-adherent with current BD medication treatment (i.e. lithium, anticonvulsant, or antipsychotic mood stabilizer)

Exclusion criteria

  • Unable or unwilling to participate in psychiatric interviews. This will include individuals, who may be too psychotic to participate in interviews/rating scales
  • Unable or unwilling to give written, informed consent to study participation
  • Individuals at high risk for suicide who can not be safely managed in their current treatment setting

Treatment and study plan

Customized Adherence Enhancement (CAE)

Behavioral

CAE consists of the application of a series of up to four psychosocial treatment modules based upon a baseline evaluation of adherence vulnerabilities/needs. The standardized modules (Psychoeducation, Modified Motivational Enhancement Therapy, Communication with Providers, Medication Routines), are assigned based upon pre-established criteria designed to fit the needs of the patient.

broadly-directed, non-individualized education (EDU)

Behavioral

EDU will consist of 4 core in-person sessions using the patient work-book from the NIMH funded study, Systematic Treatment Enhancement Program for Bipolar Disorder (STEP-BD), and following the general educational format of the Collaborative Care "control" intervention in the STEP study. EDU addresses BD treatment broadly, including diagnosis and management, and the sessions will review the materials and allow time for questions as needed.

Primary outcomes

  1. Change from baseline in the Tablet Routine Questionaire (TRQ) "past month" item at 24 weeks

    Time frame: Baseline and 24 weeks

    The TRQ "past month" item is a subject report of the percentage of prescribed medications not taken within the past month.

  2. Change from baseline in the Tablet Routine Questionaire (TRQ) "past week" item at 24 weeks

    Time frame: Baseline and 24 weeks

    The TRQ "past week" item is a subject report of the percentage of prescribed medications not taken within the past week.

  3. Change from baseline in treatment adherence as measured by special pill cap counter at 24 weeks

    Time frame: Baseline and 24 weeks

    A special pill cap will record the time/date of bottle opening. The cap will be used for the medication that the patient takes the most frequently (in the case of multiple BD medications taken at same frequency, the medication that was started most recently will be selected). A dose will be counted as "taken" if the bottle is opened within two hours of the prescribed time. A percent of doses taken (treatment adherence) will be calculated by dividing the number of times the bottle is opened by the number of times it should have been opened as per the prescription.

Secondary outcomes

  1. Change from baseline in Brief Psychiatry Symptom Scale (BPRS) at 24 weeks

    Time frame: baseline and 24 weeks

  2. Change from baseline in Montgomery Asberg Depression Rating Scale (MADRS) at 24 weeks

    Time frame: baseline and 24 weeks

  3. Change from baseline in Young Mania Rating Scale (YMRS) at 24 weeks

    Time frame: baseline and 24 weeks

  4. Change from baseline in Clinical Global Impression, Bipolar Version (CGI-BP) at 24 weeks

    Time frame: baseline and 24 weeks

  5. Change from baseline in Global Assessment of Functioning (GAF) at 24 weeks

    Time frame: baseline and 24 weeks

  6. Change from baseline in General Self Efficacy Scale at 24 weeks

    Time frame: baseline and 24 weeks

  7. Change from baseline in the Drug and Alcohol portion of the Addiction Severity Index (ASI) at 24 weeks

    Time frame: baseline and 24 weeks

  8. Change from baseline in Treatment alliance (Trust in Providers scale) at 24 weeks

    Time frame: baseline and 24 weeks

  9. Change from baseline in Stigma for Mental Illness Scale at 24 weeks

    Time frame: baseline and 24 weeks

  10. Change from baseline in Drug Attitudes Inventory (DAI) at 24 weeks

    Time frame: baseline and 24 weeks

Sponsors and collaborators

Lead sponsor

Case Western Reserve University

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Acronym: CAE RCT

Important dates

Study start
2012
Primary completion
2017
Study completion
2017
First posted
Mar 1, 2012
Registry last updated
Dec 14, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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