CAE Plus LAI in Individuals With Bipolar Disorder at Risk for Treatment Non-adherence (BD-CAEL)

Phase 4

Completed

Conditions: Medication Non Adherence
Medication Adherence
Bipolar Disorder

Interventions: Drug: Abilify Maintena
Behavioral: Customized Adherence Enhancement (CAE)

Registration Number: NCT03408873

Lead Sponsor: Martha Sajatovic

Brief Summary: This is a prospective study using customized adherence enhancement (CAE) and long-acting injectable (LAI) antipsychotic in 30 individuals with bipolar disorder (BD) at risk for treatment non-adherence. The CAE approach is expected to improve treatment adherence, as well as improve BD symptoms, functioning and treatment attitudes among subjects with bipolar disorder.

Detailed Description: Oral Abilify (aripiprazole) is effective in the treatment of patients with BD when prescribed as an acute anti-manic agent and for the maintenance treatment of bipolar disorder. Abilify Maintena is an intramuscular (IM) depot formulation of oral aripiprazole (Abilify). Abilify Maintena appears to be as effective as standard oral Abilify and may maximize patient adherence. Recent clinical trials suggest that Abilify Maintena is effective for the treatment of patients with BD.

Customized Adherence Enhancement (CAE) is a brief behavioral intervention that improves adherence approximately 30% more than an educational control in adults with BD. The CAE program is a brief, practical intervention consisting of a series of up to four psychosocial treatment modules based upon an adult's unique adherence barriers: 1) Psychoeducation on BD Medications; 2) Communication with Providers; 3) Strategies to Enhance Medication Routines; and 4) Targeting Substance Use Problems with Modified Motivational Enhancement Therapy. Multiple studies conducted by these investigators has shown that CAE is effective in in treating poorly adherent BD adults.

In addition, studies by these investigators have shown that combining LAI + CAE dramatically improves adherence, symptoms and functional outcomes in people with schizophrenia and schizoaffective disorder. In summary, LAI can maximize medication adherence, while CAE addresses individual barriers to sustained adherence and behavioral change. Combining LAI + CAE improves adherence, symptoms and functioning in high-risk people with primary psychotic disorders. The proposed project will test the efficacy of combining Abilify Maintena with CAE to help improve outcomes in poorly adherent patients with BD. Pilot data suggest that adherence with concomitantly prescribed psychotropic drugs improves with LAI + CAE. The findings have particular relevance to BD because many BD patients are on concomitant oral psychotropic drugs in addition to antipsychotic. Thus, it is expected that combining CAE with LAI will lead to a "halo effect" in that these BD patients will engage in their own care more broadly.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 30

Inclusion Criteria

Individuals age 18 and older with BD Type 1 or 2 as confirmed by the Mini International Psychiatric Inventory (MINI).
Known to have medication treatment adherence problems as identified by the Treatment Routines Questionnaire (TRQ, 20% or more missed medications in past week or past month)
Screening the Brief Psychiatric Rating Scale (BPRS) score of ≥ 36
Ability to be rated on psychiatric rating scales.
Willingness to take long-acting injectable antipsychotic medication (LAI)
Currently in treatment or scheduled to receive treatment at a Community Mental Health Clinic (CMHC) or other clinical setting able to provide mental health care during and after study participation
Able to provide written, informed consent to study participation.

Exclusion Criteria

Individuals on LAI immediately prior to study enrollment.
Individuals with known intolerance or resistance to either oral aripiprazole or LAI formulation of aripiprazole
Prior or current treatment with clozapine
Medical condition or illness, which in the opinion of the research psychiatrist, would interfere with the patient's ability to participate in the trial
Physical dependence on substances (alcohol or illicit drugs) likely to lead to withdrawal reaction during the course of the study in the clinical opinion of the treated research psychiatrist
Immediate risk of harm to self or others
Female who is currently pregnant or breastfeeding

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Patient Noncompliance	Abilify Maintena	Subjects enrolled in the study will receive both Abilify Miantena and the Customized Adherence Enhancement (CAE) intervention
Patient Noncompliance	Customized Adherence Enhancement (CAE)	Subjects enrolled in the study will receive both Abilify Miantena and the Customized Adherence Enhancement (CAE) intervention

Primary Outcome Measures

Name	Time	Method
Change in Tablets Routine Questionnaire (TRQ, Past Week)	Screen to Week 24	Treatment non-adherence is measured as a percentage of medications not taken within the past week at time of assessment. The minimum score is 0% and the maximum score is 100%. A higher score implies poorer treatment adherence.
LAI Injection Adherence	Baseline to Week 24	LAI injection adherence will be determined as a proportion of LAI injections received at the appropriate time (within 7 days of scheduled time).
Change in Tablets Routine Questionnaire (TRQ, Past Month)	Screen to Week 24	Treatment non-adherence is measured as a percentage of medications not taken within the past month at time of assessment. The minimum score is 0 and the maximum score is 100. A higher score implies poorer treatment adherence.

Secondary Outcome Measures

Name	Time	Method
Change in the Brief Psychiatric Rating Scale (BPRS) Score	Baseline to Week 24	The BPRS measure psychiatric symptoms such as depression, anxiety, hallucinations and unusual behavior. The minimum score is 18 and the maximum score is 126. A higher score implies a worse condition.
Change in Clinical Global Impressions (CGI) Score	Screen to Week 24	The minimum possible score is 1 and the maximum score is 7. A higher score implies a worse condition.
Change in Social and Occupational Functioning Assessment Scale (SOFAS) Score	Baseline to Week 24	The SOFAS measures social and occupational functioning independent of the overall severity of the individual's psychological symptoms. The minimum score is 0 and the maximum score is 100. A higher rating implies a higher level of functioning.
Change in The Self-Report Habit Index (SRHI) Score	Screen to Week 24	The SRHI is a measure of habit strength. The minimum score is 12 and the maximum score is 84. A higher score implies stronger habits.
Change in Young Mania Rating Scale (YMRS) Score	Screen to Week 24	The YMRS measures symptoms of mania. The minimum possible score is 0 and the maximum score is 60. A higher score implies a worse condition.
Change in Montgomery Asberg Rating Scale (MADRS) Score	Screen to Week 24	The MADRS measures symptoms of depression. The minimum possible score is 0 and the maximum score is 60. A higher score implies a worse condition.
Change in Drug Attitude Inventory (DAI) Score	Screen to Week 24	DAI-10 scoring ranges from -10 to +10 with a total score \>0 indicating a positive attitude toward psychiatric medications and a total score of \<0 indicating a negative attitude toward psychiatric medications
Change in Attitude Towards Medication Questionnaire (AMSQ) Score	Screen to Week 24	A modification of the Lithium Attitudes Questionnaire (Harvey 1991) which evaluates an individual's attitudes towards mood stabilizers. The AMSQ is used to measure attitudes towards medications. The scale contains 19 items grouped into 7 subscales: general opposition to prophylaxis (4 items), denial of therapeutic effectiveness (2 items), fear of side effects (2 items), difficulty with medication routines (4 items), denial of illness severity (3 items), negative attitudes toward drugs in general (3 items), and lack of information about psychiatric medication (1 item). Responses which suggest positive attitudes towards medications are scored "0", while responses which suggest negative attitudes towards medications are scored "1". The items scores are added for a total score which is reported, with the minimum total score of 0 and maximum total score of 19. Higher scores on each subscale represent more negative attitudes toward mood stabilizers.
Change in Global Assessment of Functioning (GAF) Score	Baseline to Week 24	The minimum score is 1 and the maximum score is 100. A higher score implies higher functioning.
Change in Oxford Bipolar Knowledge Questionnaires (OBQ) Score	Screen to Week 24	The OBQ assess knowledge of BD management. Total score rangers from 0-80, with a higher score indicative of better knowledge of bipolar mood management.
Change in Communication Styles Scale Score	Screen to Week 24	The Communication Styles Scale is a measure of the impact of physician communication style on medication beliefs and adherence behavior. Total scores range from 0-27 where the higher score indicates a more initial collaborative communication style.
Change in Stages of Change Readiness and Treatment Eagerness Scale (SOCRATES 8A) Score	Screen to Week 24	The SOCRATES measures motivation to reduce the use of substances. The minimum score is 10 and the maximum score is 50. A higher score indicates a higher desire to reduce drinking.