Research and Evaluation of Antipsychotic Treatment in Community Behavioral Health Organizations

This is a prospective observational study of usual care of patients undergoing treatment for
schizophrenia or bipolar I disorder at CBHOs. Up to 50 CBHOs will be selected as sites for
this study. Treating clinicians at these sites will notify the designated research
coordinators for this study when they are initiating a patient on a new antipsychotic
medication (including risperidone long acting injectable or paliperidone palmitate) or if
they are treating a patient with risperidone long acting injectable or paliperidone
palmitate. New initiation will include patients not previously on any antipsychotic
medication as well as those switched from one antipsychotic to another. Switches may
include but are not limited to switches among different types of oral antipsychotics, from
an oral antipsychotic to Long Acting Therapy (LAT), or from LAT to an oral antipsychotic.
Site research staff will screen potential participants identified by the clinicians and
enroll those meeting study criteria who consent to study participation. Sites will maintain
a screening log of all potential participants. The target enrollment for this study is up to
2,450 participants. Enrollment by cohort will be monitored and sites will be notified to
stop enrollment if target enrollment for a particular cohort has been reached. Eligible
participants who consent to the study will be recruited into one of two samples:
participants with a schizophrenia diagnosis (target n=2,250) and participants with a bipolar
I disorder diagnosis (target n=200). There will be four cohorts: risperidone long acting
injectable new starts (target n=475); risperidone long acting injectable continuous users
(target n=75); paliperidone palmitate new starts or continuous users (target n=1,200); and
other antipsychotic new starts (target n=700). During the entire study follow-up period
participants will receive their medication per usual care in their treatment setting and no
study drug will be provided. Enrolled participants will be followed prospectively over a
12-month study period, with interviews at baseline, 6 and 12 months. Sites will also
abstract medical history and healthcare utilization information from the chart of each
enrolled participant. There will be three chart abstractions (baseline, 6 Months, 12
Months). The baseline abstraction will cover services rendered in the 6 months prior to
antipsychotic initiation or switch, or from their first visit to the CBHO if the individual
did not receive services for as long as 6 months prior to initiation or switch. The 6M and
12M abstractions will each cover services rendered in the prior 6 months. When all three
abstractions are complete, the data will cover the period from 6 months before baseline to
12 months after baseline. If a Serious Adverse Event (SAE) associated with a J&J medicinal
product occurs the investigator will record it in the source document as well as fax the SAE
form to J&J internal safety group within 24 hours. Treatment as usual

Inclusion Criteria:

- Diagnosed with schizophrenia or bipolar I disorder

- Antipsychotic use in one of the following categories: Clinician ordered initiation of
Risperidone long acting injectable in the 4 weeks prior to or on the day of
enrollment (includes patients not previously on any antipsychotic medication and
those switched from another antipsychotic)

- On continuous Risperidone long acting injectable for at least 6 months prior to
enrollment (no gaps between injections>30 days)

- Clinician ordered initiation of Paliperidone Palmitate in the 4 weeks prior to or on
the day of enrollment (includes patients not previously on any antipsychotic
medication and those switched from another antipsychotic)

- or on continuous Paliperidone Palmitate for any time period prior to enrollment

- Clinician ordered initiation of another antipsychotic in the 4 weeks prior to or on
the day of enrollment (includes patients not previously on any antipsychotic
medication and those switched from another antipsychotic)

- Not enrolled in another clinical study

- Primary source of care for schizophrenia or bipolar I disorder is the recruiting CBHO

- Agrees to all study procedures/interviews

- must sign the study informed consent document indicating that they understand the
purpose of and procedures required for the study and are willing to participate in
the study

Exclusion Criteria:

- Currently participating in a clinical study (e.g. clinical trial or observational
study) or participated in a clinical study within the past 30 days