Family Intervention in Recent Onset Schizophrenia Treatment (FIRST)
NCT02600741 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 296
Last updated 2019-01-23
Summary
The primary purpose of this study is to evaluate the overall effect of caregivers receiving a study-provided caregiver psycho-education and skills training program on the number of treatment failures (psychiatric hospitalization, psychiatric emergency room (ER) visit, crisis center visit, mobile crisis unit intervention, arrest/incarceration, and suicide or suicide attempt) in patients under their care during a 12 month period.
Conditions
Interventions
- OTHER
-
Caregiver psycho-education and skills training
Caregivers will receive up to 16 sessions of study-provided caregiver psycho-education and skills training sessions they are able to attend within a 6-month period.
- OTHER
-
Caregiver support available at the study site
Caregivers will receive whatever caregiver support that is customarily available at the study site, if any.
- DRUG
-
Paliperidone palmitate
Patients enrolled in this study will continue to receive routine treatment of paliperidone palmitate, as directed by their treating physician.
- DRUG
-
Chlorpromazine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Droperidol
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Fluphenazine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Haloperidol
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Loxapine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Perphenazine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Pimozide
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Prochlorperazine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Thiothixene
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Thioridazine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Trifluoperazine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Aripiprazole
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Asenapine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Paliperidone
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Quetiapine
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Risperidone
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
- DRUG
-
Ziprasidone
Patients enrolled in this study will continue to receive routine treatment of oral antipsychotics, as directed by their treating physician.
Sponsors & Collaborators
-
Janssen Scientific Affairs, LLC
lead INDUSTRY
Principal Investigators
-
Janssen Scientific Affairs, LLC Clinical Trial · Janssen Scientific Affairs, LLC
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-07-24
- Primary Completion
- 2018-07-05
- Completion
- 2018-07-05
Countries
- United States
Study Locations
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