Sustainable Early Episode Clinic Study (SEEC) (NCT03571685) | Clinical Trial Compass
CompletedNot Applicable
Sustainable Early Episode Clinic Study (SEEC)
United States50 participantsStarted 2017-01-31
Plain-language summary
The purpose of this study is to describe relapse rates among participants receiving services in the SEEC program high intensity resource use. For purposes of this study, relapse will be defined as: Psychiatric hospitalization; Psychiatric emergency department visits; Ambulatory acute services (Partial Hospitalization Program, Intensive Outpatient Program, Crisis House stay).
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria - Participants
* Participants must be at least 18 years or older
* Participants within 5 years of a clinical diagnosis of Schizophrenia or Schizoaffective disorder made by a clinician with understanding of the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for these disorders
* Participants must be able to speak, read, and understand English
* Participants must sign an informed consent form
Inclusion Criteria - Caregivers
* Caregivers must be 18 years or older Caregivers must also be willing to attend the multi-family psychoeducation group series (Phase I)
* Caregivers must be willing to participate in monthly family therapy and/or monthly phone contact with staff for the duration of the study
* Caregivers must sign informed consent form
Exclusion Criteria - Participants
* Co-occurring developmental disabilities
* Receiving electroconvulsive therapy
* Primary substance use disorder
* On permanent conservatorship
* Unable to complete baseline assessments due to acuity of psychiatric symptoms
Exclusion Criteria - Caregivers
* Caregivers who refuse to participate in the psychoeducation series of Phase 1
* Caregivers who refuse monthly family therapy/phone contact with staff will be excluded
* Caregiver is mentally or physically incapable of adequately performing the required study procedures, as determined by treatment team
* Caregiver is an employee of the investigator or study site, with direct involvement in the…