Age
Item
1. men and women, ages 18 to 60 years, inclusive. earliest inclusion day is the 18th birthday and the latest is the day before the 61st birthday.
boolean
C0001779 (UMLS CUI [1])
Schizophrenia | Schizoaffective Disorder
Item
2. a diagnosis of schizophrenia or schizoaffective disorder according to icd-10 classification.
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
At risk for relapse | Hospitalization Quantity Psychotic Disorders
Item
3. increased risk for relapse, defined as having at least 1 psychiatric hospitalization for psychosis within the past 3 years and at least 2 psychiatric hospitalizations for psychosis in total (i.e. ≥ 2 hospitalizations).
boolean
C1320679 (UMLS CUI [1])
C0019993 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0033975 (UMLS CUI [2,3])
Clinical global impression scale
Item
4. clinical global impression scale - severity (cgi-s) ≤ 3 at study visit 1.
boolean
C3639708 (UMLS CUI [1])
Antipsychotic Agents Dose Stable
Item
5. all patients must be on stable doses of antipsychotic medication during the study entry.
boolean
C0040615 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Organic mental disorder Absent | Absence Mental disorder Due to Psychoactive substance | Absence Mental disorder Due to Mental Retardation
Item
6. absence of organic mental disorder, mental disorder due to psychoactive substance use or mental retardation.
boolean
C0029227 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0332197 (UMLS CUI [2,1])
C0004936 (UMLS CUI [2,2])
C0678226 (UMLS CUI [2,3])
C0682880 (UMLS CUI [2,4])
C0332197 (UMLS CUI [3,1])
C0004936 (UMLS CUI [3,2])
C0678226 (UMLS CUI [3,3])
C0025362 (UMLS CUI [3,4])
Presence Family member cooperative | Presence Caregiver
Item
7. presence of a cooperating family member, caregiver or other person who is in frequent contact with the patient (at least 4 times a week) and who is willing to participate in the trial.
boolean
C0150312 (UMLS CUI [1,1])
C0086282 (UMLS CUI [1,2])
C0679729 (UMLS CUI [1,3])
C0150312 (UMLS CUI [2,1])
C0085537 (UMLS CUI [2,2])
Informed Consent
Item
8. signed written informed consent. the informed consent process must be documented by signing the informed consent form prior to any study-related procedures.
boolean
C0021430 (UMLS CUI [1])
Mobile Phone Communication
Item
9. eligibility for mobile phone communicating.
boolean
C1136360 (UMLS CUI [1,1])
C0009452 (UMLS CUI [1,2])
Study Subject Participation Status | Relapse Prevention | Interventional procedure
Item
1. participation in another relapse prevention program or another interventional clinical trial will be prohibited during the entire participation in the study. subjects enrolled in observational (non-interventional) trials are not excluded from this study.
boolean
C2348568 (UMLS CUI [1])
C0679867 (UMLS CUI [2])
C0184661 (UMLS CUI [3])
Compliance behavior Rating scale
Item
2. hayward compliance rating scale score < 2 at visit 1.
boolean
C1321605 (UMLS CUI [1,1])
C0681889 (UMLS CUI [1,2])