Ignite Creation Date:
2026-03-26 @ 3:20 PM
Ignite Modification Date:
2026-03-31 @ 11:48 AM
Study NCT ID:
NCT07453420
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2026-03-06
First Post:
2026-03-01
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Profiling Vulnerability and Resilience for Mental Illness Following Viral Infections: Translating Epidemiology to Deep-phenotyping.
Sponsor:
Shalvata Mental Health Center
Organization:
Study Overview
Official Title:
Profiling Vulnerability and Resilience for Mental Illness Following Viral Infections: Translating Epidemiology to Deep-phenotyping.
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2026-03
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
Viral-MI
Brief Summary:
The study protocol was submitted to ERA-NET NEURON for funding on 28/06/2023. Description of the Israeli responsibilities was extracted from the full submitted research protocol. The protocol includes two studies (CHS1 and CHS2). At the time of the study registration CHS1 was partially analyzed whereas CHS2 has not been initiated. See below the full description of the two studies' protocols.
To explore the probability of mental illness (MI) onset or psychiatric relapse following infections, we will utilize two databases from the CHS registries from Israel (n=50,000, n=69,594). Participants with a high load of past infections (cohort 1, n=50,000) will be identified and matched in a 1:1 ratio to controls by age and sex. Probability of MI onset across a broad range of psychiatric disorders, including depression, bipolar disorder, anxiety and psychotic disorders will be explored. The probability of psychiatric relapse among individuals with pre-existing mental disorder following infection will be investigated in a cohort of 34,797 individuals with schizophrenia matched randomly to age and sex controls with no diagnosis of schizophrenia (n = 34,797) (cohort 2, total n=69,594, 5). Socio and sociodemographic factors which might serve as vulnerability or resilience factors will be assessed across both cohorts, and will include environmental factors such as socioeconomic status, familial status, healthcare utilization information and demographic factors.
In addition, The CHS databases (n=50,000, n=69,594) will be utilized to study outcomes of infections in SMI. From the CHS databases in Israel, outcome of infections will be assessed in the two previously described cohorts. Severe outcomes will be defined as hospital admission \~two weeks after a diagnosis of an infection, among individuals with pre-existing anxiety, depression, bipolar diagnosis (n=50,000), and among patients with schizophrenia (n=69,594), as well as all-cause mortality. The following infections will be considered: Epstein Barr Virus, Cytomegalovirus, Toxoplasma Gondii, COVID-19, and Herpes viruses. Environmental protective and risk factors and their moderating role in the association between infection and outcome will include marital status, number of siblings, and sociodemographic factors. Vulnerability factors such as smoking, obesity, and comorbid physical illness will also be examined.
The presence of pre-existing viral infections will be assessed as a potential vulnerability factor.
To explore the probability of mental illness (MI) onset or psychiatric relapse following infections, we will utilize two databases from the CHS registries from Israel (n=50,000, n=69,594). Participants with a high load of past infections (cohort 1, n=50,000) will be identified and matched in a 1:1 ratio to controls by age and sex. Probability of MI onset across a broad range of psychiatric disorders, including depression, bipolar disorder, anxiety and psychotic disorders will be explored. The probability of psychiatric relapse among individuals with pre-existing mental disorder following infection will be investigated in a cohort of 34,797 individuals with schizophrenia matched randomly to age and sex controls with no diagnosis of schizophrenia (n = 34,797) (cohort 2, total n=69,594, 5). Socio and sociodemographic factors which might serve as vulnerability or resilience factors will be assessed across both cohorts, and will include environmental factors such as socioeconomic status, familial status, healthcare utilization information and demographic factors.
In addition, The CHS databases (n=50,000, n=69,594) will be utilized to study outcomes of infections in SMI. From the CHS databases in Israel, outcome of infections will be assessed in the two previously described cohorts. Severe outcomes will be defined as hospital admission \~two weeks after a diagnosis of an infection, among individuals with pre-existing anxiety, depression, bipolar diagnosis (n=50,000), and among patients with schizophrenia (n=69,594), as well as all-cause mortality. The following infections will be considered: Epstein Barr Virus, Cytomegalovirus, Toxoplasma Gondii, COVID-19, and Herpes viruses. Environmental protective and risk factors and their moderating role in the association between infection and outcome will include marital status, number of siblings, and sociodemographic factors. Vulnerability factors such as smoking, obesity, and comorbid physical illness will also be examined.
The presence of pre-existing viral infections will be assessed as a potential vulnerability factor.
Detailed Description:
The Israel cohort consists of two databases from the Clalit Health Services (CHS) registries from Israel (CHS1 n=50,000, CHS2 n=69,594). The CHS is the largest of four operating healthcare organisations to provide healthcare to all citizens of Israel, and covers more than 50% of Israel's population. The CHS databases undergo periodic updating processes and have been validated by the registry algorithm as well as by many scientific organisations utilising the database. The diagnoses of chronic diseases are based on real-time input from healthcare providers, pharmacies, medical care facilities, and administrative computerised operating systems. Psychiatric Diagnoses are based on the ICD-9 and ICD-10 classifications. To evaluate probability of MI following infection and post-infection outcomes(CHS1), individuals with a high load of past infections will be identified and matched in a 1:1 ratio to controls by age and sex. Probability of MI onset across a broad range of psychiatric disorders will be explored among the high load and control groups, including depression, BD, anxiety and psychotic disorders. Inclusion criteria: individuals insured by the CHS since birth and with at least 10 years of follow up; exclusion criteria include termination of insurance and lack of successive medical follow up. To evaluate the probability of psychiatric relapse among individuals with pre-existing mental disorder following infection (CHS2), a cohort of 34,797 individuals with schizophrenia matched randomly to age and sex HC with no diagnosis of schizophrenia will be exploited. Inclusion criteria for this sample is an active diagnosis of schizophrenia in CHS registries during stages of analyses, and place of residence is at the CHS hospital catchment areas (to ensure psychiatric hospitalisation is fully registered); exclusion criteria include lack of active diagnosis and place of residency outside of CHS catchment area. Across both cohorts, socioeconomic status, familial status, marital status, number of siblings, smoking, obesity, diabetes, hypertension, hyperlipidemia, chronic obstructive pulmonary disease and ischemic heart disease, as well as healthcare utilisation and other demographic variables have been collected. The following infections will be considered across both cohorts: Epstein Barr Virus, Cytomegalovirus, Toxoplasma Gondii, COVID-19, and Herpes viruses. Measures of inflammation include neutrophil/lymphocyte ratio and systemic inflammatory index.
To demonstrate an association between infections, with a particular focus on viral ones, severe MI and post-infection severe outcomes (Objective 1), we will compute hazard ratios (HRs) to assess the risk of SMI development or psychiatric relapse following infection using Cox proportional hazard regression models in all three cohorts (CHS1, CHS2). Incidence rates and crude and adjusted models controlling for demographic and clinical factors will be reported. The proportional hazard assumption will be tested as the correlation between the Schoenfeld residuals and survival time, with significance level of p\<0.05 indicating non-proportionality. Estimated projections of the cumulative probability of severe outcome among individuals with pre-existing SMI will be obtained by Kaplan-Meier analysis. Confounding, moderation and mediation patterns of environmental (socio and sociodemographic) and biological (inflammatory, polygenic risk score (PRS) for MI and immune-related conditions) mechanisms will be assessed using the PROCESS macro, a simulation-based strategy based on re-sampling (bootstrapping) techniques. Direct and indirect effects, standard errors and confidence intervals will be estimated based on the bootstrap distribution found with 10,000 bias-corrected resamples. PRS will be computed following the method described by Purcell et al. Analyses will be performed based on the directed acyclic graph (DAG) causal framework, ensuring transparent model assumptions and minimising bias. All three databases provide nation-wide representative data and have proven their efficiency in characterising MI cohorts and associations with environmental factors, as shown by high impact publications .
To demonstrate an association between infections, with a particular focus on viral ones, severe MI and post-infection severe outcomes (Objective 1), we will compute hazard ratios (HRs) to assess the risk of SMI development or psychiatric relapse following infection using Cox proportional hazard regression models in all three cohorts (CHS1, CHS2). Incidence rates and crude and adjusted models controlling for demographic and clinical factors will be reported. The proportional hazard assumption will be tested as the correlation between the Schoenfeld residuals and survival time, with significance level of p\<0.05 indicating non-proportionality. Estimated projections of the cumulative probability of severe outcome among individuals with pre-existing SMI will be obtained by Kaplan-Meier analysis. Confounding, moderation and mediation patterns of environmental (socio and sociodemographic) and biological (inflammatory, polygenic risk score (PRS) for MI and immune-related conditions) mechanisms will be assessed using the PROCESS macro, a simulation-based strategy based on re-sampling (bootstrapping) techniques. Direct and indirect effects, standard errors and confidence intervals will be estimated based on the bootstrap distribution found with 10,000 bias-corrected resamples. PRS will be computed following the method described by Purcell et al. Analyses will be performed based on the directed acyclic graph (DAG) causal framework, ensuring transparent model assumptions and minimising bias. All three databases provide nation-wide representative data and have proven their efficiency in characterising MI cohorts and associations with environmental factors, as shown by high impact publications .
Study Oversight
Has Oversight DMC:
False
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
Secondary ID Infos
| Secondary ID | Type | Domain | Link | View |
|---|---|---|---|---|
| NEURON_RV-086 | OTHER_GRANT | NEURON, the 'Network of European Funding for Neuroscience Research' established under the ERA-NET | View |