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Neuropsychiatric symptoms related to COVID-19: follow-up study

Characterization of Neuropsychiatric, Neuropsychological, Radiological and Biological Findings on the Investigation of the impact of COVID-19 on Central Nervous System: a Cohort Study - NEUROPSYCHOVID NEUROlogical, PSYCHiatric and NEUROPSYCHological Manifestations of COVID-19

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-8z7v5wc
Enrollment
Unknown
Registered
2021-02-05
Start date
2020-10-20
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

New Coronavirus Disease 2019 (COVID-19)

Interventions

Structured evaluations to ascertain mental state, cognition and neurological signs
correlations with COVID-related clinical symptoms and biological markers. The assessment protocol will be applied to all participants (cases and controls). In brief, the interventions will comprise: 1
post-traumatic stress disorder ()PCL-C)
psychosis (SCID-5-RV)
alcohol use disorders (AUDIT) e suicide risk (ASQ). 2) Neurological examination: (a) Brief cognitive assessment: level of arousal and consciousness
temporal orientation
language. (b) Somatic examination: pronator drift test
speed of movement, upper limbs (finger tap, forearm rolling test)
extensor plantar skin reflex/Babinnski sign
cerebelar ataxia (index-nose test and gait)
sensitivity (only in patients with abnormal response in thermal/pain sensitivity test on four limbs). (c) cranial nerves: ocular and facial motricity
gaze-evoked nistagmus. (d) meningeal signs: nuchal rigidity, Brudzinski sign. 3) Neuropsichological examination: verbal IQ according to vocabulary and similarities (as an estimate of pre-morbid IQ). N
9615
54753

Sponsors

Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP)
Lead Sponsor
Laboratórios de Investigação Médica (LIMs) - HCFMUSP
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Previous history of COVID-19 leading to significant medical morbidity/hospital admission and willingness/consent to perform follow-up interviews and examinations starting 6 months after remission of index episode/hospital discharge

Exclusion criteria

Exclusion criteria: Unavailability or refusal to perform multidisciplinary evaluations

Design outcomes

Primary

MeasureTime frame
Primary outcome: incidence of psychiatric symptoms in the long-term outcome post-COVID19; method to ascertain outcome: psychiatric assessment protocol comprising the Clinical Interview Schedule - Revised (CIS-R), Structured Clinical Interview for DSM-5 Disorders, Revised (SCID-5-RV), Hospital Anxiety and Depression Scale (HADS), Post-Traumatic Stress Disorder Checklist (PCL-C), Ask Suicide-Screening Questions (ASQ), Alcohol Use Disorder Identification Test (AUDIT); criterion: classification of 'positive' and 'negative' cases according to the output of structured interviews (CIS-R and SCID_VR) and cut-off scores defined for the instruments. Secondary outcomes: incidence of memory complaints and neuropsychological symptoms in the long-term outcome post-COVID19; method to ascertain outcome: cognitive assessment battery comprising: Memory Complaint Scale (MCS), Mini-Mental State Examination (MMSE ), Memory Sub-scale of the Consortium to Establish a Diagnostic Registry for Alzheimer's Disease (CERAD), Trail-Making Test Version A (TMT-A), Verbal Fluency Test (VFT); criterion: classification of 'positive' and 'negative' cases according to cut-off scores defined for the instruments.

Countries

Brazil

Contacts

Public ContactRodolfo Damiano
damianorf@gmail.com+55-11-998100333

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 15, 2026