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Assessment of the effectiveness of cognitive rehabilitation as a therapeutic strategy for patients diagnosed with COVID19 and cognitive symptoms

Clinical trial on the effect of cognitive rehabilitation in individuals with COVID-19

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-967k5py
Enrollment
Unknown
Registered
2022-08-09
Start date
2021-06-01
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

Cognitive Dysfunction

Interventions

The intervention will be carried out in the experimental group. The selection of participants for the experimental group or the control group will be performed randomly. Each group will have a total o

Sponsors

Universidade Federal de Juiz de Fora
Lead Sponsor
Universidade Federal de Juiz de Fora
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Participants residing in Juiz de Fora (MG) with a confirmed diagnosis of COVID-19 by PCR within a period of up to six months before inclusion in the study; over 18 years of age; and literate (enough to guarantee the reading of words or phrases in the execution of the cognitive tests).

Exclusion criteria

Exclusion criteria: Participants who present a neurological and/or psychiatric diagnosis that justify previous impairments or that make it impossible to adhere to and understand the cognitive assessment tasks.

Design outcomes

Primary

MeasureTime frame
Expressive and faster improvement in cognitive performance of participants who participate in the cognitive rehabilitation program, assessed through the results of neuropsychological assessment tests. Data collected in a period of at most two months before and after the intervention by cognitive training. From the inferential statistical analysis, of comparison of means, the comparison will be performed by means of analysis of variance (ANOVA) and also via non-parametric test of minimal detectable changes.

Secondary

MeasureTime frame
Decrease in depressive symptoms and impairment of functionality of participants who participate in the cognitive rehabilitation program, assessed through the results of neuropsychological assessment tests. Data collected in a period of at most two months before and after the intervention by cognitive training. From the inferential statistical analysis, of comparison of means, the comparison will be performed by means of analysis of variance (ANOVA) and also via non-parametric test of minimal detectable changes.

Countries

Brazil

Contacts

Public ContactNadia Shigaeff

Universidade Federal de Juiz de Fora

nadia.shigaeff@ufjf.br+553221023117

Outcome results

None listed

Source: REBEC (via WHO ICTRP)