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Effect of cognitive stimulation in patients with stroke

Effect of cognitive stimulation on the attentional performance of patients diagnosed with stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-10935tq4
Enrollment
Unknown
Registered
2021-02-08
Start date
2020-11-09
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

Stroke, Attention, Cognitive Impairment, Depression

Interventions

The intervention will be performed in a single group (there will be no control group) with 15 patients. During these three months weekly meetings will be held with 90 minutes each. The intervention w

Sponsors

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

Eligibility

Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: The present study will be carried out with individuals of both sexes, aged over 40 years, who suffered a stroke for a maximum of one year.

Exclusion criteria

Exclusion criteria: Illiterate individuals and/or individuals who have significant impairment and who prevent them from carrying out cognitive and mood assessment activities.

Design outcomes

Primary

MeasureTime frame
Improve the participants' cognitive performance, especially related to attention, 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
Improve the participants' depressive symptoms as measured by the result of the BDI-II test applied over a period of at most two months before and after the intervention. 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
nadia.shigaeff@ufjf.edu.br+553221023117

Outcome results

None listed

Source: REBEC (via WHO ICTRP)