stroke
Conditions
Interventions
This is a controlled randomized clinical study, single-blinded. A total of 30 eligible individuals will be probabilistically allocated to either intervention group using a random number table, which w
E02.760.169.063.500
Sponsors
Instituto de Ensino e Pesquisa Alberto Santos Dumont
Instituto de Ensino e Pesquisa Alberto Santos Dumont
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Individuals with hemiparesis post-stroke; over 18 years old; of both sexes; in the chronic phase; capable of performing residual movement in the paretic limb with assistance or device; who do not present contractures or deformities in upper limbs; with a score of 2 on the Modified Ashworth Scale and with a score on the Mini-Mental State Examination
Exclusion criteria
Exclusion criteria: Participants presenting neglect syndrome; significant pain in the limb, excessive fatigue, non-preserved cognition, inability to perform or understand the necessary procedures; and those who do not follow the protocol during the established period will be excluded from the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in motor control, assessed by the Fugl-Meyer scale. Data will be collected one week before the intervention and one week after the intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in activities of daily living, assessed by the Motor Activity Log scale, with one point of improvement considered clinically significant. Data will be collected one week before the intervention and one week after the intervention | — |
Countries
Brazil
Contacts
Public ContactFabrício Brasil
Instituto de Ensino e Pesquisa Alberto Santos Dumont
Outcome results
None listed