Paresis
Conditions
Interventions
Experimental group: 15 participants will receive CIMT (Constraint-Induced Movement Therapy) with a treatment protocol consisting of 2 weeks, 5 weekly sessions lasting 3 hours of activities with the pa
Device
Behavioural
E07.101.036
F04.754.137
Sponsors
Universidade Federal de Ciências da Saúde de Porto Alegre
Universidade Federal de Ciências da Saúde de Porto Alegre
Eligibility
Age
5 Years to 60 Years
Inclusion criteria
Inclusion criteria: Hemiparetic individuals in upper limb; both genders; 5 to 60 years; Signature of the Informed Consent Form (TCLE); diagnosis of neurological injury; minimum motor criterion for the execution of the TCI; without cognitive deficit.
Exclusion criteria
Exclusion criteria: Allergy to Functional Bandage
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: 5 ° increase in joint range of motion, measured by goniometer before and after intervention;Expected outcome 2: Reduction of the degree of spasticity, measured through the Modified Ashworth Scale before and after intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 1: Reduction of the execution time of the specific tasks, as measured by the Wolf Motor Function Test (WMFT), before and after intervention;Expected outcome 2: Increase in the quality and quantity of specific movements, as measured by Motor Activity Log (MAL) before and after intervention | — |
Countries
Brazil
Contacts
Public ContactFernanda Cechetti
Universidade Federal de Ciências da Saúde de Porto Alegre
Outcome results
None listed