The effect of Reac treatment compared to placebo on the balance of individuals affected by stroke

Phase 4

Recruiting

• Conditions: Paresis; C10.228.140.300.775

• Registration Number: RBR-33sd66h
• Lead Sponsor: Asmed Latino America Comércio e Importação de Produtos Médicos Ltda

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2024-01-11
• Last Update Posted: 23 January 2024
• Study Completion: 2025-06-20

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Diagnosis of right or left hemispheric stroke of ischemic or hemorrhagic origin. Physiotherapeutic diagnosis of right or left hemiparesis due to stroke. Chronic cerebrovascular injury (injury time greater than 6 months). Absence of obvious orthopedic or neurological disorders not resulting from the stroke that could interfere with balance. Absence of rheumatic disorders with joint involvement of the lower limbs.
Have not participated in other clinical trials related to the use of transcranial stimulation within one month. Use of medications that may interfere with the assessment of study efficacy, such as opioids, barbiturates, benzodiazepines and antipsychotics. Ability to understand and execute simple verbal commands. Ability to remain upright for at least 60 seconds without the need for human support or an assistive device. Ability to walk without human assistance, being allowed to use an auxiliary device

Exclusion Criteria

Failing to complete assessments of outcome measures before and after REAC treatment with NPO (neurpostural optimization) protocol. Instability of vital signs at the time of study procedures. Report of dizziness at the time of the data collection procedure

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
It is expected to find an increase in the score of Berg Balance Scale Score

Secondary Outcome Measures

Name	Time	Method
It is expected that the time to perform the Time Up and Go Test will be shorter after applying the intervention;a reduction in functional dysmetria is expected;A smaller asymmetry of the center of pressure area is expected;A reduction in asymmetry in weight bearing is expected;Better synchronization of the center of pressure is expected