Hemiparesis, Stroke
Conditions
Keywords
Stroke, Upper member, Neurorehabilitation, Mirror therapy, Therapeutic cognitive exercise, Perfetti
Brief summary
This is a randomized clinical trial aimed at patients with a diagnosis of residual hemiparesis due to ischemic or hemorrhagic stroke. Its objective is to evaluate the effects of the mirror therapy and cognitive therapeutic exercise, both in combination with task-oriented motor learning, to achieve maximum functionality of the affected upper member,
Detailed description
Objective: To assess the effect at 3 months of the of the mirror therapy and cognitive therapeutic exercise, both in combination with task-oriented motor learning, applied for 30 days in the functionality of the affected upper member, cognitive performance, emotional state, performance of daily living activities and quality of life in stroke patients. Design and setting: A randomized clinical trial of three parallel groups. Population: 152 patients with residual hemiparesis due to ischemic or hemorrhagic stroke will be included, selected by consecutive sampling at the Neurological Service and Stroke Unit of the University Hospital of Burgos (HUBU). Measurements and intervention: Functionality of the affected upper member, cognitive performance, emotional state, performance of daily living activities and health-related quality of life will be evaluated. The intervention groups will receive a treatment based either on mirror therapy or on congnitive therapeutic exercise, both combined with task-oriented motor learning for 30 days. No additional intervention with the participants of the control group will be completed.
Interventions
BEHAVIORALMirror therapy
The intervention will take place at the home of the participant for 6 weeks (30 days), during 60-minute sessions, 30 of which will be for mirror therapy, while the remaining 30 minutes will be for task-oriented motor learning
BEHAVIORALCognitive therapeutic exercise
The intervention will take place at the home of the participant for 6 weeks (30 days), during 60-minute sessions, 30 of which will be for cognoscitive therapeutic exercise, while the remaining 30 minutes will be for task-oriented motor learning
Sponsors
Castilla-León Health Service
Universidad de Burgos
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* Diagnosis of residual hemiparesis due to ischemic or hemorrhagic stroke, * Movements of the affected upper members classified between stages II and IV on the Brunnstrom Scale * Score on the Montreal Cognitive Assessment (MOCA) scale equal to or over 26
Exclusion criteria
* Heminegligence * Wernicke's aphasia * Visual deficits (homonymous hemianopsia)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Functionality of the affected upper member. | 3 months | Measurement by Fugl-Meyer Scale: Score between 0 (worst functionality) and 126 (best functionality) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Spasticity of the upper member | 3 months | Measurement by Ashworth Scale: Score between 0 (best situation) and 5 (worst situation) |
| Cognitive performance. | 3 months | Measurement by Montreal Cognitive Assessment Scale: Score between 0 (worst cognitive situation ) and 30 (best cognitive situation) |
| Emotional state and quality of life. | 3 months | Measurement by Post-Stroke Quality of Life Scale: Score between 30 (best state) and 155 (worst state) |
| Basic Daily Living Activities | 3 months | Measurement by Functional Independence Measure - Functional Assessment Measure: Score between 30 (worst situation) and 210 (best situation) |
| Instrumental activities of daily living | 3 months | Measurement by Lawton-Brody Index: Score between 0 (worst state) and 6 (best state) |
Countries
Spain
Contacts
Primary ContactRaul Soto-Camara, PhD
Backup ContactJeronimo Gonzalez-Bernal, PhD
Outcome results
None listed