Improving the Quality of Life of Stroke Patients Using the Armeo Spring Device

NCT05743413 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2023-06-22

No results posted yet for this study

Summary

The main goal will be to evaluate the effect of improving the quality of movement of the upper limb (using an evaluation exercise in the software of the Armeo Spring device) on the development of the quality of life after stroke using a standardized generic and specific questionnaire.

The secondary outcome will be to evaluate changes in self-sufficiency using a test of daily activities modified by the Frenchay test of daily activities.

Conditions

Interventions

PROCEDURE

Armeo Spring physiotherapy

Study subjects will undergo physiotherapy sessions using the Armeo Spring device.

PROCEDURE

Standard physiotherapy

Study subjects will undergo standard physiotherapy sessions.

Sponsors & Collaborators

  • University of Ostrava

    collaborator OTHER
  • University Hospital Ostrava

    lead OTHER

Principal Investigators

  • Šárka Anežka Čechová, MD · University Hospital Ostrava

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-01
Primary Completion
2023-08-31
Completion
2023-10-31

Countries

  • Czechia

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05743413 on ClinicalTrials.gov