Informative of Surface Electromyography and Prognostic Factors in Assessing the Recovery of Balance and Gait After Stroke
NCT ID: NCT04981184
Last Updated: 2024-10-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
100 participants
INTERVENTIONAL
2019-07-22
2026-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effectiveness of a Neuromuscular Exercise Program and Visual Feedback in the Management of Body Position for Stroke Survivors
NCT05187559
A Novel, Comprehensive Approach to Post-stroke Gait Rehabilitation
NCT04411303
Longitudinal Multimodal Profiling of Balance and Gait In Stroke
NCT06187467
Comparison of the Effects of Ordinary and Differential Learning Based Physiotherapy on Subjects With Ischemic Stroke Torso Control, Balance and Gait in the Second Phase of Rehabilitation
NCT04985162
Assessment of Robotic Assistance on Gait Parameters Among Healthy Subjects and Brain Damaged Patients
NCT05264103
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Gait and balance measurement
Gait analysis with surface electromyography measurement: surface electromyography signals (of affected and non-affected legs), gait and stance parameters are collected while the patient walks for 30 seconds on the treadmill with integrated sensor equipment (for measuring the force distribution).
Balance analysis with Biodex balance system SD: measurements of postural stability, fall risk, limits of stability, sensory integration are collected.
Gait and balance measurement
Virtual gait training procedures are included. Balance training procedures with Biodex Balance system are included too.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Gait and balance measurement
Virtual gait training procedures are included. Balance training procedures with Biodex Balance system are included too.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Age from 18 to 89 years old;
* Muscle strength according to the Oxford scale is 3-5 points;
* Able to walk without the help of others;
* Is able to communicate and understand instructions properly;
* Agrees to participate in the study (voluntary, explicit, informed written consent to participate).
Exclusion Criteria
* Unable to walk without the help of others;
* Sensorimotor aphasia or other perceptual disorders;
* Do not sign the informed consent.
18 Years
89 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Lithuanian University of Health Sciences
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ieva Žemaitienė
Ieva Žemaitienė, PT
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Eglė Lendraitienė, PhD
Role: PRINCIPAL_INVESTIGATOR
LUHS
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
LUHS hospital Kaunas Clinics Rehabilitation hospital of Kulautuva
Kaunas, , Lithuania
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
BE-2-67
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.