The Effect of Rehabilitative Games With SmartPose on Upper Extremity Recovery in Stroke Patients
NCT ID: NCT06778525
Last Updated: 2026-01-22
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.
COMPLETED
NA
34 participants
INTERVENTIONAL
2025-01-11
2025-06-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
* Does the use of rehabilitative games with the SmartPose application work to treat upper extremity motor, functional, and sensory recovery in stroke patients?
Researchers will compare the experimental group with the control group, which receives only conventional exercises with proven effectiveness, to determine whether SmartPose has an effect on upper extremity motor, functional, and sensory recovery in stroke patients.
The experimental group will receive 30 minutes of neuromuscular therapy and 30 minutes of SmartPose, 3 times a week for 8 weeks.
The control group will receive 60 minutes of neuromuscular therapy, 3 times a week for 8 weeks.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Telerehabilitation-Based Early Upper Extremity Training in Stroke Patients
NCT06261099
Exoskeleton-assisted Upper Limb Rehabilitation After Stroke
NCT04353622
The Effects of Neurorehabilitation Approaches Involving Different Upper Extremity Reactive Trainings in Stroke Patients
NCT06086314
Effects of Robot-Assisted Upper Extremity Training on Cognitive and Physical Functions After Stroke
NCT04335422
A Feasible Smart Upper Limb Rehabilitation Model for Patients With Stroke and Spinal Cord Injuries
NCT06215625
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.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experimental Group
A one-hour exercise protocol will be administered in this group, consisting of 30 minutes of conventional exercises and 30 minutes of Smartpose exercises.
Exercise
Personalized neuromuscular exercises, according to the patient's specific needs.
SmartPose
Virtual reality application containing rehabilitative games developed for individuals in need of exercise.
Control
A one-hour conventional exercise program will be administered to this group.
Exercise
Personalized neuromuscular exercises, according to the patient's specific needs.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Exercise
Personalized neuromuscular exercises, according to the patient's specific needs.
SmartPose
Virtual reality application containing rehabilitative games developed for individuals in need of exercise.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Age between 35 and 75 years
* Medical condition sufficiently stable to allow participation in active rehabilitation
* Brunnstrom Upper Extremity Stage ≥ 3
* Minimum sixth week post-stroke
* Ability to perform shoulder abduction and flexion against gravity with a minimum of 20°
Exclusion Criteria
* Modified Ashworth Scale score of 4 or 5
* Inability to maintain independent sitting balance
* Visual impairment or loss that prevents the perception of visual materials
35 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Istanbul University - Cerrahpasa
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Cilen Tavsanoglu
Physiotherapist
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Istanbul University-Cerrahpasa, Faculty of Health Science
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Msc thesis
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.