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The Cycling Exercise With Virtual Reality Visual Stimulation for Rehabilitation in CVA Patients

Institutional Review Board of Chung Shan Medical University Hospital

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02069691
Enrollment
13
Registered
2014-02-24
Start date
2012-08-31
Completion date
2013-05-31
Last updated
2014-02-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

stroke,, rehabilitation,, leg cycling,, feedback,, virtual reality

Brief summary

Background: Hemiplegia is one of the main reasons why stroke survivors lose their walking and balancing ability. Many studies point out that cycling is an effective means for lower limb rehabilitation. However, during training, the unaffected limb may compensate for the affected one resulting in suboptimal rehabilitation. To address this issue, the investigators developed the virtual reality-cycling training system (VRCTS) which can acquire force and speed signals in real-time through a cycling module. The system then analyzes the acquired data and uses a 3D VR rehabilitation program to help patients to train their affected side. The aim of the study was to develop the VRCTS, verify its function and test system function on both normal subjects and stroke patients. Methods: In this system, the investigators designed a cycling device that is embedded with load cell and encoder sensors to detect cycling force and angle in real-time. A Cycling Graph User Interface Control and Data Recode System (Cycling CR System) was applied for signal analysis and feedback control. The investigators designed a 3D interactive VR rehabilitation program that can guide and train the users through visual feedback. Each user performed a pre-test to examine determine condition, left-right balance and other parameters, which allows the system to be customized.

Interventions

DEVICEvirtual reality-cycling training system

Sponsors

Chung Shan Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
25 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* single stroke with unilateral hemiplegia (Brunnstrom stage III); * hypertonia in the affected leg, modified Ashworth scale (MAS) grade ≦ 2; * no significant perceptual, cognitive, or sensory deficits; * no history of osteoarthritis, severe cardiopulmonary disease, or vascular disease in lower limbs * lack of a fixed contracture in the affected lower limb

Design outcomes

Primary

MeasureTime frame
pedal force of affected legup to 24 weeks

Secondary

MeasureTime frame
asymmetrical ratio indexup to 24 weeks

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026