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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04637737
Other study ID # 4-2014-0383
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 1, 2014
Est. completion date June 2021

Study information

Verified date November 2020
Source Yonsei University
Contact Deog Young Kim
Phone +82-2-2228-3714
Email KIMDY@yuhs.ac
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Asymmetric gait patterns of stroke is one of the most important functional activities to enable community participation, it is major goal for stroke patients. Reported that the stroke patients had asymmetry at stance time, single stance, double support time, and swing time compared to normal people, and claimed that the most important factor was step length. According to Albert et al., patients with an asymmetric gait pattern have a long double support phase and a healthy side single support phase, and less weight shift to the affected side. Recent studies have shown that visual feedback for weight shift may be helpful to obtain a symmetrical posture after stroke. However, no study has been conducted on the therapeutic effect on gait asymmetry and patterns. We aimed to investigate the effect of Anterioposterior Weight Shifting Training with Visual Biofeedback in subacute post-stroke patients on gait asymmetry and pattern. 40 subacute post-stroke patients with Step Length Asymmetry were enrolled in this study. The subjects were randomly assigned into two groups. The training group received an additional anterioposterior weight shifting training with visual Biofeedback 5 times per week for 4weeks. The control group received the usual gait training. The spatiotemporal and kinematic data were obtained during walking through 3D motion analysis. Functional Ambulation Category, Self-selected walking speed, Maximum safe walking speed, Berg balance Test (BBT), Fugl-Meyer Assessment (FMA), Medical Research Council Score (MRC), Functional Independent Measure-mobility, Timed Up and Go test (TUG) were assessed at pre, during, post- training, and 4week follow-up. Those were compared between two groups by repeated measures ANOVA.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date June 2021
Est. primary completion date June 2021
Accepts healthy volunteers No
Gender All
Age group 19 Years to 90 Years
Eligibility Inclusion Criteria: 1. less than 6 months after onset of the stroke 2. can stand and walk independently 10m 3. K-MMSE score of at least 15 4. have asymmetrical gait pattern with Step length asymmetric ratio greater than 1.1 5. over 20 years of age. Exclusion Criteria: 1. quadriplegia 2. past history of stroke 3. past history of Musculoskeletal disease or history of Neurological diseases

Study Design


Related Conditions & MeSH terms


Intervention

Device:
anterioposterior Weight Shifting Training with Visual Biofeedback
The training group received an additional anterioposterior weight shifting training with visual Biofeedback 5 times per week for 4weeks. AP training is made to instantly know your training status during training by measuring and processing the foot pressure in real time using the F-Scan (Tekscan) hardware system and Software Development Kit (SDK). Before training, all patients are instructed to place both feet at shoulder width, place the inverted foot approximately 30 cm in front of the unaffected side foot, move the body forward with the chest straight in an upright position, and be instructed to put the weight on the affected side. On the screen shown, measure the maximum weight distribution during the first 10 times and set the value added by 5% as the target value. It is designed to induce the maximum weight shift through the archery game.
Behavioral:
Conventional therapy
The control group received the usual gait training.

Locations

Country Name City State
Korea, Republic of Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Step Length Asymmetric Ratio Step Length Asymmetric Ratio = paretic step length/non paretic step length before training(0week)
Primary Step Length Asymmetric Ratio Step Length Asymmetric Ratio = paretic step length/non paretic step length during training(2week)
Primary Step Length Asymmetric Ratio Step Length Asymmetric Ratio = paretic step length/non paretic step length after training(4week)
Primary Step Length Asymmetric Ratio Step Length Asymmetric Ratio = paretic step length/non paretic step length Follow up(8week)
Primary Step Length Asymmetric Index Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length] before training(0week)
Primary Step Length Asymmetric Index Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length] during training(2week)
Primary Step Length Asymmetric Index Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length] after training(4week)
Primary Step Length Asymmetric Index Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length] Follow up(8week)
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