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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02207933
Other study ID # 4-2013-0270
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2013
Est. completion date July 2014

Study information

Verified date December 2014
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To investigate the effect of anteroposterior weight shifting training with visual biofeedback on step length asymmetry. Reduced speed and asymmetry of stepping is a specific characteristic of hemiplegic gait. Asymmetry of stepping is characterized by shorter step length of the unaffected limb compared to the affected limb. Causes of this phenomenon are difficulty in weight bearing at the affected limb, weak propulsive force of the affected limb, and decreased strength of hip extensors. To correct these factors. we have developed an anteroposterior weight shifting training system with visual feedback and studied its effects.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date July 2014
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

1. Independent standing

2. Ability to walk 10m without manual assistance

3. Asymmetric ratio of step length > 1.1

4. No severe perceptual, cognitive or cardiovascular impairments that could affect walking

Exclusion Criteria:

1. Quadriplegia or double hemiplegia

2. Orthopedic or neurologic conditions in addition to the stroke

3. Had more than 1 cerebrovascular accident

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
AP shifting training
AP shifting training in addition to gait training 3 times a week for 6 weeks
Gait training
Gait training only for 3 times a week for 6 weeks.

Locations

Country Name City State
Korea, Republic of Severance hospital 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 change of step Length Asymmetric Ratio paretic step length/non paretic step length baseline, 3 weeks, 6 weeks, 12 weeks
Secondary change of Step Length Asymmetric Index paretic step length-non paretic step length/0.5[paretic step length +non paretic step length baseline, 3 weeks, 6 weeks, 12 weeks
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