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A Study for Collecting Data on the Motion Analysis of Stroke Patients

A Study for Collecting Data on the Motion Analysis of Stroke Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05916924
Enrollment
100
Registered
2023-06-23
Start date
2022-03-28
Completion date
2024-12-31
Last updated
2023-06-23

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

Conditions

Stroke

Brief summary

An observational study to collect (functional evaluation and daily motion) for composing 3D kinematic data that will be the basis for setting rehabilitation goal points for each stroke patient and developing virtual reality rehabilitation contents via video shooting.

Interventions

OTHERCollection of clinical data including manual muscle test (MMT), range of motion (ROM), Fugl-Meyer assessment (FMA), berg balance scale (BBS) and kinetic data via video shooting

Collection of clinical data including manual muscle test (MMT), range of motion (ROM), Fugl-Meyer assessment (FMA), berg balance scale (BBS) and kinetic data via video shooting

Sponsors

Bundang CHA Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1\. Inclusion criteria 1. Over 20 years of age 2. More than 1 month after onset of stroke 3. After hearing a detailed explanation of this study and fully understanding it, the subject or legal representative voluntarily decides to participate and agrees in writing to observe the precautions 2\.

Exclusion criteria

1. Patients who correspond to one or more of the following cannot participate in the study. 2. Patients with systemic infectious symptoms at the time of participation in the study 3. In the case of a person with impaired ability to consent (less than 10 points on the MMSE), a person without a guardian 4. Those with severe medical conditions such as unstable conditions in the cardiovascular system, digestive system, respiratory system, endocrine system, etc., and those with poor general health 5. Other cases where the researcher judges that participation in this study is not suitable (Patients who are participating in other studies or have participated in other studies within the past 30 days can also participate in this study.)

Design outcomes

Primary

MeasureTime frameDescription
Changes in motion analysis in gait spatiotemporal parametersChange from baseline to 1 day and 14 daysMotion analysis is a process of measuring and evaluating gait function in gait spatiotemporal parameter, gait speed (m/s)
Changes in motion analysis in kinematic parametersChange from baseline to 1 day and 14 daysMotion analysis is a process of measuring and evaluating gait function in kinematic parameter, sagittal angle (degree)

Secondary

MeasureTime frameDescription
Changes in manual muscle test (MMT)Change from baseline to 1 day and 14 daysMMT is a process of the evaluating the function and strength of individual muscles and muscle groups based on the effective performance of a movement in relation to the forces of gravity and manual resistance in score
Changes in motricity index (MI)Change from baseline to 1 day and 14 daysMI is a process of the evaluating the function and strength of upper, lower extremities and trunk in score
Changes in berg balance scale (BBS)Change from baseline to 1 day and 14 daysBBS is a measurement of balancing function. A five-point ordinal scale, ranging from 0-4. 0 indicates the lowest level of function and 4 the highest level of function. Total score = 56

Countries

South Korea

Contacts

Primary ContactHyun Jung Oh
a210525@chamc.co.kr+82 031 780 6003

Outcome results

None listed

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