Association Between Gait Assessed by Intelligent System and Cognitive Function in Silent Cerebrovascular Disease

NCT04456348 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1600

Last updated 2020-07-02

No results posted yet for this study

Summary

This study is a multi-center prospective cohort study. We will continuously recruit subjects with silent cerebrovascular disease aged 60 to 85 years from Shanghai and Guizhou. Data including demographic characteristics, medical history, other concomitant diseases, neurological function assessments, laboratory examinations, imaging examinations, and other clinical data and health economics survey responses will be collected from all subjects.

At baseline, all subjects will undergo gait assessment using the intelligent system and cognitive function scale assessment by clinicians. According to the intelligent gait results, the subjects will be divided into normal and abnormal gait groups. All subjects will be observed naturally for 1 year, and all medical behaviors will be recorded. All subjects will be interviewed by telephone for the occurrence of vascular events and changes in medical behaviors at half a year after enrollment and followed up at 1 year after enrollment, including gait evaluation using the intelligent system and cognitive function scale evaluation by clinicians. During the follow-up period, patients can visit the hospital for follow-up at any time when their condition changes.

Conditions

  • Silent Stroke

Interventions

OTHER

there is no intervention

There is no intervention

Sponsors & Collaborators

  • The Affiliated Hospital Of Guizhou Medical University

    collaborator OTHER
  • Fudan University

    collaborator OTHER
  • Shanghai Zhongshan Hospital

    lead OTHER

Principal Investigators

  • Jing Ding, MD · Shanghai Zhongshan Hospital

Eligibility

Min Age
60 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-01
Primary Completion
2021-10-31
Completion
2021-12-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04456348 on ClinicalTrials.gov