- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05663229
Postural Analysis of Patients Receiving Rehabilitation Program
October 20, 2023 updated by: Kaohsiung Medical University Chung-Ho Memorial Hospital
Kaohsiung Medical University Chung-Ho Memorial Hospital
This is a study for evaluation of posture of patients with neurological disease in rehabilitation department.
Study Overview
Detailed Description
In this study, we evaluate the static posture stability of the patient, such as during sitting, standing and dynamic posture stability of the patient, such as during walking, time-up-and-go test.
Study Type
Observational
Enrollment (Actual)
13
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Kaohsiung, Taiwan, 807
- aohsiung Medical University Chung-Ho Memorial Hospital
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years to 81 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Patient with physical disability followed-up in rehabilitation department
Description
Inclusion Criteria:
- Patient with physical disability followed-up in rehabilitation department
Exclusion Criteria:
- Patients with congitive impairment that can't complete the evalaution well
- Patients with uncontrolled comorbidity diseases
- Attended other study in recent 3 months
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Experimental group-with rehabilitation intervention
We evaluate the static or dynamic posture stability of patients with rehabilitation intervention
|
We evaluate the difference of with or without ankle foot orthosis
|
|
Control group-without rehabilitation intervention
We evaluate the static or dynamic posture stability of patients without rehabilitation intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Displacement of center of gravity during standing
Time Frame: 1 day
|
Data collected by motion analysis system
|
1 day
|
|
Displacement of center of gravity during walking
Time Frame: 1 day
|
Data collected by motion analysis system
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Trunk movement
Time Frame: 1 day
|
Data collected by motion analysis system
|
1 day
|
|
Hip movement
Time Frame: 1 day
|
Data collected by motion analysis system
|
1 day
|
|
Knee movement
Time Frame: 1 day
|
Data collected by motion analysis system
|
1 day
|
|
Ankle movement
Time Frame: 1 day
|
Data collected by motion analysis system
|
1 day
|
|
Foot pressure
Time Frame: 1 day
|
Data collected by Pedar (foot pressure system)
|
1 day
|
|
Foot reaction force
Time Frame: 1 day
|
Data collected by Pedar (foot pressure system) and force plate
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Yu Hsuan Tseng, Kaohsiung Medical University Chung-Ho Memorial Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2022
Primary Completion (Actual)
December 15, 2022
Study Completion (Actual)
July 28, 2023
Study Registration Dates
First Submitted
December 15, 2022
First Submitted That Met QC Criteria
December 22, 2022
First Posted (Actual)
December 23, 2022
Study Record Updates
Last Update Posted (Actual)
October 23, 2023
Last Update Submitted That Met QC Criteria
October 20, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- KMUHIRB-E(II)-20220039
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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