Postural Analysis of Patients Receiving Rehabilitation Program

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

Status

Completed

Conditions

Intervention / Treatment

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

      • Kaohsiung, Taiwan, 807
        • aohsiung Medical University Chung-Ho Memorial Hospital

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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