The Validity and Reliability of a Wearable System for Assessing Turning Characteristics.

November 5, 2018 updated by: Yea-Ru Yang, National Yang Ming University
The Validity and Reliability of a Wearable System for Assessing Turning Characteristics.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Subjects are reclaimed to finish several turning task under different turning angle.

The wearable system is patched on both subjects' legs and waist, to assess turning characteristics under different turning angle.

Study Type

Interventional

Enrollment (Anticipated)

30

Phase

  • Not Applicable

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

  • Taiwan
      • Taipei, Taiwan, 112
        • Recruiting
        • National Yang-Ming University

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

20 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Able to walk 10 m independently without any device.

Exclusion Criteria:

  • Dizzy causing by eye disorders or vestibular disease.
  • Any disease which involved in gait performance.
  • Can't follow the order by investigator during task.

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

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Normal subjects
Other: Turning
start to walk with normal speed, and then turn to approach the terminal under different angle.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Turning step count
Time Frame: pre-test and post-test within a week
record numbers of step during turning
pre-test and post-test within a week
Turing time
Time Frame: pre-test and post-test within a week
record second which subject spend during turning
pre-test and post-test within a week
Stride length during turning
Time Frame: pre-test and post-test within a week
record the distance of bipedal stride length respectively
pre-test and post-test within a week
Walking speed approached turning
Time Frame: pre-test and post-test within a week
record the velocity and change of velocity before start turning
pre-test and post-test within a week
Turning angle
Time Frame: pre-test and post-test within a week
record the total turning angle and bipedal turning angle each step
pre-test and post-test within a week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

National Yang Ming University

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)

August 24, 2017

Primary Completion (Anticipated)

August 23, 2019

Study Completion (Anticipated)

August 23, 2019

Study Registration Dates

First Submitted

January 8, 2018

First Submitted That Met QC Criteria

January 14, 2018

First Posted (Actual)

January 23, 2018

Study Record Updates

Last Update Posted (Actual)

November 6, 2018

Last Update Submitted That Met QC Criteria

November 5, 2018

Last Verified

November 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • YM106038E

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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