Time Up and go in Hemiplegic Patients (TUG)

February 3, 2015 updated by: Nicolas ROCHE, Centre d'Investigation Clinique et Technologique 805

Quantification of Biomechanical Parameters of Functional Task Time Up and Go in Hemiplegic Patients

Investing the Timed Up and Go (TUG) Test in Hemiplegic Patients Using 3D Motion Analysis

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The timed up and go is a routine quick test assessing motor functional tasks including stand up ,walk 3 m,turn around and sitting down.We will included hemiplegic patients to quantify biomechanic parameters

Study Type

Observational

Enrollment (Actual)

60

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

  • France
      • Garches, France, 92380
        • Hopital Raymond Poincare

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

60 hemiplegic out patients

Description

Inclusion Criteria:

  • Patients performing 3D gait analysis
  • Male or female adults aged ≥ 18 years,
  • Hemiplegia following unique stroke- Patients with hemiplegia able to stand up alone,walk and turn around alone without assistance.

Exclusion Criteria:

  • Patient with a protective measure,
  • Pregnant women, breastfeeding
  • Brain damage bilateral cerebellar syndrome, apraxia and / or severe aphasia,
  • Patient who received botulinum toxin injection in the 3 months prior to inclusion, patients who underwent surgery of the locomotor system in the 6 months prior to inclusion,
  • No affiliation to a social security
  • other pathology, complications with significant impact on the activities of walking.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Hemiplegic subjects
60 hemiplegic outpatients walking test
Other: Walking test
Other Names:
  • The TUG test included stand up ,walk,turn around ,sit down

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Variability of the center of mass
Time Frame: 1 hour
subjects will perform the TUG test with 3D walk analysis equipment
1 hour

Collaborators and Investigators

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

Sponsor

Centre d'Investigation Clinique et Technologique 805

Investigators

  • Principal Investigator: Nicolas ROCHE, MDPHD, Hopital Raymond Poincare

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

March 1, 2013

Primary Completion (Actual)

March 1, 2013

Study Completion (Actual)

November 1, 2014

Study Registration Dates

First Submitted

March 7, 2013

First Submitted That Met QC Criteria

March 7, 2013

First Posted (Estimate)

March 8, 2013

Study Record Updates

Last Update Posted (Estimate)

February 4, 2015

Last Update Submitted That Met QC Criteria

February 3, 2015

Last Verified

January 1, 2014

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2012-A01619-3

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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