Reliability and Validity of the Elderly Mobility Scale, French Version

October 26, 2017 updated by: Pole Santé Plouasne Saint Pern Becherel

Reliability and Validity of the Elderly Mobility Scale for Frailty People Living at Home, French Version

This study evaluates the reliability of the French version of the "elderly mobility scale" and its correlation with the "frailty elderly scale "

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

The research question:

How to effectively measure the physical independence of the elderly at home and how, from this measure, the investigators can determine the fragility threshold of the elderly.

The elderly mobility scale measures the critical points of the patient's physical autonomy. This scale was developed in Great Britain. The purpose of this study is to establish the reliability of this French version scale and to study the correlation with the elderly scale fragility.

People are recruited by a Medical consultant. After consent, their frailty is measured and a prescription is done to see a Physical therapist. The physical therapist will evaluate the physical points measured/ mentioned in the Elderly Mobility Scale, twice in a week, with two different assessors.

Study Type

Observational

Enrollment (Actual)

25

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
      • Becherel, France, 35190
        • Cabinet Medical
      • Plouasne, France, 22830
        • Cabinet Medical
      • Saint Pern, France, 35190
        • Cabinet de kinésithérapie

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

68 years and older (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

People living in their home, more than 70 years old, alone or not.

Description

Inclusion Criteria:

  • living at home, more than 70 years old

Exclusion Criteria:

  • current recovery for orthopaedic problems
  • Cognition impairment
  • all acute problems with an impairment of mobility

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: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
inter-rater Reliability
Time Frame: Time Frame: Up to One week
intraclass correlation coefficient with data : Elderly Mobility Scale score between rater one and rater two
Time Frame: Up to One week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Concurrent Validity
Time Frame: Time Frame: Up to One week
correlation coefficient between Elderly Mobility Scale and Frailty scale
Time Frame: Up to One week
sensibility and specificity
Time Frame: Time Frame: Up to One week
sensibility and specificity of Elderly Mobility Scale regarding Frailty
Time Frame: Up to One week
Receiver Operating Curve and cut-off score
Time Frame: Time Frame: Up to One week
Determination of a cut-off score for Elderly Mobility Scale as a screening tool to detect the frailty by use of Receiver Operating Characteristics curve
Time Frame: Up to One week

Collaborators and Investigators

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

Sponsor

Pole Santé Plouasne Saint Pern Becherel

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

March 21, 2017

Primary Completion (Actual)

October 26, 2017

Study Completion (Actual)

October 26, 2017

Study Registration Dates

First Submitted

December 16, 2016

First Submitted That Met QC Criteria

December 29, 2016

First Posted (Estimate)

January 2, 2017

Study Record Updates

Last Update Posted (Actual)

October 30, 2017

Last Update Submitted That Met QC Criteria

October 26, 2017

Last Verified

October 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • PSPB-01-2016

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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