The Alusti Test:Functional Evaluation Scale of Physical Performance in the Geriatric Population

Sponsor
Okan University (Other)
Overall Status
Completed
CT.gov ID
NCT04807556
Collaborator
(none)
75
1
10.9
6.9

Study Details

Study Description

Brief Summary

With the Alusti Test, which is created by Josu Alustiza Navarro considering the existing tests, the physical performances of geriatricians with different levels and cognitive capacity are evaluated in a very short time and without tiring the patient. There are 2 versions, short and full. The short version is applicable to 100% of the large population, including "and cases of cognitive impairment. With the full version, it has nearly 85-90% applicability."

However, there is no study regarding the English version and validity reliability of the 'Alusti Test.

For this purpose, it is to investigate the English validity and reliability of the functional assessment scale of physical performance (Alusti Test) for the geriatric population and to provide a measurement tool to be used in the English literature to the sciences who want to work in this field.

Condition or Disease Intervention/Treatment Phase
  • Other: Alusti Test

Study Design

Study Type:
Observational
Actual Enrollment :
75 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
The Alusti Test: Turkish Validity and Reliability Study of the "Functional Evaluation Scale of Physical Performance in the Geriatric Population".
Actual Study Start Date :
Nov 2, 2020
Actual Primary Completion Date :
Aug 30, 2021
Actual Study Completion Date :
Sep 30, 2021

Outcome Measures

Primary Outcome Measures

  1. Alusti test [5 minute]

    Physical and psychological functional conditions are key factors in the elderly population. Many evaluation tools are available, but they cannot be applied to the whole geriatric population. The use Alusti Test is presented.

Secondary Outcome Measures

  1. Short Physical Performance Battery (SPPB). [5 minute]

    Short Physical Performance Battery (SPPB) is an assessment test used to examine gait, balance, strength, and endurance in elderly epidemiological studies and outpatient clinics. Its performance is divided into three subtests: a hierarchical balance assessment, a short usual gait speed test, and 5 Time Sit to Stand (5TSTS) test

  2. TimedUp and Go (TUG). [3 minutes]

    It is a clinical assessment test widely used to assess balance and walking ability in elderly populations [19-21]. To perform this test, participants are observed and timed in seconds, while they rise from an armed chair of approximately 46cm seat height and 65 cm arm height, walk at their usual pace a distance of 3 meters towards a line marked on the floor, turn 180 degrees, walk back to the chair, and sit down

  3. Mini-Mental State Examination (MMSE) [3 minutes]

    Cognitive status was assessed using the Mini-Mental State Examination (MMSE); MMSE scores were categorized into three levels (0-17, 18-23, and 24-30, indicating severe, mild, and no impairment, respectively).

  4. Tinetti Test [5 minutes]

    The Tinetti test has been recommended and widely used in the elderly to assess mobility, balance and gait, and predict falls. D

  5. Rivermead Mobility Index [10 minute]

    The Rivermead Mobility Index (RMI) is a hierarchical mobility scale used in neurological rehabilitation. It includes 15 items related to bed mobility, transfers, walking, stair use, and running. The RMI is presented in a questionnaire format with the examiner required to make one observation (standing unsupported >10 s). All items are rated in a yes/no format with positive responses scoring a 1 for a maximal RMI score of 15.

  6. Barthel Index [5 minute]

    The Barthel index (BI) is a widely used observer-based instrument to measure physical function.

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being over the age of 65,

  • volunteering

  • to be able to read and write

  • To be able to read and write in Turkish

Exclusion Criteria:
  • None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Emine Atıcı Tuzla İstanbul Turkey

Sponsors and Collaborators

  • Okan University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emine Atıcı, Principal Investigator, Okan University
ClinicalTrials.gov Identifier:
NCT04807556
Other Study ID Numbers:
  • 004
First Posted:
Mar 19, 2021
Last Update Posted:
Jan 4, 2022
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jan 4, 2022