ClinicalTrials.gg
CompletedNCT04615533Updated Jan 21, 2022

Validity Reliability of FrailBESTest in Older Adults

An observational study in Frail Elderly Syndrome, Balance; Distorted and Assessment, Self, sponsored by Kırıkkale University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 65 Years to 95 Years. Per ClinicalTrials.gov, last updated 2022-01-21.

Sponsored by Kırıkkale University · Observational

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Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
140
Ages
65 Years to 95 Years
Sex
All
01

Study summary

Fraility; It is an age-related biological syndrome. It is characterized by decreased resistance to stressors due to changes in functional reserves and physiological systems.

BESTest, which is frequently used in the literature, was modified and Frail'BESTest was developed to detect balance problems in fragile individuals. The test consists of 6 subtitles. These are participation, reaction, movement ability, sensory organization, biomechanical constraints, gait symmetry. When looking at the literature, the Turkish version of Frail'BESTest has not been found. For this reason, the aim of study is to examine the validity and reliability of the Turkish version of Frail'BESTest in elderly individuals and to question the effectiveness of its clinical use and to bring it to the use of other researchers.

Read the detailed description

Fraility; It is an age-related biological syndrome. It is characterized by decreased resistance to stressors due to changes in functional reserves and physiological systems.Especially, the increase in the incidence of falls, loss of mobility, dependence in basic life activities, increase in hospitalizations and increased incidence of death make the diagnosis and treatment of frailty important in elderly individuals.

BESTest, which is frequently used in the literature, was modified and Frail'BESTest was developed to detect balance problems in fragile individuals. The test consists of 6 subtitles. These are participation, reaction, movement ability, sensory organization, biomechanical constraints, gait symmetry. When looking at the literature, the Turkish version of Frail'BESTest has not been found. For this reason, the aim of study is to examine the validity and reliability of the Turkish version of Frail'BESTest in elderly individuals and to question the effectiveness of its clinical use and to bring it to the use of other researchers.

02

Conditions studied

  • Frail Elderly Syndrome
  • Balance; Distorted
  • Assessment, Self
03

In context

Lead sponsor

Kırıkkale University is the lead sponsor of 114 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
65 Years to 95 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Individuals aged 65 and over, Volunteering to participate in research, No cooperation and communication problem

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Individuals aged 65 and over,

    • Your willingness to participate in research Elderly individuals with a diagnosis of frailty
    • No cooperation and communication problems

Exclusion criteria

Exclusion Criteria:

  • Individuals with neurological and orthopedic problems Uncontrollable hypertension

    • Those with cardiac disease
    • Those with cooperation and communication problems
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
140 participants (actual)
Patient registry
No

Groups and cohorts

  • Frail older adults, assessment

    Frail older adults, assessment Frail'BESTest, Clinical Frailty Scale, Mini BESTest, Berg Balance Scale, Tinetti Blance and Gait Scale

    Other: Frail older adults, assessment

Interventions

  • OtherFrail older adults, assessment

    Frail'BESTest, Clinical Frailty Scale, Mini BESTest, Berg Balance Scale, Tinnetti Balance and gait sacale

06

What researchers measure

Primary outcomes

  1. Frail'BESTest

    The test consists of 6 subtitles. These are participation, reaction, movement ability, sensory organization, biomechanical constraints, gait symmetry.

    Time frame: Day 1

  2. Clinical Frailty Scale

    Scale evaluates physical weaknesses such as comorbidity, cognitive impairment, and disability. Scale scoring is from 1 (very favorable) to 9 (terminally ill)

    Time frame: Day 1

  3. Mini BESTest

    The Mini-BESTest consists of 14 items and evaluates 4 different components of dynamic balance (1) antispatient postural adjustments, (2) reactive postural control, (3) sensory orientation and (4) dynamic walking).

    Time frame: Day 1

  4. Berg Balance Test

    The BBS consists of 14 items to directly monitor the maintenance of body balance during performance

    Time frame: Day 1

  5. Tinetti Balance and Gait Test

    In the test used to evaluate balance, walking score is maximum 12 points, balance score is maximum 16 points and a total of 28 points

    Time frame: Day 1

07

Study locations

1 site
  • Ayşe Abit Kocaman
    Kirikkale, 7110, Turkey (Türkiye)
08

References and documents

Publications

  • Kubicki A, Brika M, Coquisart L, Basile G, Laroche D, Mourey F. The Frail'BESTest. An Adaptation of the "Balance Evaluation System Test" for Frail Older Adults. Description, Internal Consistency and Inter-Rater Reliability. Clin Interv Aging. 2020 Jul 30;15:1249-1262. doi: 10.2147/CIA.S247332. eCollection 2020. PubMed 32801673 ↗

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Oct 2020 to primary completion in Jan 2022, 14 months.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 29, 2020
First posted
Nov 4, 2020
StartActual
Oct 25, 2020
Primary completionActual
Jan 1, 2022
CompletionActual
Jan 1, 2022
Last update
Jan 21, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jan 21, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04615533
Responsible party
Ayşe Abit Kocaman (Principal Investigator, Kırıkkale University) — Principal investigator
First posted
Nov 4, 2020
Start date
Oct 25, 2020
Primary completion
Jan 1, 2022
Completion
Jan 1, 2022
Last update
Jan 21, 2022

Study contacts

Ayşe Abit Kocaman
principal investigator · Kırıkkale University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2022. You cannot join it, but the record below documents what was studied.

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