Viewing Study NCT05853406



Ignite Creation Date: 2024-05-06 @ 6:59 PM
Last Modification Date: 2024-10-26 @ 2:58 PM
Study NCT ID: NCT05853406
Status: RECRUITING
Last Update Posted: 2023-11-18
First Post: 2023-05-01

Brief Title: Determination of a Minimal Clinically Important Difference of the Functional Reach Test in the Elderly
Sponsor: Pole Sante Grace de Dieu
Organization: Pole Sante Grace de Dieu

Study Overview

Official Title: Determination of a Minimal Clinically Important Difference of the Functional Reach Test in the Elderly
Status: RECRUITING
Status Verified Date: 2023-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The main objective of the study is to determine the Minimal Clinically Important Difference of the Functional Reach Test in the Elderly by a statistical method

The first secondary objective of the study is to determine the Minimal Clinically Important Difference by the Anchor method based on a qualitative assessment by the patients of their own response The second secondary objective is to determine the Minimal Clinically Important Difference by the Delphi method based on the search for a consensus between physiotherapists specializing in geriatrics
Detailed Description: The French population is aging and geriatric rehabilitation care must adapt to this growing population The functional reach test is a common clinical test in geriatrics It helps to determine the risk of falling However its metrological qualities are not all determined The Minimal Clinically Important Difference MCID is in particular unknown for this test The MCID of a test makes it possible to personalize in a way more in-depth evaluation of physiotherapy treatment So it is necessary to characterize this essential metrological determinant of a common balance skills assessment tool

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None