Viewing Study NCT06647355



Ignite Creation Date: 2024-10-26 @ 3:43 PM
Last Modification Date: 2024-10-26 @ 3:43 PM
Study NCT ID: NCT06647355
Status: COMPLETED
Last Update Posted: None
First Post: 2024-10-06

Brief Title: Evaluation of the Effect of a Clinical Exercise Programme on Plantar Distribution and Correction of Postural Asymmetries
Sponsor: None
Organization: None

Study Overview

Official Title: Predicting Body Pain by Postural Related Problems in Middle-age and Older Adults Using Machine Learning
Status: COMPLETED
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study was to identify significant variables that contribute to the association between postural problems plantar pressure distribution and levels of bodily pain in middle-aged and elderly adults The researchers hypothesis is that plantar pressure characteristics and postural asymmetries differ according to gender are related to body composition and predict pain levels The study described here is the only one to include variables that make it possible to identify body asymmetries in a postural analysis based on the distribution of plantar pressure and body composition
Detailed Description: The study employed an observational cross-sectional design A convenience sample was recruited to analyse differences between men and women in anthropometrics body composition plantar pressure distribution and pain levels Without intervention researchers observed and recorded data at a single time point allowing comparisons between sexes and exploring correlations among the measured variables This type of design allowed a snapshot view of the differences and associations present within the sample

Study Oversight

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