Viewing Study NCT06169878



Ignite Creation Date: 2024-05-06 @ 7:51 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06169878
Status: COMPLETED
Last Update Posted: 2023-12-14
First Post: 2023-11-25

Brief Title: Efficiency of the Adjustable Lower Extremity Abduction Apparatus After Total Hip Replacement Surgery
Sponsor: Bahçeşehir University
Organization: Bahçeşehir University

Study Overview

Official Title: Evaluation of the Efficiency of the Adjustable Lower Extremity Abduction Apparatus After Total Hip Replacement Surgery
Status: COMPLETED
Status Verified Date: 2023-12
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: This study was conducted to evaluate the effect of the adjustable lower extremity abduction apparatus developed after total hip arthroplasty TKP surgeries on preventing dislocation and walkingThe study is of randomized controlled type It was held on the inpatient floor of a Training and Research Hospital in Istanbul between November 2021 and October 16 2023 with patients undergoing femoral neck fracture surgery

All patients who were admitted to this clinic for surgical intervention constituted the population of the study In the research 30 patients between the ages of 50-80 were included in the experimental group in which the Adjustable lower extremity abduction apparatus developed within the scope of the thesis was used and 30 patients in which this apparatus was not used were included in the control group As data collection tools in the study Patient Introduction Form Standardized Mini Mental State Test Patient Mobility Scale Modified Barthel Activities of Daily Living Index Apparatus Quality and Comfort Assessment Form and Harris Hip Score Form were used Data were evaluated using IBM SPPS 270 statistical package program
Detailed Description: This study aimed to evaluate the effect of an adjustable lower extremity abduction apparatus on the prevention of dislocation activities of daily life and gait after total hip replacement THR The study was a randomised controlled trial It was conducted on the inpatient floor of a Training and Research Hospital in Istanbul between November 2021 and 16 October 2023 with patients who had femoral neck fracture surgery All patients admitted to this clinic for surgical intervention constituted the population of the study In the study 30 patients aged 50-80 years were included in the intervention group using the adjustable lower extremity abduction apparatus developed within the scope of the thesis and 30 patients using the pillow in routine practice were included in the control group Patient Introduction Form Standardized Mini-Mental State Test Patient Mobility Scale Modified Barthel Activities of Daily Living Index Apparatus Quality and Comfort Assessment Form and Harris Hip Score Form were used as data collection tools Data were analysed using the IBM SPPS 270 software

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