Viewing Study NCT06366542



Ignite Creation Date: 2024-05-06 @ 8:24 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06366542
Status: COMPLETED
Last Update Posted: 2024-07-03
First Post: 2024-03-25

Brief Title: Virtual Reality in People With Persistent Postural-Perceptual Dizziness
Sponsor: University of Jordan
Organization: University of Jordan

Study Overview

Official Title: The Effect of Using Virtual Reality on Balance in People With Persistent Postural-Perceptual Dizziness
Status: COMPLETED
Status Verified Date: 2024-07
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 aimed to compare the effectiveness of virtual reality VR and vestibular rehabilitation therapy VRT in enhancing balance in individuals with Persistent Postural-Perceptual Dizziness PPPD The experimental group received VR combined with VRT and optokinetic stimulation while the control group received VRT and optokinetic stimulation The study involved 42 individuals diagnosed with PPPD and administered ten intervention sessions over six weeks The study also examined the impact of VR on various aspects of PPPD including dizziness visual vertigo mental well-being sleep quality fall risk and overall quality of life
Detailed Description: Persistent Postural-Perceptual Dizziness PPPD represents a relatively new vestibular diagnosis that has garnered recent attention within the medical community Consequently there exists a pressing demand for efficacious and innovative management strategies The primary purpose of this study was to assess the comparative effectiveness of virtual reality VR versus vestibular rehabilitation therapy VRT in enhancing balance among individuals afflicted with PPPD A secondary purpose encompassed an investigation of VRs impact on various dimensions of PPPD including dizziness visual vertigo mental well-being sleep quality fall risk and overall quality of life Materials and Methods A cohort comprising forty-two individuals conclusively diagnosed with PPPD was randomly assigned to two distinct groups The experimental cohort comprised twenty-one participants subjected to a combination of VR with optokinetic stimulation alongside VRT whereas the control group also consisting of twenty-one individuals underwent solely optokinetic stimulation paired with VRT The intervention sessions were administered twice weekly over a span of six weeks resulting in a total of ten intervention sessions Additionally baseline and post-intervention assessments were conducted to gauge the efficacy of the interventions

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