Vestibular Rehabilitation Aid for Dizziness Recovery
Vestibular Rehabilitation Aid
+ Standard of care vestibular rehabilitation
Brain Injuries, Traumatic+17
+ Brain Concussion
+ Brain Diseases
Treatment Study
Summary
Study start date: January 15, 2025
Actual date on which the first participant was enrolled.The study is exploring a new application called VestAid, which is designed to help people recover from dizziness. The goal is to see if using VestAid can provide the same or even quicker recovery compared to traditional methods of vestibular rehabilitation exercises. This is important because dizziness can significantly affect daily life, and finding more effective ways to manage it could improve the quality of life for many individuals. The study is targeting people who experience dizziness and are undergoing vestibular rehabilitation. Participants in the study will use the VestAid application, which may involve following specific exercises or guidelines through the app. The effectiveness of VestAid will be compared to usual care methods, assessing how quickly and effectively participants recover from dizziness. The study does not specify the method of application, such as whether exercises are guided through visual or audio instructions, but it aims to determine whether this digital approach can match or exceed standard treatments in terms of recovery time and effectiveness.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 60 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location