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Vestibular Diseases clinical trials

View clinical trials related to Vestibular Diseases.

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NCT ID: NCT06350721 Not yet recruiting - Physical Disability Clinical Trials

Feasibility, Usability and Safety of the Vestibular Rehabilitation Using the Immersive Virtual Reality Software DizzyVR

DizzyVR
Start date: April 1, 2024
Phase: N/A
Study type: Interventional

The goal of this pilot study is to assess the safety and feasibility of the immersive virtual reality system called DizzyVR in participants diagnosed with a vestibular disorder. The main questions it aims to answer are: - To assess the feasibility, usability and safety of the system DizzyVR for the vestibular rehabilitation in participants with vestibular disorders. - To detect and record possible adverse events due to the use of DizzyVR. - To examine the degree of adherence of the participants to the intervention. - To know the average success rate of the different games in each session. - To evaluate the average difficulty levels overcome throughout the intervention. - To know the usability and satisfaction with the system reported by participants and therapists. Participants will receive the vestibular rehabilitation based on the novel immersive virtual systema, DizzyVR.

NCT ID: NCT06350669 Not yet recruiting - Vestibular Disorder Clinical Trials

App-supported Vestibular Rehabilitation (RCT)

Start date: June 2024
Phase: N/A
Study type: Interventional

A randomized controlled trial to assess the efficacy of an app-assisted vestibular rehabilitation in increasing adherence to VR and treatment outcomes

NCT ID: NCT06300840 Not yet recruiting - Vestibular Disorder Clinical Trials

Vibrotactile Feedback Belt in Patients With Unilateral Vestibular Hypofunction (UVH)

VIBE
Start date: March 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to study the impact of a continuous vibrotactile feedback belt on balance, (fear of) falling, fatigue and overall functioning in participants with chronic disabling unilateral vestibular hypofunction. The main questions it aims to answer are: • does wearing a vibrotactile feedback belt during waking hours for a week improve sense of balance and mobility, fear of falling, fatigue and overall functioning • does wearing a vibrotactile feedback belt influence static and dynamic balance and gait performance during balance and gait testing. Participants will goes through different phases in an randomized order; a baseline phase, a sham phase (i.e., wearing the BalanceBelt while it is switched off) and an intervention phase (i.e., wearing the BalanceBelt while it is switched on). It is expected that, just as with patients with bilateral loss of the balance organ, patients with a unilateral loss will also benefit from the BalanceBelt.

NCT ID: NCT06229717 Not yet recruiting - Children, Only Clinical Trials

Vestibular and Postural Function in an Unselected Group of Children With Sensorineural Hearing Loss

VASIC
Start date: August 2025
Phase:
Study type: Observational

The goal of this prospective cohort study is to investigate the vestibular function in children with unilateral or bilateral sensorineural hearing loss. The main hypothesis of the study is that abnormal vestibular test results will be found in 20-30 % of the children with sensorineural hearing loss. The participants will be children in the age of 3-10 years with sensorineural hearing loss. The test protocol consists of questionnaires and vestibular and postural assessments.

NCT ID: NCT06229704 Not yet recruiting - Children, Only Clinical Trials

Vestibular and Postural Function in Children Suspected of Balance Disorders

VASIC
Start date: January 2025
Phase:
Study type: Observational

The goal of this prospective cohort study is to investigate the vestibular function in children suspected of balance disorders, and to follow up on their balance progressions after rehabilitation. The main hypothesis of the study is that delayed gross motor development and symptoms of dizziness and balance problems in some children are caused by vestibular dysfunction. The investigators expect that early detection and rehabilitation by a physiotherapist will improve the balance ability for the child. The participants will be children in the age of 6 months to 10 years with delayed gross motor development and/or with dizziness/balance problems. The test protocol consists of questionnaires, hearing screening and vestibular and postural assessments.

NCT ID: NCT06177132 Not yet recruiting - Vestibular Disorder Clinical Trials

Vestibular Infant Screening - Rehabilitation

VIS-REHAB
Start date: November 2025
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to investigate the short-term effect of a structured, combined postural control and gaze stabilisation protocol (VIS-REHAB protocol) in a group of vestibular-impaired children of different age categories (3-17 years). The main questions it aims to answer are: - What is the short-term effect of the VIS-REHAB protocol? - What are the most important factors that may influence the effect of and outcome after application of the VIS-REHAB protocol? The participant will undergo both an active rehabilitation program (VIS-REHAB protocol) and a period during which physical therapy is discontinued (CTRL protocol).: - VIS-REHAB protocol: Postural control (static and dynamic postural stability exercises), gaze stability exercises (oculomotor function and VOR-exercises) & general gross motor training with focus on gaze stability and postural control. Researchers will compare the VIS-REHAB protocol with receiving no therapy (CTRL protocol) to evaluate potential enhancements in postural stability, gaze stability, motor performance and quality of life.

NCT ID: NCT06143462 Not yet recruiting - Vestibular Disorder Clinical Trials

Vestibular Rehabilitation for Unsteadiness After Intratympanic Gentamicin in Patients With Meniere's Disease

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

To investigate the efficacy of vestibular rehabilitation treatment on unsteadiness after intratympanic gentamicin in patients with Meniere's disease.

NCT ID: NCT05865769 Not yet recruiting - Pulmonary Disease Clinical Trials

Impact of Pulmonary Function on Vestibular System in Children

Start date: December 20, 2023
Phase:
Study type: Observational

The vestibular system and the pulmonary system are two critical components of the human body that are involved in maintaining balance, coordination, and the exchange of oxygen and carbon dioxide This study aim to investigate the impact of pulmonary function on the vestibular system in children. Children aged 4 to 10 years will be recruited from Future Academy School in March 2023. Pulmonary function will be measured using digital spirometry, and balance will be evaluated using the Mini-SITCIB test, which tested vision, proprioception, and the vestibular system using mobile sensors fixed near the center of gravity. Features from the sensor data will be extracted using Python 3.10 code, and the SPSS program will used to compare these features between the two groups.

NCT ID: NCT05831618 Not yet recruiting - Rehabilitation Clinical Trials

New Rehabilitation Protocol for Patients With PPPD

Start date: July 30, 2023
Phase: N/A
Study type: Interventional

The investigators will test a new rehabilitation protocol on patients with persistent postural perceptual dizziness (PPPD). The investigators hypothesize that patients with PPPD, in the absence of vestibular deficits, do not benefit from standard vestibular rehabilitation but instead need a rehabilitation that acts on visual and postural stability, through training of saccadic movements in dynamic contexts of cognitive-motor dual-task and rehabilitation of postural stability.

NCT ID: NCT05424302 Not yet recruiting - Clinical trials for Benign Paroxysmal Positional Vertigo

Effect of Peripheral Vestibular Disease Location on Outcomes Following Home-based Virtual Reality Vestibular Therapy

VR-PVD-RCT
Start date: January 2023
Phase: N/A
Study type: Interventional

This parallel-group randomized controlled trial aims to determine if the location of the lesion(s) in the vestibular system (unilateral versus bilateral, lateral semi-circular canal versus otolith) impacts the effectiveness of adjunct take-home head-mounted display (HMD) virtual reality (VR) therapy in improving patient symptomatology. Fifty patients meeting inclusion criteria will be recruited from the principal investigator's neurotology clinic. Baseline symptomatology questionnaires will be completed, followed by random allocation to virtual reality and control groups. Vestibular rehabilitation and virtual reality protocols will be adhered to for 4 to 8 weeks, followed by symptomatology questionnaires. Data analysis will be conducted to answer the study's objectives.