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Clinical Trials/NCT04987502
NCT04987502
Completed
Not Applicable

Virtual Reality and Subjective Tinnitus

Assistance Publique - Hôpitaux de Paris1 site in 1 country120 target enrollmentSeptember 7, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Tinnitus
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
120
Locations
1
Primary Endpoint
Subjective Tinnitus Severity Scale (S.T.S.S.)
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to test if virtual reality immersion has the potential to significantly decrease subjective tinnitus intrusiveness when compared to standard care.

Detailed Description

This is a randomised controlled study aimed at further validating the use of Virtual Reality in the field of subjective tinnitus management. Indeed, earlier results have suggested that this innovative strategy has the potential to be as efficient as a Cognitive and Behavioural Therapy. Before the sessions, an automated tinnitus matching procedure will help create a sound similar to the tinnitus percept ("Tinnitus Avatar"). During the sessions (8 sessions; 30 minutes), the "Tinnitus Avatar" will be displayed auditorily but also visually - as a sparkling spot - in a variety of virtual 3D auditory and visual environments. In these virtual environments the patients will be given the possibility to voluntarily control and manipulate the "Tinnitus Avatar" by the means of a wand on top of which the sound and the sparkling will be attached. They will also be able to freely navigate in the virtual scenes where environmental sound will be displayed. Then the patients will be able to displace at will the "Tinnitus Avatar" in their peri-personal space or mask it by getting close to sounds they may encounter in the virtual scenes. It is supposed that regaining and training a capacity of interaction with the "Tinnitus Avatar" as if it were a standard sound will help recalibrate the attentional processes involved in tinnitus perception and then to decrease tinnitus intrusiveness.

Registry
clinicaltrials.gov
Start Date
September 7, 2022
End Date
May 31, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age \> 18 years and \< 75 years,
  • French speaking and ability to understand multidimensional questionnaires,
  • Subjective tinnitus of peripheral origin (middle or inner ear auditory nerve)
  • Subjective tinnitus stable and chronic (lasting for more than 6 months)
  • Subjective tinnitus that can be characterized by tinnitus matching
  • Normal hearing or moderate hearing loss

Exclusion Criteria

  • Fluctuating tinnitus,
  • Unilateral or bilateral severe or profound hearing loss,
  • Claustrophobia, visual, impairment, vertigo or dizziness, chronic headache or any other condition contraindicating virtual immersion
  • Psychiatric condition requiring immediate management
  • Pregnant or breastfeeding women
  • Protected adults (including individual under guardianship by court order)
  • Persons deprived of their liberty by judicial or administrative decision

Outcomes

Primary Outcomes

Subjective Tinnitus Severity Scale (S.T.S.S.)

Time Frame: 5 months

16 items multidimensional questionnaire (validated in French) Score 0 to 16 (maximum severity)

Secondary Outcomes

  • Tinnitus Handicap Questionnaire (THI)(5 months)
  • Visual Analog Scale Tinnitus Loudness(5 months)
  • Hospital Anxiety Depression Scale(5 months)
  • Visual Analog Scale Tinnitus Intrusiveness(5 months)

Study Sites (1)

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