search
Back to results

Virtual Reality and Subjective Tinnitus (ReVA2)

Primary Purpose

Tinnitus, Tinnitus, Subjective

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Virtual Reality
Standard treatment
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tinnitus focused on measuring Subjective tinnitus, Virtual Reality, Cognitive Behavioral Therapy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Hôpital européen Georges-Pompidou AP-HPRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Virtual reality treatment

Standard treatment

Arm Description

Virtual reality immersion with 3D audio and visual rendering (8 weekly sessions)

Counselling Relaxation techniques Sound enrichment

Outcomes

Primary Outcome Measures

Subjective Tinnitus Severity Scale (S.T.S.S.)
16 items multidimensional questionnaire (validated in French) Score 0 to 16 (maximum severity)

Secondary Outcome Measures

Tinnitus Handicap Questionnaire (THI)
25 items multidimensional questionnaire (validated in French) Score 0 to 100 (maximum handicap)
Hospital Anxiety Depression Scale
14 item questionnaire (validated in French) Score 0 to 21 (maximum anxiety) Score 0 to 21 (maximum depression)
Visual Analog Scale Tinnitus Loudness
Likert-Scale 0 to 10 (maximum loudness)
Visual Analog Scale Tinnitus Intrusiveness
Likert-Scale 0 to 10 (maximum intrusiveness)

Full Information

First Posted
July 31, 2021
Last Updated
April 14, 2023
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Institut de recherche et de coordination acoustique/musique, Institut National de la Santé Et de la Recherche Médicale, France, Immersive Therapy
search

1. Study Identification

Unique Protocol Identification Number
NCT04987502
Brief Title
Virtual Reality and Subjective Tinnitus
Acronym
ReVA2
Official Title
Virtual Reality and Subjective Tinnitus
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 7, 2022 (Actual)
Primary Completion Date
April 7, 2024 (Anticipated)
Study Completion Date
April 7, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
Institut de recherche et de coordination acoustique/musique, Institut National de la Santé Et de la Recherche Médicale, France, Immersive Therapy

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tinnitus, Tinnitus, Subjective
Keywords
Subjective tinnitus, Virtual Reality, Cognitive Behavioral Therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Virtual reality treatment
Arm Type
Experimental
Arm Description
Virtual reality immersion with 3D audio and visual rendering (8 weekly sessions)
Arm Title
Standard treatment
Arm Type
Active Comparator
Arm Description
Counselling Relaxation techniques Sound enrichment
Intervention Type
Other
Intervention Name(s)
Virtual Reality
Intervention Description
8 sessions of virtual reality with 3D audio and visual rendering
Intervention Type
Behavioral
Intervention Name(s)
Standard treatment
Intervention Description
counselling, relaxation techniques, sound enrichment
Primary Outcome Measure Information:
Title
Subjective Tinnitus Severity Scale (S.T.S.S.)
Description
16 items multidimensional questionnaire (validated in French) Score 0 to 16 (maximum severity)
Time Frame
5 months
Secondary Outcome Measure Information:
Title
Tinnitus Handicap Questionnaire (THI)
Description
25 items multidimensional questionnaire (validated in French) Score 0 to 100 (maximum handicap)
Time Frame
5 months
Title
Hospital Anxiety Depression Scale
Description
14 item questionnaire (validated in French) Score 0 to 21 (maximum anxiety) Score 0 to 21 (maximum depression)
Time Frame
5 months
Title
Visual Analog Scale Tinnitus Loudness
Description
Likert-Scale 0 to 10 (maximum loudness)
Time Frame
5 months
Title
Visual Analog Scale Tinnitus Intrusiveness
Description
Likert-Scale 0 to 10 (maximum intrusiveness)
Time Frame
5 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Natacha Nohilé
Phone
3356095982
Email
natacha.nohile@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alain Londero, MD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital européen Georges-Pompidou AP-HP
City
Paris
ZIP/Postal Code
75015
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alain Londero
Email
alain.londero@aphp.fr

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Individual participant data (IPD) that underlie results in publication could be shared. IPD detailed in the protocol of a planned metaanalysis could be shared
IPD Sharing Time Frame
Two years after the last publication
IPD Sharing Access Criteria
Data sharing must be accepted by the sponsor and the PI based on a scientific project and scientific involvement of the PI team. Collaboration will be fostered. Data sharing must respect the agreements made with funders. Teams wishing obtain IPD must meet the sponsor and IP team to present scientific (and commercial) purpose, IPD needed, format of data transmission, and timeframe. Technical feasibility and financial support will be discussed before mandatory contractual agreement. Processing of shared data must comply with European General Data Protection Regulation (GDPR).
Citations:
PubMed Identifier
26773752
Citation
Malinvaud D, Londero A, Niarra R, Peignard P, Warusfel O, Viaud-Delmon I, Chatellier G, Bonfils P. Auditory and visual 3D virtual reality therapy as a new treatment for chronic subjective tinnitus: Results of a randomized controlled trial. Hear Res. 2016 Mar;333:127-135. doi: 10.1016/j.heares.2015.12.023. Epub 2016 Jan 8.
Results Reference
background

Learn more about this trial

Virtual Reality and Subjective Tinnitus

We'll reach out to this number within 24 hrs