Physiological Regulation of Chronic Tinnitus

Tinnitus Clinical Trial

— NeuroTin  

Official title:

Physiological Regulation of Chronic Tinnitus

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05737888
• Other study ID #: NeuroTin
• Status: Completed
• Phase: N/A
• Start date: February 14, 2017
• Est. completion date: March 30, 2023

Study information

• Verified date: November 2023
• Source: Wyss Center for Bio and Neuroengineering
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The present project involves research on humans with the aim to characterize the reduction of chronic, continuous, non-pulsatile and debilitating tinnitus in humans by comparing neurofeedback (fMRI or EEG) to the current gold standard behavioral cognitive therapy.

Description:

Chronic tinnitus is affecting 10-15% of people typically for many decades, with increasing prevalence with aging. Multiple therapy forms for tinnitus exist (including cognitive behavioral therapy, external white noise stimulation, meditation, and various kinds of alternative approaches), but up to now, no generally accepted successful treatment exists. Previously, it was shown that voluntary control of the activation of the auditory cortex can be learned by means of real-time functional Magnetic Resonance Imaging (fMRI) neurofeedback, and that it may alleviate tinnitus symptoms. The same seems to hold for learned increase of alpha activity localized in the auditory cortex through electroencephalography (EEG) neurofeedback. Given the high prevalence of chronic tinnitus, its significant burden for affected individuals, and given the absence of generally effective therapy, neurofeedback training for tinnitus has the potential to become a clinical application.

The main goal of this project is to comparatively assess tinnitus reduction using neurofeedback (fMRI or EEG) compared to cognitive behavioral therapy in participants with chronic severe tinnitus.

• The participants are assigned to 3 different experimental groups (EEG neurofeedback, fMRI neurofeedback, or cognitive behavioral therapy). The participation per subject will last from 4 to 12 months.

• The participants undergo medical tests including audiological tests as well as questionnaires related to tinnitus and quality of life at different timepoints of the study (pre and post training visits).

• At the end of the experimental visits, each participant will have one early and one late post-assessment evaluation visits.

• In order to evaluate the longer-term evolution of tinnitus over time, long-term follow-ups will be scheduled starting at 9 months after the final experimental visit, and will occur every 4.5 months thereafter, until research ends (for a maximum of 5 years).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 85
• Est. completion date: March 30, 2023
• Est. primary completion date: December 6, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Age between 18 to 80 years

2. Tinnitus Handicap Inventory = 48

3. Chronic, persistent, non-pulsatile tinnitus for minimum 6 months

4. Functional hearing

5. Normal inner ear structure assessment using an ear microscope, normal tympanic membrane mobility

6. Participant willing, able and available to participate in the entire research, including completion of questionnaires and traveling to research sites for the duration of the trial

Exclusion Criteria:

1. Contraindication to MRI (e.g. non compatible cochlear implant, pacemaker, deep brain stimulation)

2. Conductive hearing loss exceeding 20 dB at two or more frequencies

3. Known diagnoses causing tinnitus or hearing loss:

• Known systemic disease (vestibular schwannoma, endolymphatic hydrops)

• Lesion in central nervous system, including history of severe cranio-cerebral trauma

• Acute ear canal or middle ear inflammation or effusion

4. Significant neurologic disease, psychiatric disease, substance abuse or acute allergic disease

5. Ongoing medication that is known to treat, influence, or cause tinnitus (e.g. high-dose aspirin, quinidine, aminoglycosides)

6. Ongoing or recent (completed since less than 4 weeks) tinnitus therapy (e.g. tinnitus maskers, acupuncture)

7. Participation in competitive or pharmacological study

8. Pregnant woman

Related Conditions & MeSH terms

• Tinnitus

Intervention

Other:
• fMRI Neurofeedback
15 intervention sessions on a 3T MRI scanner.
• EEG Neurofeedback
15 intervention sessions with a standard EEG-cap with 64 active electrodes.

Behavioral:
• Cognitive Behavioral Therapy
10 intervention sessions of CBT group therapy, as per local university hospital standard of care.

Locations

Country	Name	City	State
Switzerland	Dept. of Otology, Audiology and Cochlear Implant Surgery, University Hospital Geneva	Geneva	GE

Sponsors (2)

Lead Sponsor	Collaborator
Wyss Center for Bio and Neuroengineering	Ecole Polytechnique Fédérale de Lausanne

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Behavioral improvement of tinnitus as measured by the Tinnitus Handicap Inventory (THI)	To show that behavioral improvement of tinnitus after intensive neurofeedback training is equivalent or better than improvement obtained after attending group cognitive behavioral therapy, as measured by Tinnitus Handicap Inventory (THI) scores reported before experiment and at late post-assessment (significant difference, p-value < 0.05). THI ranges from low scores (grade 1 - slight or no handicap), to highest scores (grade 5 - catastrophic handicap).	8 months
Secondary	Audiological measures	If reported tinnitus scores correlate with audiological measures during research for each experimental group;	8 months
Secondary	Training effect	If significant behavioral change as shown by a THI grade reduction is observed before/after experiment in each group;	8 months
Secondary	Other factors	If there are external parameters influencing reported tinnitus levels for each group during the research, based on participant questionnaires (i.e., placebo effect of the trainer/CBT professional provider, motivation levels);	8 months
Secondary	Correlation with BOLD signal	Specifically for group 1 - fMRI neurofeedback, whether evolution of audiological and tinnitus measures at different research timepoints correlate with BOLD signal of the auditory cortex;	8 months
Secondary	Correlation with alpha activity	Specifically for group 2 - EEG neurofeedback, whether evolution of audiological and tinnitus measures at different research timepoints correlate with alpha activity of the auditory cortex;	8 months
Secondary	Acceptance of intensive schedule	Specifically for group 1 and 2, acceptance of neurofeedback intensive schedule of visits by participants.	8 months