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Transcranial Electrical and Acoustic Stimulation for Tinnitus (tEAS)

Primary Purpose

Tinnitus, Tinnitus, Subjective

Status
Recruiting
Phase
Not Applicable
Locations
Switzerland
Study Type
Interventional
Intervention
transcranial Random Noise Stimulation (tRNS) with acoustic stimulation (AS)
transcranial Random Noise Stimulation (tRNS) without acoustic stimulation (AS)
Sponsored by
University of Zurich
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tinnitus

Eligibility Criteria

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

Inclusion Criteria:

  • Male and female patients 18 years to 75 years of age
  • Persistent chronic tinnitus with duration of more than 3 months
  • Signed Informed Consent after being informed about the study
  • Fluent in German
  • Tinnitus with a THI Grade 2 to 4 (18-76 points)
  • Willing and able to attend the study visits

Exclusion Criteria:

  • Actual neurological or psychiatric disorders
  • Hyperacusis
  • Regular intake of medication influencing the central nervous system (e.g. neuroleptics, hypnotics, sedatives, and anti-epileptics)
  • Implanted pacemaker
  • Surgical implants in the head region, such as cochlea implants
  • Asymmetrical hearing (more than 20dB side difference), pantonal hearing loss > 40dB in any measured frequency up to 2kHz
  • Women who are pregnant or breast feeding
  • Intention to become pregnant during the course of the study
  • Known or suspected non-compliance, drug or alcohol abuse
  • Participation in another study with investigational drug within the 30 days preceding and during the present study,
  • Enrolment of the investigator, his/her family members, employees and other dependent persons

Sites / Locations

  • University Hospital Zurich, University ZurichRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Study Intervention(s) A

Study Intervention(s) B = Control Intervention

Arm Description

TRNS bilateral temporal regions combined with AS for 20 minutes Sham-tRNS bilateral temporal regions combined with Sham-AS for 20 minutes

TRNS bilateral temporal regions for 20 minutes Sham-tRNS bilateral temporal regions for 20 minutes

Outcomes

Primary Outcome Measures

Change of self-report Visual Analogue Scale (VAS) ratings on tinnitus severity (loudness, distress)
Minmum value = 1, maximum value =10. The higher scores means a worse outcome.
Change of minimum masking level (MML)

Secondary Outcome Measures

event-related EEG power in alpha band
The influence of simultaneous tRNS and AS stimulation on neurophysiology will be investigated as a secondary outcome. Resting state and event-related EEG (auditory oddball) (Attias et al., 1993) will be recorded for that purpose.

Full Information

First Posted
August 9, 2020
Last Updated
November 21, 2022
Sponsor
University of Zurich
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1. Study Identification

Unique Protocol Identification Number
NCT04551404
Brief Title
Transcranial Electrical and Acoustic Stimulation for Tinnitus
Acronym
tEAS
Official Title
Transcranial Electrical and Acoustic Stimulation for Tinnitus: A Randomized Double Blind Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
December 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Zurich

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
Transcranial electrical stimulation (tES) is an umbrella term for non-invasive brain stimulation using weak currents. It comprises transcranial direct current stimulation (tDCS), which is the most established and used method applying constant direct current, transcranial alternating current stimulation (tACS) with sinusoidal current in a fixed frequency, and finally transcranial random noise stimulation (tRNS), which is a subform of tACS generating a random range of low and high frequency alternating currents. A pilot study conducted by Shekhawat and colleagues in 2015 tested the effects of simultaneous electrical and acoustic stimulation. Using tDCS and bilateral broadband noise simultaneously, they found that more tinnitus patients report an improvement in tinnitus perception in comparison to conditions only using tDCS or sham. Further similar approaches very published in recent years, namely a pilot study conducted by Teissmann et al in 2014; study protocols of Rabau et al. in 2015 and Shekhawat et al. in 2015; and an experimental study by Lee et al. in 2017. Results were indicative of a superior efficacy of combined electrical and acoustic approaches, while large-scale controlled studies have not been performed. The need for extension and replication of these approaches is therefore timely. The aim behind our proposed approach, similar to the bimodal approaches above, is to couple the effects of tRNS and acoustic stimulation (AS) for better temporary tinnitus suppression and possible reversal of maladaptive neuroplasticity related to tinnitus. We aim at targeting the (bilateral) auditory cortex with tRNS as in former studies and combine it with white noise (WN) stimulation. This specific combination is novel in its nature and is building on cortical excitability following tRNS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tinnitus, Tinnitus, Subjective

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
The crossover within-person design with 2 groups, 2 active conditions and appropriate control/pseudo-placebo/sham session is double-blinded. Overall, participants will undergo 20 stimulation visits and 6 additional assessment visits. Prior to conducting the above study, a pilot study of 40 patients and just 6 visits will be conducted to validate clinical procedures and outcomes. This procedure was approved by the ethics committee.
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Study Intervention(s) A
Arm Type
Experimental
Arm Description
TRNS bilateral temporal regions combined with AS for 20 minutes Sham-tRNS bilateral temporal regions combined with Sham-AS for 20 minutes
Arm Title
Study Intervention(s) B = Control Intervention
Arm Type
Experimental
Arm Description
TRNS bilateral temporal regions for 20 minutes Sham-tRNS bilateral temporal regions for 20 minutes
Intervention Type
Other
Intervention Name(s)
transcranial Random Noise Stimulation (tRNS) with acoustic stimulation (AS)
Intervention Description
The study intervention consists of a bilateral tRNS application over temporal regions, parallel to the application of AS with WN 15 dB above the individual MML in one study arm. TRNS will be applied using two electrodes (35 qcm, 0,9% saline -soaked). Stimulus intensity will be below individual sensation threshold, but max. 2 mA. AS will never surpass 85 dB SPL at the ears.
Intervention Type
Other
Intervention Name(s)
transcranial Random Noise Stimulation (tRNS) without acoustic stimulation (AS)
Intervention Description
The study intervention consists of a bilateral tRNS application over temporal regions
Primary Outcome Measure Information:
Title
Change of self-report Visual Analogue Scale (VAS) ratings on tinnitus severity (loudness, distress)
Description
Minmum value = 1, maximum value =10. The higher scores means a worse outcome.
Time Frame
up to 6 months
Title
Change of minimum masking level (MML)
Time Frame
up to 6 months
Secondary Outcome Measure Information:
Title
event-related EEG power in alpha band
Description
The influence of simultaneous tRNS and AS stimulation on neurophysiology will be investigated as a secondary outcome. Resting state and event-related EEG (auditory oddball) (Attias et al., 1993) will be recorded for that purpose.
Time Frame
up to 6 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: Male and female patients 18 years to 75 years of age Persistent chronic tinnitus with duration of more than 3 months Signed Informed Consent after being informed about the study Fluent in German Tinnitus with a THI Grade 2 to 4 (18-76 points) Willing and able to attend the study visits Exclusion Criteria: Actual neurological or psychiatric disorders Hyperacusis Regular intake of medication influencing the central nervous system (e.g. neuroleptics, hypnotics, sedatives, and anti-epileptics) Implanted pacemaker Surgical implants in the head region, such as cochlea implants Asymmetrical hearing (more than 20dB side difference), pantonal hearing loss > 40dB in any measured frequency up to 2kHz Women who are pregnant or breast feeding Intention to become pregnant during the course of the study Known or suspected non-compliance, drug or alcohol abuse Participation in another study with investigational drug within the 30 days preceding and during the present study, Enrolment of the investigator, his/her family members, employees and other dependent persons
Facility Information:
Facility Name
University Hospital Zurich, University Zurich
City
Zurich
ZIP/Postal Code
8091
Country
Switzerland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicole Peter, MD
Phone
+41432538826
Email
nicole.peter-siegrist@usz.ch
First Name & Middle Initial & Last Name & Degree
Tobias Kleinjung, Prof.
Phone
+41432539146
Email
tobias.kleinjung@usz.ch

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
27242932
Citation
Antal A, Herrmann CS. Transcranial Alternating Current and Random Noise Stimulation: Possible Mechanisms. Neural Plast. 2016;2016:3616807. doi: 10.1155/2016/3616807. Epub 2016 May 3.
Results Reference
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PubMed Identifier
25587455
Citation
Claes L, Stamberger H, Van de Heyning P, De Ridder D, Vanneste S. Auditory cortex tACS and tRNS for tinnitus: single versus multiple sessions. Neural Plast. 2014;2014:436713. doi: 10.1155/2014/436713. Epub 2014 Dec 22.
Results Reference
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PubMed Identifier
25694243
Citation
Joos K, De Ridder D, Vanneste S. The differential effect of low- versus high-frequency random noise stimulation in the treatment of tinnitus. Exp Brain Res. 2015 May;233(5):1433-40. doi: 10.1007/s00221-015-4217-9. Epub 2015 Feb 19.
Results Reference
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PubMed Identifier
31439873
Citation
Kreuzer PM, Poeppl TB, Rupprecht R, Vielsmeier V, Lehner A, Langguth B, Schecklmann M. Daily high-frequency transcranial random noise stimulation of bilateral temporal cortex in chronic tinnitus - a pilot study. Sci Rep. 2019 Aug 22;9(1):12274. doi: 10.1038/s41598-019-48686-0.
Results Reference
background
PubMed Identifier
28417104
Citation
Lee HY, Choi MS, Chang DS, Cho CS. Combined Bifrontal Transcranial Direct Current Stimulation and Tailor-Made Notched Music Training in Chronic Tinnitus. J Audiol Otol. 2017 Apr;21(1):22-27. doi: 10.7874/jao.2017.21.1.22. Epub 2017 Mar 30.
Results Reference
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PubMed Identifier
29730252
Citation
Mohsen S, Mahmoudian S, Talebian S, Pourbakht A. Prefrontal and auditory tRNS in sequence for treating chronic tinnitus: a modified multisite protocol. Brain Stimul. 2018 Sep-Oct;11(5):1177-1179. doi: 10.1016/j.brs.2018.04.018. Epub 2018 Apr 25. No abstract available.
Results Reference
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PubMed Identifier
26554670
Citation
Rabau S, Van Rompaey V, Van de Heyning P. The effect of Transcranial Direct Current Stimulation in addition to Tinnitus Retraining Therapy for treatment of chronic tinnitus patients: a study protocol for a double-blind controlled randomised trial. Trials. 2015 Nov 10;16:514. doi: 10.1186/s13063-015-1041-2.
Results Reference
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PubMed Identifier
25285987
Citation
Shekhawat GS, Kobayashi K, Searchfield GD. Methodology for studying the transient effects of transcranial direct current stimulation combined with auditory residual inhibition on tinnitus. J Neurosci Methods. 2015 Jan 15;239:28-33. doi: 10.1016/j.jneumeth.2014.09.025. Epub 2014 Oct 5.
Results Reference
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PubMed Identifier
24587113
Citation
Teismann H, Wollbrink A, Okamoto H, Schlaug G, Rudack C, Pantev C. Combining transcranial direct current stimulation and tailor-made notched music training to decrease tinnitus-related distress--a pilot study. PLoS One. 2014 Feb 25;9(2):e89904. doi: 10.1371/journal.pone.0089904. eCollection 2014.
Results Reference
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PubMed Identifier
25245591
Citation
Van Doren J, Langguth B, Schecklmann M. Electroencephalographic effects of transcranial random noise stimulation in the auditory cortex. Brain Stimul. 2014 Nov-Dec;7(6):807-12. doi: 10.1016/j.brs.2014.08.007. Epub 2014 Aug 26.
Results Reference
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PubMed Identifier
24391599
Citation
Vanneste S, Fregni F, De Ridder D. Head-to-Head Comparison of Transcranial Random Noise Stimulation, Transcranial AC Stimulation, and Transcranial DC Stimulation for Tinnitus. Front Psychiatry. 2013 Dec 18;4:158. doi: 10.3389/fpsyt.2013.00158. eCollection 2013.
Results Reference
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PubMed Identifier
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Citation
Martins ML, Kleinjung T, Meyer M, Raveenthiran V, Wellauer Z, Peter N, Neff P. Transcranial electric and acoustic stimulation for tinnitus: study protocol for a randomized double-blind controlled trial assessing the influence of combined transcranial random noise and acoustic stimulation on tinnitus loudness and distress. Trials. 2022 May 19;23(1):418. doi: 10.1186/s13063-022-06253-5.
Results Reference
derived

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Transcranial Electrical and Acoustic Stimulation for Tinnitus

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