Exploration of Cortical Neural Network in Patients With Bothersome Tinnitus

Tinnitus Clinical Trial

Official title:

Exploration of Cortical Neural Network in Patients With Bothersome Tinnitus

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01385540
• Other study ID #: 201106289
• Status: Terminated
• Phase: N/A
• First received: June 28, 2011
• Last updated: February 29, 2012
• Start date: July 2011
• Est. completion date: August 2011

Study information

• Verified date: February 2012
• Source: Washington University School of Medicine
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

This will be an experimental task-based functional MRI pilot study involving the neuroimaging assessment of patients with severely bothersome tinnitus, defined by a global bothersome scale. The investigators plan to enroll a total of 12 participants (6 severely bothered tinnitus and 6 age-matched non-tinnitus controls) over the course of six months to undergo task-based imaging. Subjects in the tinnitus group may have previously participated in the CTRWU study (HRPO: 07-0689) conducted by Dr. Jay Piccirillo at Washington University and have given permission to be contacted for consideration in future studies. The selected paradigm will allow us to advance knowledge about the role of the attention, control, and other cortical networks in the development and maintenance of bothersome tinnitus.

Description:

Task-Based Functional Magnetic Resonance Imaging (fMRI) The task-based fMRI protocol is based on work performed at Washington University by Dr. Gordon Shulman and published in The Journal of Neuroscience.(Shulman, Astafiev, Franke, Pope, Snyder, McAvoy, and Corbetta 2009) Individuals will be shown a target, which is randomly selected from 12 objects designated as targets, before each scan. The target for a scan will never appear as a non-target object in another scan. Per established protocol, individuals will fixate on a central cross prior to imaging. Individuals will press a MR-compatible button when they detect the target. Target objects only appear in the cued stream. Cues, a filled red square, are programmed to occur, on average, every 2.06, 4.12, or 6.18 seconds within a temporal window of ± 400 milliseconds centered on those values.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 7
• Est. completion date: August 2011
• Est. primary completion date: August 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Men and women between the ages of 18 to 60 years

• Subjective, unilateral or bilateral, non-pulsatile tinnitus of 6 month's duration or greater

• Either "moderately bothered" or "severely bothered" on the Global Bothersome scale

• THI score of = 30.

• Able to give written informed consent

• Able to read, write, speak and understand English fluently

Exclusion Criteria:

• Tinnitus related to cochlear implantation, retrocochlear lesion, or other known anatomic lesions of the ear and temporal bone

• History of Ménière's Disease

• History of hyperacusis or misophonia (hyper-sensitivity to noises)

• Cardiac pacemakers, intracardiac lines, implanted medication pumps, implanted electrodes in the brain, or any other contraindication for MRI scan

• An acute or chronic unstable medical condition which, in the opinion of the investigator, would require stabilization prior to testing.

• Any active ear disease that, in the opinion of the PI or mentor, needs to be further evaluated

• A Short Blessed Test score of 9 or greater

• PHQ-9 score = 10; consistent with diagnosis of moderate depression.

• History of seizure disorder or other neurological condition.

• Any psychiatric co-morbidity that may complicate the interpretation of study results. Subjects may not be currently taking antidepressants.

• Any tinnitus related to a Workman's Compensation claim or litigation-related event

• Currently pregnant: Women of childbearing potential must have a negative urine pregnancy test prior to MRI

• Weight over 300 pounds

• History of claustrophobia

• Inability to lay flat for 2 hours

• Active alcohol and/or drug dependence or history of alcohol and/or drug dependence within the last year

• Any medical condition that, in the opinion of the investigators, confounds study results or places the subject at greater risk

• Unable to provide written informed consent

• Blindness or inability to see screen for task-based testing without eyeglasses, subjects may wear contacts if able to lie flat and keep eyes focused on testing screen for up to 2 hours.

• Previous participation in a task-based MRI study

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

• Tinnitus

Intervention

Behavioral:
• Task-Based Functional Magnetic Resonance Imaging (fMRI)
Individuals will be shown a target, which is randomly selected from 12 objects designated as targets, before each scan. The target for a scan will never appear as a non-target object in another scan. Per established protocol, individuals will fixate on a central cross prior to imaging. Individuals will press a MR-compatible button when they detect the target. Target objects only appear in the cued stream. Cues, a filled red square, are programmed to occur, on average, every 2.06, 4.12, or 6.18 seconds within a temporal window of ± 400 milliseconds centered on those values.

Locations

Country	Name	City	State
United States	Washington University School of Medicine	St. Louis	Missouri

Sponsors (2)

Lead Sponsor	Collaborator
Washington University School of Medicine	American Tinnitus Association

Country where clinical trial is conducted

United States,