- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00748475
Countering Stimulus-Induced Alpha-Desynchronization to Treat Tinnitus
February 19, 2013 updated by: Nathan Weisz, University of Konstanz
The purpose of the study is to examine the effect of alpha-neurofeedback while subjects listen to a noise on tinnitus.
Study Overview
Study Type
Interventional
Enrollment (Actual)
12
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 70 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Duration of Tinnitus >= 6 months and <= 20 years
- Subjective Tinnitus
Exclusion Criteria:
- History of neurological or more than mild psychiatric diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: NON_RANDOMIZED
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Neurofeedback
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Reduction of tinnitus distress using the Tinnitus Questionaire
Time Frame: Before the first and after the last session.
|
Before the first and after the last session.
|
Cortical Alpha Power
Time Frame: Before the first and after the last session
|
Before the first and after the last session
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nathan Weisz, PhD, University Konstanz
- Study Chair: Thomas Hartmann, Dipl.-Psych., University Konstanz
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2008
Primary Completion (ACTUAL)
May 1, 2010
Study Registration Dates
First Submitted
September 5, 2008
First Submitted That Met QC Criteria
September 5, 2008
First Posted (ESTIMATE)
September 8, 2008
Study Record Updates
Last Update Posted (ESTIMATE)
February 20, 2013
Last Update Submitted That Met QC Criteria
February 19, 2013
Last Verified
February 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TE0602-1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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