- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05667168
Physiotherapeutic Approach to Tinnitus
Physiotherapeutic Diagnostic and Therapy of Tinnitus
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Clients will be divided into individual (8) therapy groups. The proband groups formed will be treated by individual researchers according to a similar methodology, each with a different therapeutic intervention for tinnitus. The main dominant variables to be monitored will be tinnitus intensity assessed on a visual numerical scale from 0-10, and quality of life observed using different questionnaires (which questionnaires will be used will be addressed in the course of the research, as this is not standardly used for tinnitus in the Czech region). The questionnaires will measure the quality of life and intensity of tinnitus of probands at the beginning and the end of the experiment, regardless of their racial, political, social, religious, and philosophical views and classification. Sexual orientation and criminal offences will not be questioned or addressed. As part of the questionnaires, clients will be subjected to musculoskeletal diagnosis by kinesiological analysis and tinnitus diagnosis by examination and will be further assigned to appropriate therapy sections (8). The questionnaires will be given to probands in hard copy at the initial assessment, during which the proband will complete and submit the questionnaire. The exit questionnaire will be administered similarly at the exit examination, i.e. the proband's last visit to the research team.
The selected therapeutic interventions in each section will be a low-power laser, high-power laser, radiofrequency therapy, manual therapy of the temporomandibular joint, manual treatment of the cervical and adjacent thoracic spine, myofascial chain work in the context of closed and open kinematic patterns, psychological guidance mediated by a psychosomatic physician, and addressing healthy lifestyle issues. The therapy will take place 2-3 times a week; the therapeutic unit will be 45 min and will be oriented to one therapeutic approach from the above list. The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week). The therapy will take place at the clinical workplace of private practice (anonymise) and the practice rooms of the Department of Physiotherapy Faculty of Physiotherapy of Charles University. At the end of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Praha, Czechia
- Charles University, Faculty of physical education and sport
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- neurologically diagnosed tinnitus
- age 20-80 years
- tinnitus of any nature persisting for more than 3 months
Exclusion Criteria:
- acute or chronic medical conditions requiring medication
- history of head and cervical spine trauma
- oncologic therapy
- psychological or psychiatric treatment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: High power laser
The application of high-intensity laser on cervical muscles, 50J/cm2, 980nm, 0 Hz, on processus mastoideus and porus acusticus externus. Administration of tinnitus intensity on scale 0-10 and questionary. |
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
Experimental: Low power laser
The application of low-intensity laser on cervical muscles, 4J/cm2, 980nm, 0 Hz, on processus mastoideus and porus acusticus externus.
Administration of tinnitus intensity on scale 0-10 and questionary.
|
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
Experimental: Radio-frequention therapy
Applying radio-frequentation current on cervical muscles, 10-50% of intensity, 0 Hz.
Administration of tinnitus intensity on a scale of 0-10 and questionary.
|
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
Experimental: Manual therapy of temporomandibular joint,.
A manual physiotherapeutic approach to the temporomandibular joint will treat participants.
Administration of tinnitus intensity on a scale of 0-10 and questionary.
|
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
Experimental: Manual therapy of the cervical spine.
A manual physiotherapeutic approach to the cervical spine will treat participants.
Administration of tinnitus intensity on a scale of 0-10 and questionary.
|
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
Active Comparator: Physical exercising.
Participants will be treated by physical exercising in closing and opening muscle chains.
Administration of tinnitus intensity on a scale of 0-10 and questionary.
|
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
Active Comparator: Cognitive therapy
Participants will be treated with cognitive therapy by a psychologist.
Administration of tinnitus intensity on a scale of 0-10 and questionary.
|
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
Placebo Comparator: Life style.
Participants will be treated only by modulation of their lifestyle.
Administration of tinnitus intensity on a scale of 0-10 and questionary.
|
The therapy will take place 2-3 times a week; the therapeutic unit will last 45 minutes and will be oriented towards one therapeutic approach from the above list.
The total number of therapy sessions will be limited to 3 months (i.e. three months, 2-3 times a week).
After completion of the 3-month therapy, a follow-up examination will be performed again by kinesiological analysis, questions about the intensity of tinnitus according to a numerical scale and quality of life by a selected questionnaire.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Decreasing of sensoric feeling of tinnitus.
Time Frame: 3 month
|
Due to analog numeric scale (0-10 where 0 mean without tinnitus and 10 maximum intensity of tinnitus), will be find the most effective approach to decreasing hearable sound typical for tinnitus.
|
3 month
|
Changing of life quality due to tinnitus.
Time Frame: 3 month
|
According to the questionnaire survey (THI) the effect of the treatment will be shown.
|
3 month
|
Collaborators and Investigators
Investigators
- Study Director: Jitka Malá, PhD., Charles University Prague, Czech Republic
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FTVS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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