- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06360731
The Effect of 4-7-8 Breathing Exercise Technique on Tinnitus
The Effect of 4-7-8 Breathing Exercise Technique on Tinnitus Handicap, Psychological Factors, and Sleep Quality in Tinnitus Patients: A Randomized Controlled Study
The goal of this study is to evaluate the effect of 4-7-8 breathing exercise on tinnitus handicap, psychological factors and sleep quality.
There will be a parallel-group randomized controlled trial study and consists of two groups.
Both groups will receive 1 hour of informative session on tinnitus and the experimental group will also perform 4-7-8 breathing exercises for 6 weeks. Visual analog scale, tinnitus handicap inventory, insomnia severity index, trait anxiety inventory, and perceived stress scale will be applied before and after the application.
Study Overview
Status
Conditions
Detailed Description
The aim of this study is to evaluate the effect of 4-7-8 breathing exercise technique on tinnitus handicap, psychological factors and sleep quality. It is also aimed to compare the results of the experimental group and those who received only 1 hour of informative session on tinnitus (Control group).
The study will employ a parallel-group randomized controlled trial design. Both groups will receive 1 hour of informative session on tinnitus and the experimental group will also perform 4-7-8 breathing exercises for 6 weeks.
Visual analog scale, tinnitus handicap inventory, insomnia severity index, trait anxiety inventory,and perceived stress scale will be applied to all patients before and after the application.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Ankara, Turkey
- Gokce Saygi Uysal
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Izmir, Turkey
- Audiology Unit of the Department of Otorhinolaryngology, Ege University Faculty of Medicine Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged between 18-65 years with subjective idiopathic tinnitus complaints for at least six months
- Must be able to speak and read Turkish
- Must be able to answer the questionnaire questions and perform the 4-7-8 breathing exercises regularly
Exclusion Criteria:
- Any neuro-otologic, psychiatric, neurologic, or cognitive problems, objective tinnitus, chronic medication use, asthma diagnosis or respiratory distress
- Receivement of any tinnitus treatment or tinnitus informative session actively
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Experimental Group
Experimental group who consists of subjective tinnitus patients will receive 1 hour of informative session on tinnitus and also perform 4-7-8 breathing exercises for 6 weeks
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Participants in experimental group will be individually provided with informative session on tinnitus for one hour by researchers.
During the informative session, the participants will be given general information about tinnitus and will be informed about the possible causes, symptoms, diagnosis, therapy, or treatment processes, and coping methods.
The participants will be also given a printed informative brochure on tinnitus.
In the same session, after one hour of informative session, the 4-7-8 breathing exercise method will be demonstrated by the same researchers.
In addition, a video showing how to perform the 4-7-8 breathing exercise technique will be sent as a text message to their cell phones.
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Active Comparator: Control Group
Control group who consists of subjective tinnitus patients will receive 1 hour of informative session on tinnitus only
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Participants in control group will be individually provided with informative session on tinnitus only for one hour by researchers G.K. and G.S.U. from both clinics.
During the informative session, the participants will be given general information about tinnitus and inform about the possible causes, symptoms, diagnosis, therapy, or treatment processes, and coping methods.
The participants will be also given a printed informative brochure on tinnitus.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Visual Analog Scale (VAS)
Time Frame: Baseline
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Patients will be asked to assess the degree of distress and annoyance associated with their tinnitus, as well as its severity, using a Visual Analog Scale (VAS) from 0 to 10 both before and after the application.
An increase in these areas is shown by an increase in the score.
Minimum score value is 0 and maximum value is 10.
All patients will be assessed before application.
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Baseline
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Visual Analog Scale (VAS)
Time Frame: Six weeks after baseline evaluation
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Patients will be asked to assess the degree of distress and annoyance associated with their tinnitus, as well as its severity, using a Visual Analog Scale (VAS) from 0 to 10 both before and after the application.
An increase in these areas is shown by an increase in the score.
Minimum score value is 0 and maximum value is 10.
All patients will be assessed six weeks after baseline evaluation.
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Six weeks after baseline evaluation
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Tinnitus Handicap Inventory (THI)
Time Frame: Baseline
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The Tinnitus Handicap Inventory (THI) assesses the catastrophic, emotional, and functional impacts of tinnitus and measures its effects on patients' daily functioning.
The THI consists of 25 items.
In the inventory, there are 25 items consisting of three options as 'yes', 'no', and 'sometimes'.
A 'yes' answer is worth 4 points and a 'no' answer is worth 0 points.
A maximum score of 100 points can be obtained from the THI.
The higher the score, the greater the perception of the tinnitus as a handicap.
Minimum score value is 0 and maximum value is 100.
All patients will be assessed before application.
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Baseline
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Tinnitus Handicap Inventory (THI)
Time Frame: Six weeks after baseline evaluation
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The Tinnitus Handicap Inventory (THI) assesses the catastrophic, emotional, and functional impacts of tinnitus and measures its effects on patients' daily functioning.
The THI consists of 25 items.
In the inventory, there are 25 items consisting of three options as 'yes', 'no', and 'sometimes'.
A 'yes' answer is worth 4 points and a 'no' answer is worth 0 points.
A maximum score of 100 points can be obtained from the THI.
The higher the score, the greater the perception of the tinnitus as a handicap.
Minimum score value is 0 and maximum value is 100.
All patients will be assessed six weeks after baseline evaluation.
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Six weeks after baseline evaluation
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Insomnia severity index (ISI)
Time Frame: Baseline
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Sleep quality of the patients was assessed with the insomnia severity index (ISI).
It is a questionnaire that evaluates the difficulties experienced in transitioning to and maintaining sleep, the level of stress caused by sleep problems, and impairments in daily functions, and thus determines the level of insomnia.
It consists of 7 questions in total.
Higher score indicates more insomnia symptoms.
Minimum score value is 0 and maximum value is 28.
All patients will be assessed before application.
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Baseline
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Insomnia severity index (ISI)
Time Frame: Six weeks after baseline evaluation
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Sleep quality of the patients was assessed with the insomnia severity index (ISI).
It is a questionnaire that evaluates the difficulties experienced in transitioning to and maintaining sleep, the level of stress caused by sleep problems, and impairments in daily functions, and thus determines the level of insomnia.
It consists of 7 questions in total.
Higher score indicates more insomnia symptoms.
Minimum score value is 0 and maximum value is 28.
All patients will be assessed six weeks after baseline evaluation.
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Six weeks after baseline evaluation
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Perceived stress scale -10 (PSS-10)
Time Frame: Baseline
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The Perceived Stress Scale-10 (PSS-10) will be administered to assess the stress perceived by tinnitus patients.
It was developed to measure the extent to which situations in one's life are considered stressful.
It consists of 10 questions.
The scores of PSS-10 vary between 0 and 40.
Greater perceived stress is indicated by higher scores.
The scores of PSS-10 vary between 0 and 40.
All patients will be assessed before application.
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Baseline
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Perceived stress scale -10 (PSS-10)
Time Frame: Six weeks after baseline evaluation
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The Perceived Stress Scale-10 (PSS-10) will be administered to assess the stress perceived by tinnitus patients.
It was developed to measure the extent to which situations in one's life are considered stressful.
It consists of 10 questions.
The scores of PSS-10 vary between 0 and 40.
Greater perceived stress is indicated by higher scores.
The scores of PSS-10 vary between 0 and 40.
All patients will be assessed six weeks after baseline evaluation.
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Six weeks after baseline evaluation
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Trait Anxiety Scale (TAS)
Time Frame: Baseline
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The trait anxiety subscale of the State-Trait Anxiety Inventory was used to assess the level of anxiety in those with tinnitus.
The TAS is a 4-point Likert-type scale consisting of twenty items that aims to determine how the individual feels regardless of the situation and conditions in which they find themselves.
A score between 20 and 80 is obtained from this scale.
Higher scores indicate higher level of anxiety.
A score between 20 and 80 is obtained from this scale.
All patients will be assessed before application.
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Baseline
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Trait Anxiety Scale (TAS)
Time Frame: Six weeks after baseline evaluation
|
The trait anxiety subscale of the State-Trait Anxiety Inventory was used to assess the level of anxiety in those with tinnitus.
The TAS is a 4-point Likert-type scale consisting of twenty items that aims to determine how the individual feels regardless of the situation and conditions in which they find themselves.
A score between 20 and 80 is obtained from this scale.
Higher scores indicate higher level of anxiety.
A score between 20 and 80 is obtained from this scale.
All patients will be assessed six weeks after baseline evaluation.
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Six weeks after baseline evaluation
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Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Koksoy S, Eti CM, Karatas M, Vayisoglu Y. The Effects of Yoga in Patients Suffering from Subjective Tinnitus. Int Arch Otorhinolaryngol. 2018 Jan;22(1):9-13. doi: 10.1055/s-0037-1601415. Epub 2017 Apr 3.
- Vierra J, Boonla O, Prasertsri P. Effects of sleep deprivation and 4-7-8 breathing control on heart rate variability, blood pressure, blood glucose, and endothelial function in healthy young adults. Physiol Rep. 2022 Jul;10(13):e15389. doi: 10.14814/phy2.15389.
- Gilles A, Jacquemin L, Cardon E, Vanderveken OM, Joossen I, Vermeersch H, Vanhecke S, Van den Brande K, Michiels S, Van de Heyning P, Van Rompaey V. Long-term effects of a single psycho-educational session in chronic tinnitus patients. Eur Arch Otorhinolaryngol. 2022 Jul;279(7):3301-3307. doi: 10.1007/s00405-021-07026-7. Epub 2021 Oct 1.
- Apoorva HM, Jayaram M, Patil NJ. Usefulness of Yoga in the management of tinnitus during COVID-19: A narrative review. J Ayurveda Integr Med. 2024 Jan-Feb;15(1):100822. doi: 10.1016/j.jaim.2023.100822. Epub 2023 Dec 28.
- Ismail AMA, Ali SM, Ghuiba K, Elfahl AMA, Tolba AMN, Ghaleb HAM. Autonomic functions, tinnitus annoyance and loudness, and quality of life: Randomized-controlled responses to bee-humming (vibrational) respiratory training in tinnitus elderly. Complement Ther Clin Pract. 2022 Aug;48:101611. doi: 10.1016/j.ctcp.2022.101611. Epub 2022 Jun 3.
- Gunjawate DR, Ravi R. Effect of yoga and meditation on tinnitus: a systematic review. J Laryngol Otol. 2021 Apr;135(4):284-287. doi: 10.1017/S0022215121000566. Epub 2021 Mar 11.
- Video: breathing exercises: 4-7-8 breath [Internet]. 2014 Available from: https://www.drweil.com/videos-features/videos/breathing-exercises-4-7-8-breath/
- Aksoy S, Firat Y, Alpar R. The Tinnitus Handicap Inventory: a study of validity and reliability. Int Tinnitus J. 2007;13(2):94-8.
- Boysan M, Güleç M, Beşiroğlu L, et al. Psychometric properties of the Insomnia Severity Index in Turkish sample. Anadolu Psikiyatri Derg 2010;11:248-252.
- Eskin M, Harlak H, Demirkıran F. The adaptation of the perceived stress scale into turkish: a reliability and validity analysis. Neuropsych Investig 2013;51:132-140.
- Öner N, Lecompte A. Manual of state trait anxiety inventory. Istanbul: Boğaziçi University Print House; 1998.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- 1018
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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