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Different Stimuli Were Given to Patients With Chronic Pure Tone Tinnitus to Verify the Effective Treatment of Tinnitus.

Effects of Sound Stimulation, Somatosensory Stimulation, Vestibular Stimulation and the Combinations on Tinnitus Loudness and Tinnitus Related Distress in Patients

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04118907
Enrollment
120
Registered
2019-10-08
Start date
2020-06-30
Completion date
2020-10-30
Last updated
2020-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acoustic Stimulation, Somatic Stimulation, Tinnitus, Vestibular Stimulation

Keywords

tinnitus, stimulation

Brief summary

In this experiment, patients with chronic pure tone tinnitus were divided into three groups to receive auditory stimulation, somatosensory stimulation, vestibular stimulation and combined stimulation, in order to find an effective way to treat tinnitus

Detailed description

120 patients with chronic pure tone tinnitus over 6 months were randomly divided into 6 groups, one group was given auditory stimulation, one group was given somatosensory stimulation, one group was given auditory stimulation + somatosensory stimulation, one group was given auditory stimulation + vestibular stimulation, the last group was given auditory stimulation + somatosensory stimulation + vestibular stimulation.

Interventions

DEVICEmultiple sensory stimulation

The patients were recruited to record their medical history, and the hearing level, tinnitus indicators, vestibular function and tinnitus disability indicators were tested. Then the patients were randomly divided into six groups. They received the corresponding stimulation 20 minutes a day, 5 days a week for 3 weeks. After the last stimulation, the above tests were repeated immediately, one week later and three months later.

Sponsors

Dan Su
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Pure tone tinnitus * Unilateral and bilateral * female and male * Tinnitus has a history of more than 6 months

Exclusion criteria

* Pulsatile tinnitus of blood vessel * Meniere's disease * Chronic headache * Neurological diseases (such as brain tumors) * Patients with mental / mental illness undergoing treatment * Pregnant women and patients with other untreatable diseases

Design outcomes

Primary

MeasureTime frameDescription
Electrical audiometry and acoustic impedanceThree months from the time the patient was selected to the end of the stimulusAssessment of hearing in patients
Tinnitus frequency and loudnessThree months from the time the patient was selected to the end of the stimulusDetection of tinnitus frequency and loudness in patients
Tinnitus disability scaleThree months from the time the patient was selected to the end of the stimulusTinnitus handicap inventory score was used to detect the degree of tinnitus.0-16 points without disability, 18-36 points with mild disability, 38-56 points with moderate disability and 58-100 points with severe disability. The 95% confidence interval is 20 points, that is, the difference between the two tests before and after the experiment is greater than or equal to 20 points.

Countries

China

Contacts

Primary ContactDan Su, master
sudan19966991@outlook.com+8615755149100
Backup ContactBusheng Tong, doctor
2871638103@qq.com+8613956040273

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026