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Combined Transcranial and Peripheral Muscle Magnetic Stimulation in Chronic Tinnitus

Combined Transcranial and Peripheral Muscle Magnetic Stimulation in Chronic Tinnitus

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02306447
Acronym
rpms-tinn
Enrollment
54
Registered
2014-12-03
Start date
2014-08-31
Completion date
2016-04-30
Last updated
2016-05-13

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

Conditions

Chronic Tinnitus

Brief summary

Magnetic stimulation of the brain (repetitive transcranial magnetic stimulation) and of neck muscles (repetitive peripheral muscle stimulation) is used to alter tinnitus-related cortical activity and neck muscles tension.

Detailed description

Chronic tinnitus is characterized by several comorbid disorders. One of them is neck and back pain. Here, we investigate the feasibility, safety and clinical efficacy of the combination of repetitive transcranial magnetic stimulation (rTMS) and peripheral muscle stimulation (rPMS) in chronic tinnitus in a pilot study. rTMS is considered to interact with neural tinnitus networks. rPMS is suggested to bring relief to muscle tension. This is an one arm study where explorative analyses will be done with special consideration on patients suffering from neck pain in the analysis.

Interventions

DEVICErPMS and rTMS

rPMS Stimulation of the neck muscles in five medial-lateral movements starting from the neck: left and right trapezius and deltoid muscle, trapezius and lattissimus dorsi muslce, and over the backbone. 20 stimuli per movement with 2s inter-train interval; four repetitions for each of the five movements; the first 20 trains with a frequency of 5Hz, the second 20 trains at 20Hz; stimulation at individual comfortable level (20-30% stimulator output); round coil. rTMS 20Hz stimulation with 2000 stimuli over the left dorso-lateral prefrontal cortex at 110% motor threshold; followed by 1Hz stimulation with 2000 stimuli over the left temporo-parietal cortex; stimulation intensity 110% motor threshold; butterfly coil. For stimulation we use MagPro X100 (Medtronic, Denmark).

Sponsors

University of Regensburg
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Diagnosis of bothersome, subjective chronic tinnitus * Duration of tinnitus more than 6 months

Exclusion criteria

* Objective tinnitus * Treatable cause of the tinnitus * Involvement in other treatments for tinnitus at the same time * Clinically relevant psychiatric comorbidity * Clinically relevant unstable internal or neurological comorbidity * History of or evidence of significant brain malformation or neoplasm, head injury * Cerebral vascular events * Neurodegenerative disorder affecting the brain or prior brain surgery * Metal objects in and around body that can not be removed * Pregnancy * Alcohol or drug abuse * Acute neck or back pain * Neck or back pain of unknown etiology * Implants in the neck or back, that are sensitive to magnetic fields

Design outcomes

Primary

MeasureTime frame
Change of tinnitus severity as measured by the tinnitus questionnaireweek 12

Secondary

MeasureTime frame
Change of tinnitus severity as measured by the tinnitus questionnaireweek 2, week 4, week 12
Change of tinnitus severity as measured by numeric rating scalesweek 2, week 4, week 12
Change of depressive symptoms as measured by the major depression inventoryweek 2, week 4, week 12
Change in quality of life as measured by the WHOQoL-Brefweek 2, week 4, week 12
Change in neck pain by the neck pain and disability scaleweek 2, week 4, week 12

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026