Effectiveness of Manual Therapy in Patients With Tinnitus and Temporomandibular Joint Disorder.
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ClinicalTrials.gov Identifier: NCT02850055 |
Recruitment Status :
Completed
First Posted : July 29, 2016
Last Update Posted : November 28, 2018
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Tinnitus | Other: Conventional Physiotherapy Other: Specific Manual Therapy | Not Applicable |

Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 64 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Participant, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Effectiveness Specific Manual Therapy in a Multimodal Physical Therapy Treatment in Patients With Tinnitus and Temporomandibular Joint Disorder. |
Actual Study Start Date : | January 2017 |
Actual Primary Completion Date : | May 2018 |
Actual Study Completion Date : | June 15, 2018 |

Arm | Intervention/treatment |
---|---|
Experimental: Specific Manual Therapy Group
Conventional Physiotherapy and Specific manual therapy, six one hour treatment sessions. An hour for week.
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Other: Specific Manual Therapy
Other Name: Manual Therapy |
Active Comparator: Multimodal Group
Conventional Physiotherapy, six one hour treatment sessions. An hour for week.
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Other: Conventional Physiotherapy
Other Name: Multimodal Group |
- Change from baseline Intensity of Temporomandibular Joint pain. [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Intensity of TMJ pain (measured by NPRS) at rest.
- Change from baseline of tinnitus severity. [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Intensity of tinnitus (measured by VAS) at rest. It will be determined by assessing tinnitus annoyance and tinnitus loudness and the average will be recorded.
- Change from baseline degree of tinnitus-related handicap [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Degree of disability caused by tinnitus (measured with the Tinnitus Handicap Inventory (THI).
- Change from baseline degree of disability caused by temporomandibular disorder [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Degree of disability caused by temporomandibular disorder (measured by Craniofacial Pain and Disability Inventory (CF-PDI)).
- Change from baseline quality of life. [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Quality of life, measured with a previously validated Spanish version of the SF-12 (Short Form Health Survey).
- Change from baseline emotional state (depressive symptoms) [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Emotional state of the patient (measured with Beck questionnaire).
- Change from baseline pressure pain sensibility [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Pain sensibility to pressure (measured with an algometer) in the masseter, temporal and lateral pterygoid muscles (over the TMJ).
- Change from baseline range of motion [ Time Frame: At baseline, 1 week post-treatment, and 3 and 6 months post-treatment ]Range of motion of the temporomandibular joint in the mouth opening and bilateral excursion movements (measured in millimetres)

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Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- ≥ 18 and ≤ 65 years old.
- Suffering from tinnitus and temporomandibular dysfunction with a myofascial or joint dysfunction origin: diagnosis of tinnitus attributed to TMD
- In a subacute and chronic phase.
Exclusion Criteria:
- Non signature of the informed consent.
- Patients with a diagnosis of ENT and / or neurological problems from which could arise tinnitus and / or the temporomandibular pain.
- Inability to read, understand and complete questionnaires, read and understand a brochure, or understand and follow verbal commands (e.g. Illiteracy, dementia or blindness).
- Having received physiotherapy in the last 12 months.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02850055
Spain | |
María José Díaz Arribas | |
Madrid, Spain, 28040 |
Study Director: | María J Díaz, Professor | Physiotherapy Professor |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | MARIA JOSE DIAZ ARRIBAS, Tenured University Professor, Universidad Complutense de Madrid |
ClinicalTrials.gov Identifier: | NCT02850055 |
Other Study ID Numbers: |
MJD_2016 |
First Posted: | July 29, 2016 Key Record Dates |
Last Update Posted: | November 28, 2018 |
Last Verified: | November 2018 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
physiotherapy, Temporomandibular Joint Disorder, tinnitus. |
Temporomandibular Joint Disorders Temporomandibular Joint Dysfunction Syndrome Tinnitus Joint Diseases Hearing Disorders Ear Diseases Otorhinolaryngologic Diseases Sensation Disorders Neurologic Manifestations |
Nervous System Diseases Musculoskeletal Diseases Craniomandibular Disorders Mandibular Diseases Jaw Diseases Muscular Diseases Stomatognathic Diseases Myofascial Pain Syndromes |