Effectiveness of Cervical Treatment in Wind Musicians With Temporomandibular Dysfunction

Not Applicable

Completed

• Conditions: Temporomandibular Joint Dysfunction Syndrome
• Interventions: Other: Postural exercises; Other: Manual therapy

• Registration Number: NCT05893251
• Lead Sponsor: Universidad de Murcia

Brief Summary

Temporomandibular dysfunction (TMD) consists of a series of multifactorial signs and symptoms that occur in the orofacial region, with pain being the most common symptom. There is a close biomechanical and anatomical relationship between the cervical region and the temporomandibular joint (TMJ) through the trigemino-spinal nucleus.

Objectives: To comparatively assess the improvement in subjects with TMD when adding cervical manual therapy to a postural treatment. Additionally, to determine if both cervical treatments separately produce changes in the TMJ.

Materials and methods: An experimental study of randomized controlled clinical trial type was conducted. The study involved 30 wind instrument players randomly assigned to an experimental group (EG) and a control group (CG). After obtaining consent, measurements were taken for maximum mouth opening (MMO), cervical range of motion, and pain threshold to pressure (PTP) in the masseter and temporalis muscles. Both groups underwent active cervical postural treatment for 4 weeks, and the EG additionally received a cervical manual therapy protocol. An initial assessment was conducted before the intervention, and a final assessment was done one week after the last intervention. The statistical program SPSS was used for data analysis.

Detailed Description

Not available

Study Timeline

• Study Start: 2017-11-01
• Status Verified: 2018-03
• Primary Completion: 2018-04-01
• Study Completion: 2018-06-01
• Study First Submitted: 2023-05-29
• Study First Submitted QC: 2023-05-29
• Study First Posted: 2023-06-07
• Last Update Submitted: 2023-06-08
• Last Update Posted: 2023-06-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Acceptance of written informed consent.
• Playing a wind instrument.
• Age between 18-40 years.
• Pain in the cranio-cervico-mandibular region and/or masticatory muscles.
• Hypertrophy in the masticatory muscles.

Exclusion Criteria

• History of trauma and/or fracture in the cranial and/or facial region.
• Rheumatic injury or degenerative disease.
• Surgical intervention on the temporomandibular joint (TMJ).
• Malformations of the cervical or cranial spine.
• Vestibular, circulatory, or neurological disorders.
• Degenerative or infectious joint diseases.
• Current orthodontic treatment.
• Receiving physiotherapy treatment during the two weeks prior to the study or during the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Protocol group	Postural exercises	The treatment plan includes active postural exercises for the cervical spine.
Manual therapy group	Manual therapy	The treatment plan includes active postural exercises and manual therapy for the cervical spine.

Primary Outcome Measures

Name	Time	Method
Cranio facial pain and disability inventory	a week after treatment	CF-PDI (Craniofacial Pain and Disability Inventory): This questionnaire focuses on pain as a common symptom of TMD (Temporomandibular Disorders). It is self-administered and designed to assess patients' perception of their physical and psychosocial health in relation to craniofacial pain. It consists of 21 questions regarding the impact of pain on activities involving the use of the temporomandibular joint, with a scoring range from 0 to 63 in ascending order, where 0 indicates no impact and 63 indicates maximum impact. This questionnaire demonstrates good structure, internal consistency, reproducibility, and validity, making it an objective tool that can be used in research and clinical practice for evaluating patients with craniofacial pain and disability. It is easy to administer and requires a short amount of time. The CF-PDI was created and developed in Spain, based on a biopsychosocial approach.

Secondary Outcome Measures

Name	Time	Method
Maximum mouth opening.	a week after treatment	The measurement of maximum mouth opening (MMO) is the distance in centimeters between the upper and lower incisor teeth when the subject actively opens their mouth.

Trial Locations

Locations (1)

University Of Murcia; 🇪🇸 Murcia, Spain