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Clinical Trials in Spain / NCT05167656
Recruiting Not applicable

Intraoral Versus Extraoral Manual Therapy in Subjects With Temporomandibular Disorders

NCT05167656 · tracked via the Priya Life Science Spain tracker
Sponsor
University of Alcala
Phase
Not applicable
Started
2022-04-12
Last updated
2024-05-14

Condition(s) studied

Temporomandibular Disorder

Investigational drug(s) / intervention(s)

Intraoral manual therapyExtraoral manual therapyExercise and counselling

Intraoral manual therapy: Six intraoral manual therapy sessions based on ischemic compression and pain pressure release of the temporomandibular region muscles, applied bilateral.

Extraoral manual therapy: Six extraoral manual therapy sessions based on ischemic compression, pain pressure release and pressure sliding of the temporomandibular region muscles, applied bilateral.

Exercise and counselling: Information about etiology, contributing and related factors, natural history and prognostic of the pathology of temporomandibular disorders. Counselling based on: diet, habits like tabacism, stress and anxiety control, physical activity and awareness of dental clenching. Exercise daily program based on active and passive mobility of the temporomandibular joint, stretching exercises and self massage.

Study summary

The aim of this randomized controlled trial is to evaluate the effects of intraoral manual therapy versus extraoral manual therapy and compare them with a control group, in the management of patients with temporomandibular disorders regarding pain, strength, quality of life, disability and anxiety.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Unilateral temporomandibular pain for more than one month. * Older than eighteen. * No previous treatment to temporomandibular pain in the last 3 months. * Diagnosed based on the Diagnostic Criteria for Temporomandibular Disorders (DC/TMD). Exclusion Criteria: * Patients with cervical or cranial trauma or whiplash. * Diagnosed with systemic disease, like rheumatoid arthritis or fibromyalgia. * Diagnosed of any vascular or metabolic disease. * Previous cervical or temporomandibular surgery. * Dental, medicine or any physical therapy treatment in the last 3 months before the beginning of the interventions.

Primary outcome measure(s)

  • Change in pain intensity — Baseline, change from baseline at 3-week, change from baseline at 6-week, at 1 month after treatment, after 3 months after treatment, after 6 months after treatment.
    Pain intensity measured with numerical pain rating scale which ranges from 0 points (no pain) to 10 points (worst imaginable pain)

Trial sites (1)

FacilityCityRegionStatus
University of Alcalá Alcalá de Henares Madrid Recruiting

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Other trials for the same condition

Validation and Evaluation of the Mastication Function in Adults: The Functional Six-minute Mastication Test (F-6MMT). Starting soon
An Algorithm for Approaching Temporomandibular Disorders With Osteopathic Manual Therapy in Patients With Fibromyalgia Recruiting
Electrical Stimulation of the Mandibular Nerve for Pain and Function Management in Temporomandibular Disorders Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05167656 on ClinicalTrials.gov ↗ ← All trials in Spain