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Auriculotherapy in Tension-type Headache Due to Temporomandibular Dysfunction

Not Applicable
Completed
Conditions
Tension-Type Headache
Registration Number
NCT02309775
Lead Sponsor
Federal University of Minas Gerais
Brief Summary

Objectives: Verify the effect of auriculotherapy in patients with tension-type headache resulting from temporomandibular dysfunction.

Design: Randomized clinical study Setting: Randomized Study Participants: The study consist of 38 participants randomized into two groups: an intervention group (n = 18, sample loss = 1) and placebo group (n = 20, sample loss = 6) Interventions: The intervention group will receive treatment with auricular acupuncture in the Shen Men, Kidney, Sympathetic, Subcortex, Adrenal and Cerebral points. The placebo group will receive auriculotherapy in the trachea point.

Main outcome measures: visual analog scale for pain pain (VAS) and surface electromyography (EMG).

Detailed Description

This is an experimental clinical trial in which will be selected at the University, 40 students with tension-type headache due to temporomandibular dysfunction. Among the selected subjects will be randomized by blind draw into two groups: intervention group (IG) and placebo group (GII).

The instruments that will be used for the evaluation are the visual analog pain scale, the Survey questionnaire for Temporomandibular Disorders (RDC) 3, and surface electromyography (EMG System of Brazil).

The EMG signals will be collected in the rest position (3 samples) and maximum voluntary isometric contraction (3 collections). The masseter and temporalis muscles bilaterally will be evaluated according to the protocol of Rodrigues.

For treatment of Ear, initially cleaning the pinna is made to be manipulated with 70% alcohol and later will be inserted mustard seed with a tape in the following points: Shenmen, Sympathetic, Kidney, subcortex, Adrenal and Brain second Souza in GI and GII point of the trachea. Such treatment will last 15 minutes each session, being held 2 times a week, alternating the ear to be manipulated over a period of 5 weeks.

For comparison between groups the Mann-Whitney test statistic with Software BioStat 4.0 software will be used. With a significance level (p \<0.05).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
38
Inclusion Criteria
  • Individuals with tension-type headache due to temporomandibular dysfunction, aged 20 to 30 years, of both sexes
Exclusion Criteria
  • Individuals with migraine type headache, secondary headaches
  • Use of medicines more than 10 days per month and any type of acupuncture treatment in the last 12 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Pattern of muscle contraction (Electromyographic signals of the masseter and temporalis muscles bilaterally.)one day

Electromyographic signals of the masseter and temporalis muscles bilaterally.

Secondary Outcome Measures
NameTimeMethod
Pain at the time (Visual analog pain scale)one week

Pain at the time will using Visual analog pain scale.

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