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Development and Effectiveness of ELMT in Comparison with MCT in Patients with Primary MTD

Development and Effectiveness of Elective Laryngeal Manual Therapy in Comparison with Manual Circumlaryngeal Therapy in Patients with Primary Muscle Tension Dysphonia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211110053027N1
Enrollment
30
Registered
2021-12-18
Start date
2022-04-04
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Muscle Tension Dysphonia (MTD). Voice and resonance disorders

Interventions

Intervention 1: Intervention group: According to the ELMT protocol by the first researcher, this study will be performed twice a week with 30-minute treatment sessions in the speech therapy ward of Am

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: In the present study, those MTD patients will enter the study who have the following criteria: After being informed of the conditions and manner of conducting the study, express their informed consent to participate in the study; 2. Be in the age range of 20 to 55 years and all be women; 3. More than three months have passed since the voice or voice-related complaints; 4. Receive a primary MTD diagnosis based on the consensus of the laryngologist and speech and language pathologist and the results of voice history, consensus auditory-perceptual evaluation of voice, palpation, and video laryngoscopy; Receive voice therapy or other voice-related therapies while performing the study.

Exclusion criteria

Exclusion criteria: Received voice therapy or other voice-related therapies for 90 days prior to the start of the study; Have had an upper respiratory tract infection or a cold during the study and up to three weeks before; Mass, wound or scar, presence of high fat tissue, history of surgery and radiotherapy in the neck area; Be during breastfeeding and pregnancy; Have an addiction to tobacco, drugs and alcohol; There are neurological disorders involving the larynx, hearing disorders, head and neck surgeries, and behavioral and psychological disorders.

Design outcomes

Primary

MeasureTime frame
Voice self-assessment. Timepoint: In the initial assessments, the first and second intermediate assessments and the final assessment. Method of measurement: Each patient's perceptual judgment about their own voice quality is made using a Visual Comparative Scale (VAS) through interviews. In other words, in the present study, a 100 mm line is used to measure sound self-assessment, in which a score of 0 means natural sound quality and a score of 100 means the worst sound quality.;Frequency and severity of vocal tract discomfort. Timepoint: In the initial assessments, the first and second intermediate assessments and the final assessment. Method of measurement: To evaluate the frequency and severity of the discomfort experienced in the vocal tract from the participants' point of view, the Persian version of the VTD scale called VTDp will be used. This scale is a self-perceptual questionnaire that will be provided to patients to comment on the frequency and severity of symptoms in the auditory canal.;Pain, tightness, tenderness, hypertrophy, a trigger point in each of the target muscles, the height of the larynx in the neck, limitation in lateral movement of the larynx, and the size of the thyrohyoid and cricothyroid space. Timepoint: In the initial assessments, the first and second intermediate assessments and the final assessment. Method of measurement: In this study, palpation included examination of pain in the target muscles, tightness in each of the target muscles, sensitivity to palpation in each of the target muscles, hypertrophy in each of the target muscles, trigger points in each of the target muscles, laryngeal height, lateral movement limitation of the larynx is the size of the thyroid space and the size of the cricothyroid space. The evaluation method for each of the above is as follows: palpation is done using the index or middle fingers and the thumbs of both left and right hands while the patient is sitting on a chair and the evaluator is standing behi

Secondary

MeasureTime frame
Overall severity of dysphonia and Strain. Timepoint: Once in the initial assessments and the second time in the final assessments. Method of measurement: To assess the Auditory-perceptual voice assessment, two evaluators will listen to the recorded voice samples. Then, for the index of Overall severity of dysphonia and Strain from the Persian version of Consensus Auditory-perceptual assessment -voice profile (ATSHA), they will record a number between 0 and 100. According to, the (ATSHA) instructions, examples of recorded voice include /a/ and /i/ vowel prolong tasks, sentence reading, and continuous speech.;Voice acoustic features involves the extraction of numerical value Jitter, Shimmer, Harmony to noise ratio, and First, second and third formants. Timepoint: Initial and final evaluations. Method of measurement: Acoustic measurement and analysis of patient voice characteristics is performed using praat software. For this purpose, the person's voice when saying vowels and continuous speech is recorded and analyzed using the mentioned software.;Anteroposterior supraglottic constriction, mediolateral supraglottic constriction, and glottal closure. Timepoint: Initial and final evaluations. Method of measurement: The laryngeal examination is performed by observation and using video laryngoscopy technique by an Ear, Nose, and Throat specialist and Speech and Language Pathologist. After examination and review of video laryngoscopic films, the results related to the supraglottic anterior-posterior compression, supraglottic medial-lateral compression, and the model of the glottal closure were extracted and recorded in the relevant form.;Voice acoustic features involves the extraction of numerical value Jitter, Shimmer, Harmony to noise ratio, and First, second and third formants. Timepoint: Initial and final evaluations. Method of measurement: Acoustic measurement and analysis of patient voice characteristics is performed using praat software. For this purpose, the person'

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmin Rezaee rad

Tehran University of Medical Sciences

aminrezaeerad@gmail.com+98 21 7762 8205

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026