Effcet of Temporomandibular Joint Disorder Relaxation and Myofacial Relaxation Techniques on Tension Headache
Effect of Temporomandibular Joint Disorder Relaxation and Myofacial Relaxation Techniques on Quality of Life, Depression and Headache in Individuals With Tension Headache
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Tipo de estudio
Inscripción (Anticipado)
Inscripción
Fase
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Alanya
-
Antalya, Alanya, Pavo
- Alanyaaku
-
-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- individuals diagnosed with tension-type headache by a specialist physician
- individuals diagnosed with Temporomandibular joint dysfunction by dentist-maxillofacial surgeon
- To be able to read and understand Turkish
- Have not received any medical treatment in the last 1 year.
Exclusion Criteria:
- who received physical therapy for TMED in the previous 6 months
- who with any neurological problems
- who with any mental prolems
- who with any konjenital disorders
- who have undergone any cervikal or cranial surgery
- who have any facial trauma or facial paralyses
- who have advanced cervikal disc herniation
- who have ankylosing spondlitis, rhematoid arthritis, fibromyalgia
- who have any cominication problems
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Experimental: Myofascial relaxation technique + Temporomandibular joint release techniques group (n=22)
medical treatment + temporomandibular joint relaxation (temporalis, masseter, and suboccipital muscles) + myofasial release/trigger points (trapezius, rhomboideus, and levator scapulae, sternocleidomastoideus muscles),
|
Control group will be received only medical treatment
|
|
Experimental: Temporomandibular joint release techniques group (n=22)
only temporomandibular joint relaxation will be performed in this group (temporalis, masseter, and suboccipital muscles).
|
Control group will be received only medical treatment
|
|
Experimental: Control group (n=22)
only medication treatment will be applied
|
Control group will be received only medical treatment
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Cervikal region range of motion measurement
Periodo de tiempo: "baseline,preintervention " and "immediately after the intervention"
|
Cases will be shown and asked to perform head flexion, extension, lateral flexion and rotation movements.
And active joint range of motion will be evaluated with goniometer.
|
"baseline,preintervention " and "immediately after the intervention"
|
|
Temporomandibular joint range of motion measurement
Periodo de tiempo: "baseline,preintervention " and "immediately after the intervention"
|
In our study, the maximum mouth opening amount of individuals in the group will be measured with a millimeter ruler 'right , left and side movements of the jaw (laterotrusion), forward movement (protrusion) and back movement (retrusion)'.
|
"baseline,preintervention " and "immediately after the intervention"
|
|
Fonseca Questionnare
Periodo de tiempo: "baseline,preintervention " and "immediately after the intervention"
|
In order to classify Temporomandibular joint dysfunction, the Fonseca questionnaire will be applied.
this questionnaire consists of 10 questions.
Participants are asked to answer each question in the form of Yes (10 points), Sometimes (5 points ), No (0 points).
Scores of all questions are collected and the severity of temporomandibular joint dysfunction is determined.
TMED-No (0-15 points), Mild-TMED (20-40 points), Moderate-TMED (45-60 points) and Severe - TMED (70-100 points).
|
"baseline,preintervention " and "immediately after the intervention"
|
|
Headache Impact Test
Periodo de tiempo: "baseline,preintervention " and "immediately after the intervention"
|
This questionnaire describes the frequency of a person's headache, the degree of restriction in daily life activities and social settings due to headaches , their psychological state , changes in their cognitive function.
|
"baseline,preintervention " and "immediately after the intervention"
|
|
Beck depression scale
Periodo de tiempo: "baseline,preintervention " and "immediately after the intervention"
|
In order to evaluate depression level, The beck depression scale will be used.in
the scale consisting of 21 questions, each question consists of 4 styles.
The questions are scored between 0-3 points dec Low scores represent good results.
According to the scores obtained, (0-9) points indicate minimal depression, (10-16) points indicate mild depression, (17-29) points indicate moderate depression, and (30-63) points indicate severe depression
|
"baseline,preintervention " and "immediately after the intervention"
|
|
Beck Anxiety Sacle
Periodo de tiempo: "baseline,preintervention " and "immediately after the intervention"
|
In order to evaluate anxiety level, The beck depression scale will be used.in
this scale consisting of 21 items, a quadruple Likert type measurement is performed.
0 points = none ,1 point = light , 2 points =medium , 3 points = serious.
the december of 8-15 points is expressed as mild anxiety symptoms, moderate anxiety dec 16-25 points, severe anxiety symptoms from 26-63 points.
|
"baseline,preintervention " and "immediately after the intervention"
|
|
General short form quality of life scale
Periodo de tiempo: "baseline,preintervention " and "immediately after the intervention"
|
In order to evaluate the quality of life, the short form quality of life will be used.SF-36 is a test consisting of 36 items used to obtain information about a person's physical, emotional, and general health status.
This test includes 8 subscales ; mental state ,energy, pain, physical function, limitation due to physical problems, restriction due to emotional problems, social function and general health.
it is evaluated with a score of 0-100 points.dec.
High marks indicate a good state of health.
|
"baseline,preintervention " and "immediately after the intervention"
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Silla de estudio: Hanifegül Taşkıran, Prof. Dr, Istanbul Aydın University
- Director de estudio: Mustafa Zafer DEMİRTAŞ, MD, Alanya Alaaddin Keykubat University
- Director de estudio: Ertan KARAÇAY, MD, Alanya Alaaddin Keykubat University
- Director de estudio: Ahmet ÖZŞİMŞEK, PHD MD, Alanya Alaaddin Keykubat University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Actual)
Finalización primaria
Finalización del estudio (Anticipado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades Cerebrales
- Enfermedades del Sistema Nervioso Central
- Enfermedades del Sistema Nervioso
- Dolor
- Manifestaciones neurológicas
- Enfermedades musculoesqueléticas
- Enfermedades Musculares
- Enfermedades Estomatognáticas
- Trastornos de cefalea primaria
- Trastornos de dolor de cabeza
- Enfermedades de la mandíbula
- Trastornos Craneomandibulares
- Enfermedades mandibulares
- Síndromes de dolor miofascial
- Enfermedades Articulares
- Dolor de cabeza
- Trastornos de la articulación temporomandibular
- Síndrome de disfunción de la articulación temporomandibular
- Dolor de cabeza tipo tensión
Otros números de identificación del estudio
Otros números de identificación del estudio
- 10354421-2021/07-08
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .