The Association Between Temporomandibular Disorders and Sacroiliac Joint Dysfunction
- Conditions
- Temporomandibular Joint DisordersTemporomandibular Disorder
- Interventions
- Other: Orofacial Manual Therapy
- Registration Number
- NCT06035341
- Lead Sponsor
- Marmara University
- Brief Summary
The aim of this study is to evaluate the relationship between Temporomandibular Disorders (TMD) and Sacroiliac Joint Disfunction (SIJD) and to determine the immediate effect of single-session orofacial manual therapy on SIJD. Patients will be treated for 1 session. The evaluation was planned to be done twice, at the beginning and end of the session.
- Detailed Description
The aim of this study is to evaluate the relationship between TMD and SIJD and to determine the immediate effect of single-session orofacial manual therapy on SIJD. Patients diagnosed with both TMD and SIJD will be participants of the study. Patients will be treated for 1 session. Immediately after the treatment, participants will be asked to walk for 5 minutes, after which a second assessment will be done. The evaluation was planned to be done twice, at the beginning and end of the session. Pressure pain threshold, joint range of motion, functionality, and sacroiliac joint disfunction will be evaluated by using digital algometer, ruler, "Oswestry Disability Index (ODI)" and specific tests respectively.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 23
- Volunteered to participate,
- Aged between 18-60 years old,
- Having the diagnosis of Temporomandibular Disorders (TMB) and sacroiliac joint disfunction (SIJD),
- Having a malignant condition, trauma and surgery of the cranial and cervical region,
- Not being cooperative,
- Regular use of analgesic and anti-inflammatory drugs,
- Having dentofacial anomalies,
- Having active inflammatory arthritis,
- Having metabolic diseases (Gout, osteoporosis, Cushing's disease and hyper/hypo-parathyroidism),
- Having connective tissue, rheumatological (Systemic lupus erythematosus and scleroderma) and hematological disorders (Anemia and leukemia),
- Having a diagnosed psychiatric illness,
- Receiving TMD-related physical therapy less than 6 months ago
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Treatment Group Orofacial Manual Therapy Participants in this group will be received orofacial manual therapy as treatment. The number of participants is planned to be 23.
- Primary Outcome Measures
Name Time Method Fifth Test for Sacroiliac Joint Disfunction: Sacral Thrust Test Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. The patient lies in a prone position. The practitioner places one hand on the apex of the sacrum while applying direct pressure with the other hand. Pathology in the SI joint is considered if pain occurs in the hip.
Pain Threshold: Digital algometer Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. The algometer is a reliable instrument for measuring the sensitivity of the masticatory muscles and 1 cm below the Posterior Superior Iliac Spine (PSIS). The measurement will be made at 10 points. A force (Newton in force) of 1 kg (weight in kilogram) per square centimeter (surface area in centimeter square) is applied to the patient for 3 seconds, and this is continued until the patient feels pain (weight and surface area will be combined to report Newton in kg/ cm2). This process will be repeated three times and the average value will be calculated.
Range of Motion Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. Mouth opening, protrusion and right and left lateral deviation will be measured starting from 0 using a 15 cm ruler. Repeated measuring reduces the standard error of measurement, hence repeated measurements will be also included in our study (three times) with the largest recorded range taken.
First Test for Sacroiliac Joint Disfunction: Distraction Test Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. The patient lies in a supine position. Direct posterolateral pressure is applied to the bilateral anterior superior iliac spines, thus stressing the anterior sacroiliac ligament. Pathology in the Sacroiliac (SI) joint is considered if pain occurs in the hip.
Fourth Test for Sacroiliac Joint Disfunction: Gaenslen Test Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. The patient lies in a supine position close to the edge of the bed. The patient draws his leg toward the abdomen so as to place the knee and hip in flexion. The outside leg (closest to the practitioner) is allowed to hang down from the examination table, while the SI joint is contracted by placing pressure on the inside (furthest from the practitioner) iliac crest and outside leg. Pain indicates pathology of the SI joint on the tested side.
Sixth Test for Sacroiliac Joint Disfunction: Faber (Patrick) Test Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. The patient lies in a supine position, while the practitioner stands beside the patient and bends the patient's knee, bringing the heel to the opposite knee. With the other hand, the practitioner ensures that the contralateral anterior superior iliac spine remains in a neutral position. The physician applies mild pressure to the bent knee. Pressure is assumed to be applied to the bilateral SI ligaments and hip joints. Pathology in the SI joint is considered if pain occurs in the hip. Pain provocation occurs with flexion, adduction and external rotation of the hip.
Second Test for Sacroiliac Joint Disfunction: Compression Test Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. The patient lies on his side with the affected side on top, with the hip at 45° flexion and the knees at 90° flexion. The physician stands behind the patient and applies pressure to the pelvis over the iliac crest directly toward the contralateral iliac crest. This test can be applied in a supine or prone position. Pathology in the SI joint is considered if pain occurs in the hip.
Third Test for Sacroiliac Joint Disfunction: Thigh Thrust Test Change between baseline (immediately before intervention) and post intervention (immediately after intervention). The intervention is one hour. The patient lies in a supine position. The hip is brought to 90º flexion. Pressure is applied directly toward the examination table. Pathology in the SI joint is considered if pain occurs in the hip. Pain provocation is established with hip flexion and adduction.
- Secondary Outcome Measures
Name Time Method Oswestry Disability Index (ODI) for Functional Low Back Pain Change between baseline (immediately before intervention) and 1 week post intervention. The intervention is one hour. Oswestry Disability Index (ODI) will be used to evaluate low back pain. ODI consists of 10 items on the degree of severity to which low back trouble has affected the ability to manage in everyday life. The 10 sections cover the pain and the daily function (including pain intensity, personal hygiene, lifting, walking, sitting, standing, sleeping, sexual activity, social activity, and traveling). Each item is rated on a 6-point scale (0-5); the higher score means the higher level of disability related to low back pain.
Trial Locations
- Locations (1)
Sultan İğrek
🇹🇷Istanbul, Turkey