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Movement therapy in patients with scapulocostal syndrome and masticatory myofascial pain

Movement therapy in patients with scapulocostal syndrome and masticatory myofascial pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190512001
Enrollment
Unknown
Registered
2019-05-12
Start date
2019-05-10
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

The patients with scapulocostal syndrome and masticatory myofascial pain&#44

Interventions

Participants in the control group will be received the usual care and education with home physical therapy for 30 minutes in total. The programs will be conducted 3 times a week for 4 weeks. For the r
etc.,The participants in this group will be received the usual care and education with home physical therapy for 30 minutes. After that&#44
they will be received the movement therapy technique for 30 minutes. The total time will be approximated 60 minutes and will be performed 3 times a week for 4 weeks.
Active Comparator Other,Experimental Other

Sponsors

Human High Performance and Health Promotion Research Institute, Khon Kaen University
Lead Sponsor
Human High Performance and Health Promotion Research Institute&#44
Collaborator
Khon Kaen University
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Female and male age between 18 to 50 years 2. Present pain at medial scapular region at least 3 points and the most painful area will be recorded for each participant 3. Present pain at the masticatory muscles at least one point, and the most painful area will be recorded for each participant. 4. Present pain longer than 3 months 5. Present with moderate pain (VAS score more than 3) 6. Presence of both clicking and not clicking joint sound without joint pain. 7. Presence of a maximum range of motion of mouth opening less than 40 mm or presence of pain with a full range of motion. 8. Able to follow the instructions 9. Good consciousness and co-operation

Exclusion criteria

Exclusion criteria: 1. TMD with disc displacement and osteoarthritis (Axis I, group II, and group III) 2. A history of the following diseases or disorders - Systemic disease including cardiovascular, pulmonary, gastrointestinal, urogenital, endocrine, nervous system, and integumentary disease. - Serious condition including accident, spinal fractures, spinal or central cord compression, neoplastic, vascular compromise, system or inflammatory diseases, and upper cervical spine ligamentous instability - Another type of headache including migraine with aura, tension-type headache with central sensitization, and cervicogenic headache. - Unable to follow the instructions

Design outcomes

Primary

MeasureTime frame
Pain intensity Baseline, immediate, after the last treatment, and at 1 month follow up Visual analog scale (VAS)

Secondary

MeasureTime frame
Pressure pain threshold Baseline, immediate, after the last treatment, and at 1 month follow up Pressure algometer,Maximum mouth opening Baseline, immediate, after the last treatment, and at 1 month follow up Therabite range of motion scale,Craniovertebral angle Baseline, immediate, after the last treatment, and at 1 month follow up Three-point Marker detection software method ,Pain diary During the follow up period Paper of pain diary,Mouth opening Baseline, immediate, after the last treatment, and at 1 month follow up Therabite range of motion scale,Cortisol level Baseline and after the first treatment ELISA kit (salivary test)

Countries

Thailand

Contacts

Public ContactWilawan Kanhachon

School of Physical Therapy, Faculty of Associated Medical Science, Khon Kaen University, Khon Kaen P

oam_konkai_tt@hotmail.com0951695055

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026