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Traditional Thai Massage and Scapulocostal Syndrome

Efficacy of Traditional Thai Massage on Patients With Scapulocostal Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01168180
Enrollment
60
Registered
2010-07-23
Start date
2010-07-31
Completion date
2011-12-31
Last updated
2012-08-14

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

Conditions

Scapulocostal Syndrome

Keywords

Traditional Thai Massage, Scapulocostal Syndrome

Brief summary

The purpose of this study is to evaluate the efficacy of traditional Thai massage on pain intensity, pressure pain threshold, muscle tension, anxiety, cervical range of motion, patient satisfaction and side effects in the treatment of scapulocostal syndrome.

Interventions

The participants will receive thirty minutes session of traditional Thai massage onto the scapular region for 9 sessions over a period of 3 weeks

Sponsors

Khon Kaen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

1. Male or female 2. Age between 18 - 50 years old 3. The participants have experienced spontaneous scapular pain (VAS ≥ 3) for longer than 12 weeks (chronic) and that at least one trigger point will be present in the scapular region (serratus posterior superior, rhomboid groups, levator scapulae and trapezius muscles). Trigger points will be diagnosed as the presence of focal tenderness in a taut band and with pain recognition. 4. The participants will be able to follow instructions. 5. Good communication and cooperation.

Exclusion criteria

1. A history of the following diseases or disorders: * Rotator cuff disease * Cervical radiculopathy * Degenerative shoulder joint disease * Shoulder stiffness 2. Contraindications of traditional Thai massage * Contagious skin disease * Injury or inflammation of muscle * Bone fracture and/or joint dislocation * Open wound * Uncontrolled hypertension * Drug and/or alcohol intoxication

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity (Visual analog scale)4 monthsThe intensity of pain will be reported by the participant on a numerical analog scale ranging from 0 to 10. Zero indicates no pain anywhere and 10 indicates the most pain ever experienced.

Secondary

MeasureTime frame
Pressure Pain Threshold4 months
Muscle tension (Visual analog scale)4 months
State Anxiety Inventory4 months
patient satisfaction3 weeks
Side effects3 weeks

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026