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A pilot study on the development of a massage formula for Lam Plai Patakat (Saiyan 4) Syndrome and the evaluation of its effectiveness in affected patients.

A pilot study on the development of a massage formula for Lam Plai Patakat (Saiyan 4) Syndrome and the evaluation of its effectiveness in affected patients.

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260706004
Enrollment
16
Registered
2026-07-06
Start date
2026-07-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Upper back pain syndrome Upper back pain syndrome Lam Plai Patakat (Saiyan 4) massage Thai massage

Interventions

Conventional Thai traditional massage Massage at four shoulder points on each side for 15 seconds per point Massage of the cervical and cervicothoracic regions for 45 seconds per point Massage of the
Active Comparator Other,Experimental Other
Conventional Thai traditional massage ,Modified Thai Traditional Massage

Sponsors

Faculty of Medicine, Thammasat University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosed with Lom Plai Patkhat Signal 4 (Posterior Type), characterized by pain in the neck, shoulder, and scapular regions, radiating numbness along the lateral aspect of both arms, and tenderness at the shoulder and scapular regions (Foundation for the Rehabilitation and Promotion of Thai Traditional Medicine, Ayurveda School, 2005). 2.Regularly engaged in computer work or smartphone use for at least 2 hours per day. Duration of symptoms of at least 2 weeks. 3.Pain intensity score between 3 and 7 on the Visual Analog Scale (VAS) for neck, shoulder, and scapular pain. 4.Willing and able to provide written informed consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. History of cervical radiculopathy, suspected cervical nerve compression, cervical spondylosis, bleeding disorders, or osteoporosis. 2. Any contraindication to massage therapy. 3. Pregnancy, confirmed by medical history or a pregnancy test. 4. Hemiplegia or paresis. 5. Thrombophlebitis. 6. History of diabetes mellitus, hypertension, or cardiovascular disease. Current use of anticoagulant or antiplatelet medications, such as aspirin, clopidogrel, prasugrel, or ticlopidine. 7. Use of analgesics, anti-inflammatory drugs (e.g., NSAIDs or acetaminophen), massage therapy, physical therapy, or other treatments for musculoskeletal pain within 24 hours prior to enrollment. Withdrawal/Discontinuation Criteria 1. Use of analgesics, anti-inflammatory drugs, anticoagulants, or any treatment for muscle pain during the 1-week follow-up period. 2. Failure to attend the 1-week follow-up assessment. 3.Dizziness or a sensation of impending fainting during massage treatment. Worsening of symptoms, including increased pain intensity, swelling, bruising, and tenderness upon palpation.

Design outcomes

Primary

MeasureTime frame
Visual analog scale Baseline, immediately after treatment, and 1 week after treatment Pain intensity measured using a 10-cm Visual Analog Scale (VAS), score ranging from 0 (no pain) to 10 (worst imaginable pain)

Secondary

MeasureTime frame
Neck Disability Index Baseline, immediately after treatment, and 1 week after treatment Neck disability measured using the Neck Disability Index (NDI), total score ranging from 0 to 50,Algometer Baseline, immediately after treatment, and 1 week after treatment Pressure pain threshold measured using a pressure algometer and expressed in kg/cm2 or newtons,Cervical Range of Motion Baseline, immediately after treatment, and 1 week after treatment Cervical range of motion measured in degrees

Countries

Thailand

Contacts

Public ContactNichamon Mukkasombut

Thammasat University

nschamon@tu.ac.th029269749

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026