Effectiveness of myofascial trigger point therapy in patients with chronic neck and/or arm pai
Not Applicable
Completed
- Conditions
- Patients with chronic neck and/or arm painMusculoskeletal - Other muscular and skeletal disordersPhysical Medicine / Rehabilitation - Physiotherapy
- Registration Number
- ACTRN12616000901404
- Lead Sponsor
- ational Yang-Ming University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
1.Aged 20-65 patients with chronic neck and/or arm pain
2.Pain intensity (numeric rating scale)>3
3.Presence of active trigger point in at least one of the five following muscles: upper trapezius, levator scapulae, sternocleidomastoid, scalene, splenius cervicis
Exclusion Criteria
1. Neck surgery during the previous 12 months
2. Pregnancy
3. Administration of anti-inflammatory analgesics over the preceding 24 hours
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain intensity assessed by numeric rating scale (NRS).<br><br>[Baseline, immediately after one session intervention, and at 2 days after intervention];Primary Outcome 2: Cervical active/pain-free range of motion assessed by cervical-range-of-motion measurement device<br>[Baseline, immediately after one session intervention, and at 2 days after intervention]
- Secondary Outcome Measures
Name Time Method Pressure pain threshold assessed by digital algometer<br>[Baseline, immediately after one session intervention, and at 2 days after intervention<br>];Tight feeling assessed by 10-point likert scale<br><br>[Baseline, immediately after one session intervention, and at 2 days after intervention];Functional activity assessed by patient specific-functional scale (PSFS)<br>[Baseline, immediately after one session intervention, and at 2 days after intervention];Disability assessed by neck disability index (NDI)<br><br>[Baseline, immediately after one session intervention, and at 2 days after intervention]