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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02437266
Other study ID # 55218152-5
Secondary ID
Status Not yet recruiting
Phase N/A
First received May 5, 2015
Last updated May 6, 2015
Start date May 2015
Est. completion date August 2015

Study information

Verified date May 2015
Source Mae Fah Luang University Hospital
Contact VITSARUT BUTTAGAT, Ph.D.
Phone 66882674423
Email vitsarutbut@hotmail.com
Is FDA regulated No
Health authority Thailand: School of Health Science, Mae Fah Luang University Ethics Committee for Human Research
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effect of scapular mobilization on pain related parameters including pain intensity, pressure pain threshold, muscle tension, anxiety, Scapular range of motion, patient satisfaction in patients with scapular pain associated with myofascial trigger point:


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 38
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- The participants have experienced spontaneous scapular pain for longer than 12 weeks (chronic) and that at least one trigger point will be present in the muscles surrounding the scapula. Trigger points will be diagnosed as the presence of focal tenderness in a taut band and with pain recognition.

- The participants will be able to follow instructions.

- Good communication and cooperation.

Exclusion Criteria:

- Shoulder impingement syndrome

- Adhesive capsulitis

- Shoulder instability

- Shoulder arthritides

- Shoulder dislocation and/or bone fracture

- Hypermobility of shoulder joint

- Open wound

- Drug and/or alcohol intoxication

- Contraindications of mobilization

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Other:
Scapular mobilization


Locations

Country Name City State
Thailand School of Health Science, Mae Fah Luang University Mueang Chiang Rai

Sponsors (1)

Lead Sponsor Collaborator
Mae Fah Luang University Hospital

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain score on Visual analog scale The intensity of pain will be reported by the participant on a visual analog scale ranging from 0 to 10. Zero indicates no pain anywhere and 10 indicates the most pain ever experienced. 5 weeks Yes
Secondary Pressure Pain Threshold as a measure by pressure algometry 5 weeks Yes
Secondary Anxiety on State Anxiety Inventory 5 weeks Yes
Secondary Scapular range of motion 5 weeks Yes
Secondary Patient satisfaction level 5 weeks Yes
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