Effect of Ischemic Compression With Stretching on Patients With Upper Back Pain
Primary Purpose
Myofascial Pain Syndrome
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Ischemic compression with stretching
Sponsored by
About this trial
This is an interventional treatment trial for Myofascial Pain Syndrome
Eligibility Criteria
Inclusion Criteria:
- The participants have experienced spontaneous upper back pain for longer than 12 weeks (chronic) and that at least one trigger point will be present in the s trapezius muscles. 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:
- Fibromyalgia syndrome
- Cervical radiculopathy or myelopathy)
- Cervical spine surgery
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Ischemic compression with stretching
Control
Arm Description
The participants will receive the ischemic compression with stretching onto the trapezius muscle
Rest on the bed
Outcomes
Primary Outcome Measures
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
Secondary Outcome Measures
Pressure Pain Threshold as a measure by pressure algometry
Anxiety on State Anxiety Inventory
Cervical range of motion
Patient satisfaction level
Full Information
NCT ID
NCT02437292
First Posted
May 5, 2015
Last Updated
May 6, 2015
Sponsor
Mae Fah Luang University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02437292
Brief Title
Effect of Ischemic Compression With Stretching on Patients With Upper Back Pain
Official Title
Effect of Ischemic Compression With Stretching on Pain Related Parameters in Patients With Upper Back Pain Associated With Myofascial Trigger Point
Study Type
Interventional
2. Study Status
Record Verification Date
May 2015
Overall Recruitment Status
Unknown status
Study Start Date
May 2015 (undefined)
Primary Completion Date
August 2015 (Anticipated)
Study Completion Date
August 2015 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mae Fah Luang University Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine the effect of ischemic compression with stretching on pain related parameters including pain intensity, pressure pain threshold, anxiety, cervical range of motion and patient satisfaction in patients with scapular pain associated with myofascial trigger point.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myofascial Pain Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Ischemic compression with stretching
Arm Type
Experimental
Arm Description
The participants will receive the ischemic compression with stretching onto the trapezius muscle
Arm Title
Control
Arm Type
No Intervention
Arm Description
Rest on the bed
Intervention Type
Other
Intervention Name(s)
Ischemic compression with stretching
Primary Outcome Measure Information:
Title
Pain score on Visual analog scale
Description
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
Time Frame
5 weeks
Secondary Outcome Measure Information:
Title
Pressure Pain Threshold as a measure by pressure algometry
Time Frame
5 weeks
Title
Anxiety on State Anxiety Inventory
Time Frame
5 weeks
Title
Cervical range of motion
Time Frame
5 weeks
Title
Patient satisfaction level
Time Frame
5 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The participants have experienced spontaneous upper back pain for longer than 12 weeks (chronic) and that at least one trigger point will be present in the s trapezius muscles. 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:
Fibromyalgia syndrome
Cervical radiculopathy or myelopathy)
Cervical spine surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
VITSARUT BUTTAGAT, Ph.D.
Phone
66882674423
Email
vitsarutbut@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
VITSARUT BUTTAGAT, Ph.D.
Organizational Affiliation
Mae Fah Luang University
Official's Role
Principal Investigator
12. IPD Sharing Statement
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Effect of Ischemic Compression With Stretching on Patients With Upper Back Pain
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