Stripping Massage After Thoracoscopy (SMAT)
Primary Purpose
Chest Pain
Status
Unknown status
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Stripping massage
Sponsored by
About this trial
This is an interventional treatment trial for Chest Pain focused on measuring Chest pain; Stripping massage; thoracoscopy; trigger points
Eligibility Criteria
Inclusion Criteria:
- Chest pain with visual analogue scale larger than 3 after thoracoscopic surgery
Exclusion Criteria:
- bleeding tendency
Sites / Locations
- National Taiwan University Hospital Research Ethics CommitteeRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
traditional treatment
Stripping massage
Arm Description
received conventional analgesics.
received SM twice daily in the active trigger points of the rhomboid for two weeks.
Outcomes
Primary Outcome Measures
Change From Baseline in Pain Scores on the Visual Analog Scale
differences of visual analogue scale. (score from mild 0 to severe 10)
Secondary Outcome Measures
demand time of analgesics
demand time of analgesics after thoracoscopic surgery
Full Information
NCT ID
NCT04716816
First Posted
January 17, 2021
Last Updated
January 19, 2021
Sponsor
National Taiwan University Hospital
Collaborators
National Taiwan University Hospital, Yun-Lin Branch
1. Study Identification
Unique Protocol Identification Number
NCT04716816
Brief Title
Stripping Massage After Thoracoscopy
Acronym
SMAT
Official Title
Pain Relief Following Stripping Massage for Rhomboid Myofascial Trigger Points After Thoracoscopic Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 17, 2021 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
Collaborators
National Taiwan University Hospital, Yun-Lin Branch
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study investigated the effects of stripping massage (SM) on myofascial trigger points in the rhomboid after thoracoscopic surgery.
Detailed Description
This study investigated the effects of stripping massage (SM) on myofascial trigger points in the rhomboid after thoracoscopic surgery. Sixty patients with chest pain after thoracoscopic surgery were randomized divided into two equal groups (A and B). Group A (n = 100) received conventional analgesics. Group B (n = 100) received SM twice daily in the active trigger points of the rhomboid for two weeks. The visual analogue scale, a pressure algometer, will be used to evaluate patients' pre- and post-treatment statuses.
This study will compare differences between the current traditional method (using analgesics) and the SM for rhomboid myofascial trigger points for post-thoracoscopic chest pain, and analyze the variables generated by the two different methods including demand time of analgesics, acceptance, and differences of visual analogue scale. The results of the study will use scientific data to prove which way is a good way to take into account of the relief of patient's chest pain.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chest Pain
Keywords
Chest pain; Stripping massage; thoracoscopy; trigger points
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
treatment method and treatment group
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
traditional treatment
Arm Type
No Intervention
Arm Description
received conventional analgesics.
Arm Title
Stripping massage
Arm Type
Experimental
Arm Description
received SM twice daily in the active trigger points of the rhomboid for two weeks.
Intervention Type
Procedure
Intervention Name(s)
Stripping massage
Intervention Description
Stripping massage for rhomboid myofascial trigger points
Primary Outcome Measure Information:
Title
Change From Baseline in Pain Scores on the Visual Analog Scale
Description
differences of visual analogue scale. (score from mild 0 to severe 10)
Time Frame
baseline, 3 days, one weeks, two weeks, one month
Secondary Outcome Measure Information:
Title
demand time of analgesics
Description
demand time of analgesics after thoracoscopic surgery
Time Frame
baseline, 3 days, one weeks, two weeks, one month
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Chest pain with visual analogue scale larger than 3 after thoracoscopic surgery
Exclusion Criteria:
bleeding tendency
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pei-Ming Huang, MD, Ph.D
Phone
+886-23123456
Ext
63509
Email
e370089@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pei-Ming Huang, MD, Ph.D
Organizational Affiliation
National Taiwan University Hospital Yunlin Branch
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Taiwan University Hospital Research Ethics Committee
City
Taipei
ZIP/Postal Code
10002
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pei-Ming Huang, MD, Ph.D.
12. IPD Sharing Statement
Plan to Share IPD
No
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Stripping Massage After Thoracoscopy
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