- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06556758
Stripping Massage on Rhomboid Major and Minor Active Trigger Points in Upper Thoracic Pain
Effects of Stripping Massage on Rhomboid Major and Minor Active Trigger Points in Patients With Upper Thoracic Pain.
Study Overview
Status
Intervention / Treatment
Detailed Description
Spine pain is a common condition that results in considerable levels of disability and lost work time and has a major impact on society, a lifetime prevalence ranging from 15.6% to 19.5% for thoracic pain. Thoracic pain is more prevalent in women than in men (2:1). The origin of spine pain is clearly multifactorial and often includes number of anatomical structures. One plausible etiology of symptoms associated with thoracic pain may be the presence of myofascial pain. Myofascial pain is generally associated with the presence of trigger points. Trigger points are hypersensitive spots within taut bands of skeletal musculature whose stimulation can be associated with referred pain and autonomic phenomena. Trigger points can be either active or latent depending on the association with symptoms. For instance, active trigger points (MTrPs) are associated with spontaneous pain, and the local and referred pain reproduces the symptoms of the patient, totally or partially.
Stripping massage (SM) is a gliding tissue massage technique that focuses on the deeper layers of the fascia and skeletal muscle.This technique involves gliding pressure along a muscle, usually from one attachment to the other in the direction of the muscle fibers. Applying SM to tender spots in muscles can cause ischaemia followed by reflexive hyperaemia. This increases the local blood flow, which improves pliability of the muscles and fascia and helps break down adhesions and decrease pain sensations. SM acts as a mechanical stress that stimulates parasympathetic activity which leads to the release of substances such as endorphins. These chemicals remove the noxious stimulus and decrease the pressure on nociceptors, reducing pain The rationale for the use of this technique is to identify the effects of stripping massage on rhomboids active trigger points in upper thoracic pain patients. This study will see the effects of stripping massage on rhomboids trigger points on pain, thoracic mobility, and functional performance. Aim of this study is to see the effects of stripping massage to figure out whether this technique would be more effective and should be incorporated into clinical settings in relation to conventional treatment.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Madiha Ali, MS-OMPT
- Phone Number: 0331-3360064
- Email: madiha.ali@riphah.edu.pk
Study Locations
-
-
Punjab
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Rawalpindi, Punjab, Pakistan, 44000
- Recruiting
- Railway General Hospital
-
Principal Investigator:
- Aqsa Mustafa, MS-OMPT
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Participants falling in this category would be recruited into the study.
- females
- Age: 18-40
- Active TrPs in the rhomboid major and minor muscles.
- Presence of atleast one trigger point in rhomboids (diagnosed by the characteristics like hyperirritable spot in a taut band, twitch response and referral pain)
- Presence of Jump sign
- Segmental hypomobility in upper thoracic region identified with positive springing test
- upper thoracic pain, defined as pain in the body region encompassing from T1 to T4) pain intensity score of ≥ 3 on the numeric pain rating scale (0-10)
- symptoms provoked by thoracic movement,or palpation of the rhomboid muscles.
Exclusion Criteria:
Participants falling in this category would be excluded from the study.
- a history of neck trauma
- previously had surgery in the neck or shoulder area or suffered from physical injury
- Fractures, Dislocations, Traumatic injuries, Adhesive capsulitis, thoracic outlet syndrome.
- any rheumatic condition, osteoporosis, cancer, spinal infection, radicular pain, or neuropathy.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: stripping massage + conventional Therapy
Stripping Massage Stripping massage on rhomboid major and minor active trigger point in the direction of muscle fiber from origin to insertion of muscle. Frequency: 3 minutes for 3 times/week for 4 consecutive weeks. Conventional therapy including Hot pack for 10 minutes + ischemic compression for 90 secs + CPA glides grade 3 kaltenborn mobilization on thoracic T1 to T4 (5 reps x 1 set) Frequency: 3 times/ week for 4 weeks |
Stripping massage on rhomboid major and minor active trigger point in the direction of muscle fiber from origin to insertion of muscle.
Frequency: 3 minutes for 3 times/week for 4 consecutive weeks.
Conventional PT including Hot pack for 10 minutes + ischemic compression for 90 secs + CPA glides grade 3 kaltenborn mobilization on thoracic T1 to T4 (5 reps x 1 set) Frequency: 3 times/ week for 4 weeks
Other Names:
|
|
Active Comparator: Conventional therapy
Conventional Therapy Conventional PT including Hot pack for 10 minutes + ischemic compression for 90 secs + CPA glides grade 3 kaltenborn mobilization on thoracic T1 to T4(5 reps x 1 set ) Frequency : 3 times/ week for 4 weeks
|
conventional therapy including Hot pack for 10 minutes + ischemic compression for 90 secs + CPA glides grade 3 kaltenborn mobilization on thoracic T1 to T4 (5 reps x 1 set ) Frequency : 3 times/ week for 4 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale NPRS
Time Frame: 4 weeks
|
The NPRS is a segmented numeric version of the visual analog scale which is used to assess pain.
It scores ranges from 0-10, 0 means No pain and 10 means Severe pain.
Patient will be asked to verbally report the pain score.
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Bubble inclinometer
Time Frame: 4 weeks
|
It is an instrument that measures the available range of motion at a joint.
|
4 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional rating index
Time Frame: 4 weeks
|
The Functional Rating Index (FRI) is an instrument specifically designed to quantitatively measure the subjective perception of function and pain of the spinal musculoskeletal system in a clinical environment
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Madiha Ali, MSOMPT, Riphah International University
- Principal Investigator: Aqsa Mustafa, MSompt*, Riphah International University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Aqsa Mustafa
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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