Instrument Assisted Soft Tissue Mobilization Versus Trigger Points Release on Upper Trapezius Trigger Points

Not Applicable

Completed

• Conditions: Trigger Points

• Registration Number: NCT05249660
• Lead Sponsor: Riphah International University

Brief Summary

Study will be randomized clinical trial. Data will be collected from non probability consecutive sampling technique. Total 30 participants from Ganga Ram Hospital and Care medical centre will be selected and randomly allocated to two different groups i.e Group A and Group B. . Group A will be treated by trigger point release. Group B will be treated by Instrument assisted soft tissue release. NPRS, GONIOMETRY, NDI will be used as outcome measuring tool before and after treatment. Data will be analyzed by using Statistical package for social sciences 25.

Detailed Description

Trigger point is defined as a hyperirritable palpable nodule contained in the skeletal muscle fibers. The palpable nodule, also named taut band, is described as a limited number of fibers with an increased stiffness. Trp causes the muscles to week and stiff, leading to reduction in range of movement. MTrP can produce local and referred pain, either on manual compression or spontaneously.

Instrument-assisted soft tissue mobilization (IASTM) is the use of hard tools to manipulate soft tissue and was derived from the Cyriax1 cross-friction massage. It has recently emerged as a popular alternative to traditional manual therapy techniques. Modern-day IASTM instruments vary in material (e.g. stainless steel, plastic) and design and are used to improve a variety of musculoskeletal conditions and associated outcomes.

Manual technique that uses direct vertical pressure to the TP, is a well-established treatment method used to resolve the TP-related pain syndrome. This directed pressure is managed according to the therapist's perception of the tissue resistance of the treated soft tissue or according to the pain perceived by the patient based on a pain scale. Manual therapy is a commonly used treatment for MPS as it has been considered one of the most effective techniques for the inactivation of MTrPs.

Study Timeline

• Study Start: 2022-01-25
• Study First Submitted: 2022-02-04
• Study First Submitted QC: 2022-02-20
• Study First Posted: 2022-02-22
• Primary Completion: 2022-07-13
• Study Completion: 2022-07-13
• Status Verified: 2022-11
• Last Update Submitted: 2022-11-24
• Last Update Posted: 2022-11-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• Patients with neck pain in the upper trapezius muscle
• Tender nodule, constant pain, a jump sign during palpation will be included in this study

Exclusion Criteria

• Patients with Whiplash injury
• History of neck/shoulder surgery
• Cervical Radiculopathy
• History of malignancy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Numeric pain rating scale	6 weeks	Scale consists of 4 questions regarding actual pain level, zero indicates no pain and 10 indicates worst pain imaginable
Neck disability index	6 weks	Scale consists of 10 sections,each section contains questions regarding head/ neck pain and some questions regarding the daily activities that we perform
Goniometry	6 weeks	Goniometer is used to measure the ranges of body joints.

Trial Locations

Locations (1)

Ganga Ram Hospital and Care medical centre; 🇵🇰 Lahore, Punjab, Pakistan