- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07368426
Immediate Effects of Strain Counterstrain Versus Fascial Distortion Model on Upper Trapezius Latent Trigger Points
Immediate Effects of Strain Counterstrain Versus Fascial Distortion Model on Pain and Function in Individuals With Latent Myofascial Trigger Points of the Upper Trapezius: A Pilot Study
Study Overview
Status
Intervention / Treatment
Detailed Description
Musculoskeletal pain of the cervical region is a prevalent health problem, and the upper trapezius muscle is frequently involved due to postural overload and mechanical stress. These factors are commonly associated with the development of latent myofascial trigger points, which may restrict range of motion and impair neuromuscular function even in the absence of spontaneous pain.
Various manual therapy techniques have been used to manage myofascial trigger points. Strain counterstrain (SCS) is an indirect, low-intensity technique that aims to reduce nociceptive input and muscle spindle activity by positioning the body in a pain-free posture. In contrast, the fascial distortion model (FDM) is a direct manual therapy approach that applies relatively high-intensity pressure to specific fascial distortions identified through patient body language and palpation.
This study was designed as a pilot, parallel-group, pre-post comparative trial to explore the immediate effects of SCS and FDM on pain-related and neuromuscular outcomes in individuals with latent myofascial trigger points of the upper trapezius. Twenty healthy adults were randomly assigned to receive a single session of either SCS or FDM. Cervical range of motion, joint position error, pressure pain threshold, and cervical muscle strength were assessed before and immediately after the intervention. The findings of this study are intended to provide preliminary evidence to inform future large-scale clinical trials comparing manual therapy techniques with differing stimulation characteristics.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Gyeongsangnam-do
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Changwon, Gyeongsangnam-do, South Korea, 51767
- Kyungnam University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Healthy adults aged 18 to 39 years.
- Presence of latent myofascial trigger points in the upper trapezius muscle.
- No history of neurological or orthopedic disorders within the past six months.
- Willingness to participate and provision of written informed consent.
Exclusion Criteria:
- Current or previous complaints of neck or shoulder pain.
- Ongoing treatment for musculoskeletal conditions.
- History of physical therapy or chiropractic treatment within the past six months.
- History of surgery or trauma involving the head or upper trunk.
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 |
|---|---|
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Experimental: Strain Counterstrain Group
Participants received a single session of strain counterstrain manual therapy applied to latent myofascial trigger points of the upper trapezius muscle.
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Strain counterstrain is an indirect manual therapy technique in which the body is passively positioned in a pain-free posture to reduce nociceptive input and muscle tension.
In this study, a single session of strain counterstrain was applied to latent myofascial trigger points of the upper trapezius muscle.
|
|
Experimental: Fascial Distortion Model Group
Participants received a single session of fascial distortion model manual therapy applied to latent myofascial trigger points of the upper trapezius muscle.
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The fascial distortion model is a direct manual therapy approach that applies localized, high-intensity pressure to specific fascial distortions identified through patient body language and palpation.
In this study, a single session of fascial distortion model intervention was applied to latent myofascial trigger points of the upper trapezius muscle.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical Range of Motion
Time Frame: Before and immediately after the intervention
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Active cervical range of motion was measured using a Cervical Range of Motion (CROM) device in flexion, extension, lateral flexion, and rotation.
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Before and immediately after the intervention
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Pressure Pain Threshold
Time Frame: Before and immediately after the intervention
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Pressure pain threshold at the latent myofascial trigger point of the upper trapezius muscle was measured using a digital algometer.
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Before and immediately after the intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cervical Proprioception
Time Frame: Before and immediately after the intervention
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Cervical proprioception was assessed using joint position error during cervical lateral flexion measured with a CROM device.
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Before and immediately after the intervention
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Cervical Muscle Strength
Time Frame: Before and immediately after the intervention
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Isometric cervical muscle strength was measured using a digital muscle tester during flexion, extension, lateral flexion, and rotation.
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Before and immediately after the intervention
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: JiYoung Kim, PT, PhD, Kyungnam University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Other Study ID Numbers
- JYK-2025-02
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
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