NCT07368426

Brief Summary

This pilot study aimed to compare the immediate effects of two manual therapy techniques, strain counterstrain (SCS) and the fascial distortion model (FDM), on pain-related outcomes and neuromuscular function in individuals with latent myofascial trigger points of the upper trapezius muscle. Twenty healthy adults with identified latent trigger points were randomly assigned to receive a single session of either SCS or FDM. Cervical range of motion, proprioception, pressure pain threshold, and cervical muscle strength were assessed before and immediately after the intervention. This study was conducted to obtain preliminary data regarding the short-term effects of two manual therapy approaches with contrasting stimulation characteristics.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

January 18, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 26, 2026

Completed
Last Updated

January 26, 2026

Status Verified

January 1, 2026

Enrollment Period

2 months

First QC Date

January 18, 2026

Last Update Submit

January 18, 2026

Conditions

Keywords

Strain CounterstrainFascial Distortion ModelManual TherapyMyofascial Trigger PointUpper Trapezius

Outcome Measures

Primary Outcomes (2)

  • Cervical Range of Motion

    Active cervical range of motion was measured using a Cervical Range of Motion (CROM) device in flexion, extension, lateral flexion, and rotation.

    Before and immediately after the intervention

  • Pressure Pain Threshold

    Pressure pain threshold at the latent myofascial trigger point of the upper trapezius muscle was measured using a digital algometer.

    Before and immediately after the intervention

Secondary Outcomes (2)

  • Cervical Proprioception

    Before and immediately after the intervention

  • Cervical Muscle Strength

    Before and immediately after the intervention

Study Arms (2)

Strain Counterstrain Group

EXPERIMENTAL

Participants received a single session of strain counterstrain manual therapy applied to latent myofascial trigger points of the upper trapezius muscle.

Other: Strain Counterstrain

Fascial Distortion Model Group

EXPERIMENTAL

Participants received a single session of fascial distortion model manual therapy applied to latent myofascial trigger points of the upper trapezius muscle.

Other: Fascial Distortion Model

Interventions

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.

Strain Counterstrain Group

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.

Fascial Distortion Model Group

Eligibility Criteria

Age18 Years - 39 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kyungnam University

Changwon, Gyeongsangnam-do, 51767, South Korea

Location

Study Officials

  • JiYoung Kim, PT, PhD

    Kyungnam University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Adjunct Professor, Physical Therapy

Study Record Dates

First Submitted

January 18, 2026

First Posted

January 26, 2026

Study Start

September 1, 2025

Primary Completion

October 31, 2025

Study Completion

October 31, 2025

Last Updated

January 26, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations