Skip to content

Myofascial Release of the Pectoral Fascia

Myofascial Release of the Pectoral Fascia: Effect on Shoulder Posture, Muscle Length, Muscle Activity, and Movement Performance

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04944745
Acronym
MTRF
Enrollment
60
Registered
2021-06-30
Start date
2020-10-14
Completion date
2021-11-06
Last updated
2022-03-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Brief summary

Neck-shoulder pain is among the most common health care problems, especially in office workers and females. Forward shoulder posture (FSP) is a common postural deviation and known risk factor for the development of neck-shoulder pain and pathology. Common approaches for reducing FSP include stretching and performing manual techniques to increase the length and extensibility of the scapular protractors, and strengthening the scapular retractors. Myofascial release (MFR) is a group of manual techniques that elongate and soften restricted fascia, however, the effects of myofascial release to the pectorals on FSP are currently unknown. The objectives of this study are to determine the impact of 4-minutes of MFR on: 1) FSP, 2) pectoral length, 3) muscle activity of the upper, middle, and lower trapezius and pectoralis major, 4) scapular retractor to protractor ratio of activity, and 4) movement performance compared to a soft-touch control. We hypothesize that MFR will: 1) decrease FSP, 2) increase pectoral length, 3) increase upper, middle, and lower trapezius activity and decrease pectorals major activity, 4) increase the scapular retractor to protractor ratio of activity, and 4) improve movement performance.

Interventions

OTHERMyofascial Release

Moderate pressure manual treatment to the pectoral fascia.

OTHERSoft-touch Control

No pressure manual treatment to the pectoral fascia.

Sponsors

Centennial College
CollaboratorOTHER
University of Manitoba
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

The participants will have knowledge of the two different intensity treatments they will receive. However, the researchers will be blinded as to which treatment intensity the participant received at which session.

Intervention model description

Single blind between subjects repeated measures crossover design

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* have 1 cm of anterior deviation of the acromion process (forward shoulder posture) * right handed

Exclusion criteria

* recent history (\<6 months) of neck, shoulder, or upper back pain * recent history (\<6 months) of neck, shoulder, or upper back injury/pathology * history of orthopaedic or neurological disorders

Design outcomes

Primary

MeasureTime frameDescription
Change in Forward shoulder posture after intervention30-minutesRelative- photographic analysis. Participant stand in a relaxed position and have a photo taken from their side where an online program will be used to quantify their forward shoulder posture
Change in Pectoral Length after intervention30-minutesMeasured passive horizontal abduction of the shoulder
Change in Muscle Activity- Upper Trapezius after intervention30-minutessEMG during a reaching task
Change in Muscle Activity- Middle Trapezius after intervention30-minutessEMG during a reaching task
Change in Muscle Activity- Lower Trapezius after intervention30-minutessEMG during a reaching task
Change in Muscle Activity- Pectoralis Major after intervention30-minutessEMG during a reaching task
Change in Movement performance- reaction time after intervention30-minutesParticipants will complete a reaching task using custom designed software (E-Prime). The reaching task is a modified Fitts' Task where the participant must reach towards one of five randomly appearing targets.
Change in Movement performance- movement time after intervention30-minutesParticipants will complete a reaching task using custom designed software (E-Prime). The reaching task is a modified Fitts' Task where the participant must reach towards one of five randomly appearing targets.
Change in Movement performance- accuracy after intervention30-minutesParticipants will complete a reaching task using custom designed software (E-Prime). The reaching task is a modified Fitts' Task where the participant must reach towards one of five randomly appearing targets.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026