Instrument-assisted Soft Tissue Mobilization in CrossFitters

Not Applicable

• Conditions: Sports Physical Therapy
• Interventions: Other: Instrument-assisted

• Registration Number: NCT03830346
• Lead Sponsor: Real Fundación Victoria Eugenia

Brief Summary

Objective. To determine the effectiveness of instrument assisted soft tissue mobilization and horizontal adduction stretch in CrossFit practitioners' shoulders.

Setting: Acero CrossFit center, city of Toledo (Spain) Design: Randomized, single-blind pilot study, with follow-up period. Participants: Twenty-one subjects of both sexes, being regular CrossFitters and in the age range of 18 to 40 years.

Intervention: The experimental group (n = 11) received 30 seconds of stretching with isometric contraction of 5 seconds and instrument assisted soft tissue mobilization. The control group (n = 10) received only 40 seconds of instrument assisted soft tissue mobilization. Each session lasted 2 to 5 minutes, 2 days a week, over a period of 4 weeks, prior to each workout.

Main Outcome measures: Shoulder internal rotation and horizontal adduction (digital inclinometer), and posterior shoulder stretch perception (Park scale) were evaluated.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-01-31
• Status Verified: 2019-02
• Study Start: 2019-02-01
• Study First Submitted QC: 2019-02-01
• Last Update Submitted: 2019-02-01
• Study First Posted: 2019-02-05
• Last Update Posted: 2019-02-05
• Primary Completion: 2019-06-01
• Study Completion: 2019-07-01

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 21

Inclusion Criteria

• Subjects of both sexes
• Being regular CrossFitters (workouts at least two days a week)
• In the age range of 18 to 40 years

Exclusion Criteria

• Had suffered a shoulder injury in the 3 months prior to the study
• Had undergone shoulder surgery in the previous six months
• Had a non-attendance rate of over 15% of the intervention sessions (2 sessions)
• Had not signed the informed consent document

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Control	Instrument-assisted	Control group only underwent soft tissue mobilization. With the subject in the supine position, passively adducting the arm horizontally until the first motion barrier and performing active horizontal abduction for 5 seconds at 25% of force. The arm was then taken to the new motion barrier, repeating this process three times.
Experimental	Instrument-assisted	In the experimental group, instrument-assisted soft tissue mobilization techniques and post-isometric horizontal adduction stretches were performed. The technique lasted 20 seconds in a parallel direction and 20 seconds in a perpendicular direction on the posterior shoulder and scapula muscles. While the dominant hand was used to hold the instrument, the other hand was used to tighten the skin medially to ensure an even area of treatment.

Primary Outcome Measures

Name	Time	Method
Change from baseline internal rotation and horizontal adduction of the shoulder after treatment and at 1 month	Screening visit, within the first seven days after treatment and after one month follow-up visit	The patient was placed in the supine position at 90º shoulder abduction, 90º elbow flexion. By stabilizing the scapula at the acromion, the shoulder was taken at a maximum range of internal rotation. The range of motion was measured with a digital inclinometer, model Tacklife MDP01, the angle of the edge of the ulna coinciding with a line perpendicular to the stretcher. For horizontal adduction, the arm was placed in the same initial position in neutral rotation and while stabilizing the lateral edge of the scapula, the arm was adducted to its maximum range of motion. The angle between the line of the ventral edge of the humerus and a line perpendicular to the stretcher was measured with the inclinometer. The range of movement in internal rotation is 0-70º and the range in horizontal adduction is 0-30º (higher degrees, greater mobility in horizontal adduction of the shoulder).

Secondary Outcome Measures

Name	Time	Method
Change from baseline perception of stretch after treatment and at 1 month	Screening visit, within the first seven days after treatment and after one month follow-up visit	An 11-point numerical rating scale was used to rate subjects' perceptions of discomfort at the posterior aspect of the shoulder. This 11-point scale evaluates the discomfort from least to most, asking each subject to define the level of discomfort in the back of the shoulder in the maximum range of motion of internal rotation and horizontal adduction of the shoulder. This 11-point scale measures the perception of stretching, in a range of 0 to 10 points ("0" on the stretch sensation scale indicated ''no discomfort'' and "10" indicated ''the worst possible discomfort and increased sensitivity')

Trial Locations

Locations (1)

Real Fundación Victoria Eugenia; 🇪🇸 Madrid, Spain