Fascial Manipulation Effect on Shoulder Range of Motion and Strength in Handball Players

August 22, 2023 updated by: Anja Baric

The Effect of Fascial Manipulation Technique by Stecco on the Shoulder Range of Motion and External Rotation Strength of Asymptomatic Handball Players

The investigators conducted a prospective randomized controlled trial on the female and male handball players from the Izola Handball Club (Slovenia) who volunteered to participate in the study. Data were collected in the first part of the competition season 2022/2023. The participants were randomly divided into investigated and control groups so that each group had approximately the same number of participants regarding sex and age. The Fascial manipulation (FM) was performed in the investigated group, whereas, in the control group, the participants did not receive the FM. Demographics (sex, age, height, weight, throwing shoulder, playing position, years of playing) were collected. The study protocol complied with the Declaration of Helsinki and was approved by the National Medical Ethics Committee of the Republic of Slovenia (0120-78/2022/9).

The aim of this research was to determine whether and how FM affects IR, HADD ROM and the strength of ER in handball players. The hypotheses include: (1) an increase in IR, HADD ROM, and strength of ER immediately after FM compared to the control group, (2) maintenance of increased ROM and ER strength one month after FM compared to baseline and the control group, (3) a decrease in the subjective feeling of tightness immediately and one month after and (4) the size of the FM effect increases with years of playing and vice versa.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

All participants aged 18 or older signed informed consent to participate in the study. For participants under 18 years of age, informed consent was signed by their parents or legal guardians. Exclusion criteria were prior upper extremity injury or upper extremity surgery preventing the player from playing in the last three months, any previous shoulder surgery, and goalkeeper position. A cluster random sampling strategy was used. The participants were randomly divided into investigated and control groups so that each group had approximately the same number of units regarding sex and age. In the investigated group, the Fascial manipulation (FM) was performed, whereas, in the control group, the participants did not receive the FM.

One session of Fascial Manipulation® by Stecco was chosen as the therapeutic procedure. The principal investigator who performed the FM in the investigated group is a qualified therapist with extensive knowledge in manual therapy and a certificate in FM Levels I and II. Based on the collected information (a complete medical history, including the chronology of any traumatic events, fractures, significant musculoskeletal dysfunctions, scars and surgical procedures, specific range of motion, and palpation examinations) and according to the Stecco model for the interpretation of the dysfunction of the fascial system, the therapist selected an individual combination of condensed points of treatment (centers of coordination - CC and/or centers of fusion - CF). All CC and/or CF points that were treated in an individual subject were recorded.

All participants completed three test sessions (pre-test, immediate post-test, and one-month post-test). The immediate post-test measurements were recorded directly after the application of the FM in the investigated group and after a one-minute waiting period in the control group. Testing was repeated 27-34 days (one month) after FM was performed. All three measurements for both groups were performed in the same way. All the measurements were performed by the two independent examiners - experienced physical therapists, whereby FM was performed only by the principal investigator-experienced physical therapist who did not participate in the measurements. Before the measurements, participants completed a specific standard warm-up for their team consisting of gentle jogging, static and dynamic full-body stretching. The warm-up was not standardized for this study.

Range of motion (ROM) measurements for internal rotation (IR) and horizontal adduction (HADD) were recorded using a classic goniometer. For the HADD assessment, participants were positioned supine on a standard examination table with both shoulders aligned. The examiner stood on top of the table, facing the participant's head, and stabilized the lateral edge of the scapula. The participant's upper limb was positioned at 90 degrees of GH abduction with 90 degrees of elbow flexion. The examiner held the subject's arm distal to the elbow and passively moved it into HADD. At the first point of resistance, a second examiner used a digital inclinometer to record the amount of motion in degrees (°) by aligning it with the humerus.

Passive IR measurements were taken with the participant lying supine on an examination table, with the shoulder at 90 degrees of abduction in the frontal plane and the elbow at 90 degrees of flexion. The examiner applied a posterior stabilizing force to the acromial process of the scapula and internally rotated the upper limb until the first point of resistance. A second investigator then recorded the amount of movement in degrees by aligning the digital inclinometer with the axis of the forearm.

The Easy Force© digital dynamometer was used to determine the strength of the external rotation (ER). Maximal isometric strength was measured in Newtons per kilogram (N/kg). Subjects lay prone, with the shoulder abducted to 90° in the frontal plane and in neutral rotation. The first examiner placed the dynamometer strap around the wrist, 2cm proximal to the ulnar styloid process. The tape on the other side of the dynamometer was fixed in a stand next to the table, in extension with the wrist. The second examiner fixed the humerus on the distal side just above the elbow to limit the motion of the humerus. According to standardized testing instructions, the procedure was as follows: one familiarization trial, then three maximal isometric tests. Participants were asked to gradually build up their strength to maximal effort over a two-second period and finally to hold their maximal effort for three seconds. The best measurement from three trials, expressed in N/kg, was used for analysis.

One session of Fascial Manipulation® by Stecco was chosen as the therapeutic procedure for the investigated group. The principal investigator who performed the FM is a qualified therapist with extensive knowledge in manual therapy and holds certificates in FM Levels I and II. The therapist utilized the Stecco model to interpret the dysfunction of the fascial system based on comprehensive information collected, including the participant's complete medical history, traumatic events, fractures, musculoskeletal dysfunctions, scars, surgical procedures, specific range of motion, and palpation examinations. Using this information, the therapist selected an individualized combination of condensed treatment points, known as centers of coordination (CC) and/or centers of fusion (CF). All CC and/or CF points treated in each individual subject were recorded for documentation purposes.

Study Type

Interventional

Enrollment (Actual)

56

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Izola, Slovenia, 6310
        • Izola Handball Club

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Asymptomatic and healthy handball players from Izola Handball Club (Slovenia)
  • Both male and female participants who volunteer for the study and belong to cadet, junior, and senior handball teams
  • All participants aged 18 years and older, provided informed consent to participate in the study, whereas participants under the age of 18 need their parents or guardians to sign the informed consent form on their behalf.

Exclusion Criteria:

  • A recent upper extremity injury or surgery that hinders the player's ability to participate in the game of handball for the past three months
  • Any history of previous shoulder surgery
  • The playing position of goalkeeper.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Investigated group with fascial manipulation
Participants in this group received one treatment of fascial manipulation by Stecco method
Fascial Manipulation (FM) is a method carefully developed by members of the Stecco family after many years of research. FM involves deep kneading of the muscle fascia at specific points called centers of coordination (CC) and centers of fusion (CF) along myofascial sequences, diagonals, and spirals. It has been proposed that the friction caused by manipulation creates localized heat and that, due to the thermosensitive characteristics of fascia, this heat facilitates the transition of hyaluronic acid within the extracellular matrix from a condensed state to a more fluid state, thus restoring the gliding properties of fascia.
No Intervention: Control group with no intervention
Participants in this group received no treatment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The immediate effect of Fascial Manipulation (FM) on the shoulder joint internal rotation (IR) and horizontal adduction (HADD) range of motion (ROM)
Time Frame: immediately after FM
Investigated the difference in the shoulder joint internal rotation (IR) and shoulder joint horizontal adduction (HADD) ROM before and immediately after FM in both groups. A classic goniometer was used to record ROM measurements for IR and HADD in degrees (°).
immediately after FM
The immediate effect of Fascial Manipulation (FM) on the shoulder joint external rotation (ER) strength
Time Frame: immediately after FM
Investigated the difference in the strength of ER before and immediately after FM in both groups. The Easy Force© digital dynamometer was used to determine the strength of the ER. Maximal isometric strength was measured in newtons per kilogram (N/kg).
immediately after FM

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The effect of Fascial Manipulation (FM) on the shoulder joint internal rotation (IR) and horizontal adduction (HADD) range of motion (ROM) one month after FM
Time Frame: 27-34 days (one month)
Investigated the difference in values of internal rotation (IR) and horizontal adduction (HADD) range of motion (ROM) one month after FM in both groups. A classic goniometer was used to record ROM measurements for IR and HADD in degrees (°).
27-34 days (one month)
The effect of Fascial Manipulation (FM) on the shoulder joint external rotation (ER) strength one month after FM
Time Frame: 27-34 days (one month)
Investigated the difference in values of ER strength one month after FM in both groups. The Easy Force© digital dynamometer was used to determine the strength of the ER. Maximal isometric strength was measured in newtons per kilogram (N/kg).
27-34 days (one month)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2022

Primary Completion (Actual)

October 15, 2022

Study Completion (Actual)

October 15, 2022

Study Registration Dates

First Submitted

August 9, 2023

First Submitted That Met QC Criteria

August 22, 2023

First Posted (Actual)

August 24, 2023

Study Record Updates

Last Update Posted (Actual)

August 24, 2023

Last Update Submitted That Met QC Criteria

August 22, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • FM2223

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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