The Effect of Isolytic and Static Stretching Training in Individuals With Subacromial Impingement Syndrome

NCT ID: NCT03246698

Last Updated: 2022-07-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-08-28

Study Completion Date

2019-07-20

Brief Summary

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The purpose of this study is to investigate and compare the effect of isolytic and static stretching training in individuals having subacromial impingement syndrome with glenohumeral internal rotation deficit. Isolytic group will receive isolytic stretching in modified cross body stretching position and standard physiotherapy program. Static group will receive static stretching in modified cross body stretching position and standard physiotherapy program. Control group will receive only standard physiotherapy program.

Detailed Description

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The effectiveness of static stretching on various parameters such as range of motion or pain is studied and proved in literature. Static stretching in cross body position was also found helpful for improving shoulder range of motion with some disadvantages. In modified cross body position, the patient is positioned in a more advantageous way for him/her. Usually this stretching is done as active-assistive static stretching with the physiotherapist. Proof is still needed for the effectiveness of active-assistive static stretching in modified cross body position. Furthermore, there is no research about the effect of isolytic stretching which is relatively new technique compare to static stretches in subacromial impingement syndrome. In isolytic stretching, when the patient contracts the agonist muscle group with 20% muscle force active-assistive streching in agonist muscle group by the physiotherapist at the same time is done for 2-4 seconds. A fast isolytic stretching is applied in order to break the fibrous tissue. Our purpose is to investigate and compare the effect of isolytic and static stretching training in individuals having subacromial impingement syndrome with glenohumeral internal rotation deficit . Stretching groups will receive either isolytic or static stretching in modified cross body stretching position and standard physiotherapy program. There is a control group. Control group will receive only standard physiotherapy program. Standard physiotherapy program includes TENS, hotpack, posture and strengthening training program. Treatment program will last four times a week (4-4-4-3) for four weeks, 15 sessions in total.

Conditions

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Subacromial Impingement Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

There are 3 groups. First group will receive isolytic stretching in modified cross body stretching position and standard physiotherapy program. Second group will receive static stretching in modified cross body stretching position and standard physiotherapy program. Control group will receive only standard physiotherapy program. In standard physiotherapy program, there are TENS, hotpack, posture and strengthening training program. Treatment program will last four weeks.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
All of participants must have subacromial impingement syndrome with glenohumeral internal rotation deficit.

Study Groups

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Isolytic stretching group

The participants in this group will receive isolytic stretching in modified cross body position. Additionally they will receive standard physiotherapy.

Group Type EXPERIMENTAL

Isolytic Stretching group

Intervention Type OTHER

In modified cross body position, isolytic stretching exercises will perform five times each for 15 seconds. After each stretching patient will rest for 5 seconds. When the patient contracts the agonist muscle group with 20% muscle force, the agonist muscle group is stretched at the same time for 2-4 seconds. Isolytic stretching exercises will perform four times a week for four weeks. It's obligatory to receive at least 15 sessions in total. They will also receive standard physiotherapy program four times a week for four week, 15 sessions in total.

Static stretching group

The participants in this group will receive static stretching in modified cross body position.

Additionally they will receive standard physiotherapy.

Group Type EXPERIMENTAL

Static Stretching group

Intervention Type OTHER

In modified cross body position, active-assistive static stretching exercises will be performed 5 times each for 15 seconds. This stretching exercise is performed 5 times with 5 seconds intervals. Static stretching exercises will perform four times a week for four weeks. It's obligatory to receive at least 15 sessions in total. They will also receive standard physiotherapy program four times a week for four week, 15 sessions in total.

Control group

The participants in this group will receive only standard physiotherapy.

Group Type ACTIVE_COMPARATOR

Control group

Intervention Type OTHER

They will receive only standard physiotherapy program, four times a week for four weeks, 15 sessions in total.

Interventions

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Isolytic Stretching group

In modified cross body position, isolytic stretching exercises will perform five times each for 15 seconds. After each stretching patient will rest for 5 seconds. When the patient contracts the agonist muscle group with 20% muscle force, the agonist muscle group is stretched at the same time for 2-4 seconds. Isolytic stretching exercises will perform four times a week for four weeks. It's obligatory to receive at least 15 sessions in total. They will also receive standard physiotherapy program four times a week for four week, 15 sessions in total.

Intervention Type OTHER

Static Stretching group

In modified cross body position, active-assistive static stretching exercises will be performed 5 times each for 15 seconds. This stretching exercise is performed 5 times with 5 seconds intervals. Static stretching exercises will perform four times a week for four weeks. It's obligatory to receive at least 15 sessions in total. They will also receive standard physiotherapy program four times a week for four week, 15 sessions in total.

Intervention Type OTHER

Control group

They will receive only standard physiotherapy program, four times a week for four weeks, 15 sessions in total.

Intervention Type OTHER

Other Intervention Names

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Standard physiotherapy Standard physiotherapy Standard physiotherapy

Eligibility Criteria

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Inclusion Criteria

* Diagnosis of subacromial impingement syndrome
* Glenohumeral internal rotation range of motion of the affected shoulder should be less than other shoulder and bilateral shoulder internal rotation range of motion difference should be ≥15 º
* Pain with resisted arm elevation or external rotation as well as a minimum of 3 of 5 positive subacromial impingement syndrome tests, painful arc, pain or weakness with resisted external rotation, Neer, Hawkins and Jobe tests.
* Ability to complete the entire study procedure

Exclusion Criteria

* A 50% limitation of passive shoulder range of motion in \>2 planes of motion
* Pain \>7/10
* A history of fracture to the shoulder girdle
* Systemic musculoskeletal disease
* History of shoulder and cervical surgery
* Glenohumeral instability (positive apprehension, relocation, or positive sulcus test) or positive findings for a full-thickness rotator cuff tear (positive lag sign, positive drop arm test, or marked weakness with shoulder external rotation)
* Neck and shoulder pain with active/passive cervical spine movement
* A diagnosis of chest deformity or scoliosis
* Regularly performing posterior shoulder stretching exercises
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Dokuz Eylul University

OTHER

Sponsor Role lead

Responsible Party

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Halime Ezgi TÜRKSAN

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sevgi Sevi YESILYAPRAK, PhD

Role: STUDY_DIRECTOR

Dokuz Eylul University

Mehmet ERDURAN, MD

Role: STUDY_DIRECTOR

Dokuz Eylul University

Cem OZCAN, MD

Role: STUDY_DIRECTOR

Izmır Katip Celebi University Atatürk Training and Research Hospital

Locations

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Dokuz Eylül University

Izmir, Balçova, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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3413-GOA

Identifier Type: -

Identifier Source: org_study_id

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