Effectiveness of a Novel Protocol for Glenohumeral Internal Rotation Deficit in General Population With Shoulder Pain

NCT ID: NCT05108311

Last Updated: 2023-07-14

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-10-22

Study Completion Date

2022-01-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Shoulder pain is one of the most common joint problems and disabling complaint in general population., but there is a lack of evidence about the relation between shoulder pain and glenohumeral internal rotation deficit (GIRD) in general population.

This study aimed to determine if the novel proposal for treatment of GIRD could be effectiveness and gain further evidence in the Range of Motion an Pain.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Shoulder Pain Glenohumeral Internal Rotation Deficit

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Treatment

The Treatment sequence including joint Manual therapy techniques and soft tissue release techniques is proposed.

Group Type EXPERIMENTAL

Manual therapy and therapeutic exercise

Intervention Type OTHER

1. Gliding over the deltoid superficial fascia.
2. Anterior-Posterior mobilization of the clavicle.
3. myofascial release of the shoulder joint complex techniques.
4. Myofascial release external rotation with glenohumeral decoaptation will be carry out in prone position facility the triangular space, quadrangular space and triceps hiatus.
5. anterior and posterior, superior and inferior glenohumeral inferior glide mobilization in adduction will perform in a prone position to facilitate glenohumeral re centration.
6. scapular musculature myofascial release including mobilization with a scapulothoracic joint decoaptation, and angular of the scapula.
7. Supine mobilization of the posterior capsule in 90º shoulder flexion and the adduction.

Finally the patient will be instructed to adapt the daily active biological stimulus at home to maximize the benefits of the manual therapy

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Manual therapy and therapeutic exercise

1. Gliding over the deltoid superficial fascia.
2. Anterior-Posterior mobilization of the clavicle.
3. myofascial release of the shoulder joint complex techniques.
4. Myofascial release external rotation with glenohumeral decoaptation will be carry out in prone position facility the triangular space, quadrangular space and triceps hiatus.
5. anterior and posterior, superior and inferior glenohumeral inferior glide mobilization in adduction will perform in a prone position to facilitate glenohumeral re centration.
6. scapular musculature myofascial release including mobilization with a scapulothoracic joint decoaptation, and angular of the scapula.
7. Supine mobilization of the posterior capsule in 90º shoulder flexion and the adduction.

Finally the patient will be instructed to adapt the daily active biological stimulus at home to maximize the benefits of the manual therapy

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Shoulder pain

Exclusion Criteria

* Patient under 18 years old,
* Pain in both shoulders
* Joint prosthesis in at least one of the two shoulders.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

CEU San Pablo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Rafael Jácome López, PT

Role: PRINCIPAL_INVESTIGATOR

Clínica Universidad de Navarra

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

San Pablo CEU University

Boadilla del Monte, Madrid, Spain

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Spain

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CEU-024

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.