Effects of Neuromuscular Taping on Shoulder Pain and Function in Pitchers: A Clinical Trial

NCT ID: NCT07316946

Last Updated: 2026-01-05

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

62 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-02-13

Study Completion Date

2026-07-30

Brief Summary

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

Effects of Neuromuscular Taping on Shoulder Pain and Function in Pitchers: A Clinical Trial

Detailed Description

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

Randomized clinical trial 2 arms

Conditions

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

Shoulder Pain

Study Design

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

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized clinical trial 2 arms
Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Outcome Assessors
participants and outcome assessors will be blinded

Study Groups

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

Placebo group

The placebo group will receive the same bandage, with the same strip arrangement, but without any tension (0%) applied to any of the strips. Furthermore, participants will not receive any instructions for muscle activation during application. This placebo technique has been used in previous studies, supporting its methodological validity.

Group Type PLACEBO_COMPARATOR

Placebo Group

Intervention Type OTHER

The placebo group will receive the same taping, with an identical arrangement of the strips, but without applying any tension (0%) to them. In addition, participants will not receive any instructions regarding muscle activation during the application. This placebo taping model has been used in previous studies, supporting its methodological validity.

Experimental group

The experimental group will receive neuromuscular taping with kinesiology tape, consisting of two longitudinal strips applied along the lower trapezius muscle, with a tension close to 100% of the tape's elastic capacity. During application, the participant will be asked to activate the scapular depressor and retractor muscles.

Additionally, two more longitudinal strips will be applied from the anterior portion of the humeral head towards the scapular spine, also with a tension close to 100%. During this application, the participant will be asked to activate the rotator cuff by applying a posteroanterior push to the humeral head.

Group Type EXPERIMENTAL

Experimental Group

Intervention Type OTHER

The experimental group will receive a multilayer neuromuscular taping application using kinesiotape, consisting of the placement of two longitudinal strips in the direction of the lower trapezius, applied with tension close to 100% of the tape's elastic capacity. During the application, participants will be asked to activate the scapular depressor and retractor muscles.

Additionally, two other longitudinal strips will be applied from the anterior portion of the humeral head toward the scapular spine, also with tension close to 100%. During this application, participants will be asked to activate the rotator cuff through a posteroanterior push of the humeral head.

Interventions

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

Experimental Group

The experimental group will receive a multilayer neuromuscular taping application using kinesiotape, consisting of the placement of two longitudinal strips in the direction of the lower trapezius, applied with tension close to 100% of the tape's elastic capacity. During the application, participants will be asked to activate the scapular depressor and retractor muscles.

Additionally, two other longitudinal strips will be applied from the anterior portion of the humeral head toward the scapular spine, also with tension close to 100%. During this application, participants will be asked to activate the rotator cuff through a posteroanterior push of the humeral head.

Intervention Type OTHER

Placebo Group

The placebo group will receive the same taping, with an identical arrangement of the strips, but without applying any tension (0%) to them. In addition, participants will not receive any instructions regarding muscle activation during the application. This placebo taping model has been used in previous studies, supporting its methodological validity.

Intervention Type OTHER

Eligibility Criteria

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

Inclusion Criteria

* age over 18 years
* compete in a sport that involves overhead movement patterns
* train at least 2 hours per week
* shoulder pain lasting more than six weeks
* shoulder pain related to sports activity
* understand Spanish fluently enough to complete the questionnaire assessment.

Exclusion Criteria

* presence of red flags that could suggest fractures, dislocations, or complete tendon ruptures, among others
* neurological pathologies
* other severe pathologies such as inflammatory arthritis, frozen shoulder
* having received corticosteroid injections or physiotherapy treatment in the last six months
* presence of previous surgeries
* pregnancy
* cognitive deficits that could limit the comprehension of the questionnaires or the physical evaluation
* skin problems that would be a contraindication for any type of bandage.
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.

Sandra Jiménez-del-Barrio

OTHER

Sponsor Role lead

Responsible Party

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

Sandra Jiménez-del-Barrio

PhD Physiotherapist

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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

Faculty of Health Sciences

Soria, Soria, Spain

Site Status

Countries

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

Spain

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Sandra Jiménez del Barrio, Phd

Role: primary

975129166

Other Identifiers

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

REF CEIm

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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