The Effect of Shoulder Mobilization on Muscle Strength and Proprioception: a Randomized Double-blind Study

NCT ID: NCT06910332

Last Updated: 2025-12-09

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

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

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-05-01

Study Completion Date

2025-06-30

Brief Summary

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

This randomized, double-blind study examines the acute effects of shoulder mobilization on muscle strength and proprioception in healthy individuals. Forty-eight participants (aged 18-25) were randomly assigned to either a mobilization or sham intervention group. Muscle strength and proprioception were assessed before and after treatment. The mobilization group received passive shoulder joint glides, while the sham group underwent a placebo procedure. The study aims to determine whether mobilization affects strength and proprioception immediately.

Detailed Description

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

Summary of the Study

This randomized, double-blind study investigates the acute effects of shoulder joint mobilization on muscle strength and proprioception in healthy individuals compared to a sham intervention.

Background:

The shoulder joint is highly mobile and prone to injury, with rehabilitation often including manual therapy techniques like joint mobilization. Mobilization may enhance joint stability, neuromuscular control, and proprioception by stimulating mechanoreceptors. However, its immediate effects on shoulder proprioception and strength remain unclear.

Methods:

Participants: 48 healthy university students (aged 18-25) randomly assigned to either the mobilization or sham group.

Assessments: Muscle strength (using a handheld dynamometer) and proprioception (laser pointer-assisted joint position reproduction test) were measured before and after the intervention.

Intervention: The mobilization group received passive shoulder joint glides, while the sham group underwent a placebo procedure without actual joint movement.

Conclusion:

This study aims to determine whether shoulder mobilization has immediate effects on proprioception and strength.

Conditions

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

Healthy Male and Female Subjects

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

Participants are randomly assigned to either the shoulder mobilization group or the sham mobilization group, and they remain in their assigned group throughout the study. This design allows for a direct comparison of the acute effects of mobilization on muscle strength and proprioception.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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

Mobilization Group

Participants receive passive shoulder joint mobilization targeting the glenohumeral joint.

Group Type EXPERIMENTAL

Joint mobilization

Intervention Type OTHER

Participants receive passive shoulder joint mobilization on the dominant-side glenohumeral joint. The mobilization includes inferior, anterior, and posterior glide techniques, each performed for 1 minute at a frequency of 0.5 Hz, with a 30-second rest between each mobilization. The participant is positioned comfortably to support the joint's range of motion.

Sham Group

Participants undergo a placebo procedure where the practitioner mimics the mobilization technique without applying actual joint movement or distraction.

Group Type SHAM_COMPARATOR

Sham

Intervention Type OTHER

In the sham intervention, the practitioner mimics the technique of shoulder mobilization but does not apply any actual movement or glide effect on the joint. The procedure is designed to closely resemble the real intervention in terms of duration, rhythm, and the practitioner's handling of the participant's shoulder. The practitioner will use superficial touch on the glenohumeral joint without applying any of the mobilizing forces necessary to move the joint.

Interventions

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

Joint mobilization

Participants receive passive shoulder joint mobilization on the dominant-side glenohumeral joint. The mobilization includes inferior, anterior, and posterior glide techniques, each performed for 1 minute at a frequency of 0.5 Hz, with a 30-second rest between each mobilization. The participant is positioned comfortably to support the joint's range of motion.

Intervention Type OTHER

Sham

In the sham intervention, the practitioner mimics the technique of shoulder mobilization but does not apply any actual movement or glide effect on the joint. The procedure is designed to closely resemble the real intervention in terms of duration, rhythm, and the practitioner's handling of the participant's shoulder. The practitioner will use superficial touch on the glenohumeral joint without applying any of the mobilizing forces necessary to move the joint.

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Shoulder joint mobilization Shoulder joint glides Sham mobilization Sham shoulder mobilization

Eligibility Criteria

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

Inclusion Criteria

* Healthy university students aged 18-25 years.

Exclusion Criteria

* Individuals with orthopedic problems in the shoulder complex.
* Those who have undergone previous shoulder surgery.
* Participants with prior knowledge of joint mobilization techniques that could affect the sham intervention.
Minimum Eligible Age

18 Years

Maximum Eligible Age

25 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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

Acibadem 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

Locations

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

Acıbadem University Kerem Aydınlar Campus

Ataşehir, Istanbul, Turkey (Türkiye)

Site Status

Countries

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

Turkey (Türkiye)

Provided Documents

Download supplemental materials such as informed consent forms, study protocols, or participant manuals.

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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

ACU-FTR-AOA

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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