NCT06910332

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
48

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 28, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 4, 2025

Completed
27 days until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2025

Completed
5 months until next milestone

Results Posted

Study results publicly available

December 9, 2025

Completed
Last Updated

December 9, 2025

Status Verified

July 1, 2025

Enrollment Period

2 months

First QC Date

March 28, 2025

Results QC Date

July 7, 2025

Last Update Submit

November 18, 2025

Conditions

Keywords

mobilizationproprioceptionstrengthshoulder

Outcome Measures

Primary Outcomes (2)

  • Proprioception

    Laser pointer-assisted joint position reproduction test for shoulder: A laser pointer is strapped 5 cm above the lateral epicondyle. Participants actively move their arm to a predefined position (90° flexion or abduction), and the laser projection is marked. After lowering their arm and closing their eyes, they attempt to replicate the same position. The difference between the initial and reproduced positions (in millimeters) is measured

    Before the intervention

  • Proprioception

    Laser pointer-assisted joint position reproduction test for shoulder: A laser pointer is strapped 5 cm above the lateral epicondyle. Participants actively move their arm to a predefined position (90° flexion or abduction), and the laser projection is marked. After lowering their arm and closing their eyes, they attempt to replicate the same position. The difference between the initial and reproduced positions (in millimeters) is measured

    Immediately after intervention

Secondary Outcomes (2)

  • Muscle Strength

    Before the intervention

  • Muscle Strength

    Immediately after intervention

Study Arms (2)

Mobilization Group

EXPERIMENTAL

Participants receive passive shoulder joint mobilization targeting the glenohumeral joint.

Other: Joint mobilization

Sham Group

SHAM COMPARATOR

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

Other: Sham

Interventions

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.

Also known as: Shoulder joint mobilization, Shoulder joint glides
Mobilization Group
ShamOTHER

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.

Also known as: Sham mobilization, Sham shoulder mobilization
Sham Group

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Healthy university students aged 18-25 years.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Acıbadem University Kerem Aydınlar Campus

Ataşehir, Istanbul, 34752, Turkey (Türkiye)

Location

MeSH Terms

Interventions

salicylhydroxamic acid

Results Point of Contact

Title
Ali Ömer ACAR
Organization
Acıbadem University, Department of Physiotherapy and Rehabilitation

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: 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.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 28, 2025

First Posted

April 4, 2025

Study Start

May 1, 2025

Primary Completion

June 30, 2025

Study Completion

June 30, 2025

Last Updated

December 9, 2025

Results First Posted

December 9, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will share

Demographic Data: Age and gender, Outcome Measures Data: Muscle strength values recorded using the hand-held dynamometer for each muscle group (shoulder flexors, abductors, internal rotators, external rotators). Proprioception data measured by the laser pointer-assisted joint position reproduction test, including the distance (in millimeters) between the initial and reproduced positions for both shoulder flexion and abduction. Group Assignment Data: Whether the participant was assigned to the mobilization group or the sham intervention group. Intervention Data: Details of the intervention received, including whether they underwent shoulder mobilization or placebo procedure. Timing of Measurements: Pre- and post-intervention data for both muscle strength and proprioception assessments.

Shared Documents
STUDY PROTOCOL, ICF
Time Frame
The IPD and supporting information will be made available starting from the date of publication of the study's results. The data will be accessible for 5 years from the publication date to allow for ample time for further analysis, replication studies, or meta-analysis by other researchers.
Access Criteria
Who Can Access: * Researchers, academics, and institutional partners with a legitimate research purpose. * Regulatory agencies or health organizations. What They Can Access: * Anonymized IPD (muscle strength, proprioception, demographics). * Supporting information (study protocol, SAP,) How They Can Access: * Data will be shared upon contact with the study team. * Interested parties must request access, and data will be provided following review and approval.

Locations