NCT07309796

Brief Summary

Postoperative rehabilitation after reverse shoulder arthroplasty aims to improve pain control, range of motion, and functional capacity. However, studies examining the effects of strengthening exercises targeting the humeral head depressor muscles are limited. This randomized controlled trial will evaluate the effects of adding a specific strengthening program to standard rehabilitation on pain, range of motion, quality of life, and functional outcomes.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
27

participants targeted

Target at below P25 for not_applicable

Timeline
7mo left

Started Jan 2026

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress38%
Jan 2026Dec 2026

First Submitted

Initial submission to the registry

December 15, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

December 30, 2025

Completed
3 days until next milestone

Study Start

First participant enrolled

January 2, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 2, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 2, 2026

Last Updated

March 3, 2026

Status Verified

March 1, 2026

Enrollment Period

8 months

First QC Date

December 15, 2025

Last Update Submit

March 2, 2026

Conditions

Keywords

Reverse shoulder arthroplastyDepressor muscle training. ShoulderArthroplasty

Outcome Measures

Primary Outcomes (3)

  • Pain Intensity (Visual Analog Scale - VAS)

    Pain intensity will be assessed using the Visual Analog Scale, a 10-cm line ranging from "no pain" to "worst imaginable pain." The distance from the "no pain" anchor to the participant's mark will be measured in millimeters (0-100 mm), with higher scores indicating higher pain intensity.

    6 weeks

  • Upper Extremity Disability (Disabilities of the Arm, Shoulder and Hand Questionnaire - DASH)

    The DASH is a 30-item self-administered questionnaire assessing upper-extremity functional limitations. Items are scored 1-5 and converted to a 0-100 scale, where higher scores indicate greater disability.

    6 weeks

  • Shoulder Range of Motion (ROM)

    Active shoulder flexion, abduction, external rotation, and internal rotation will be measured using a standard goniometer. Results will be recorded in degrees (°).

    6 weeks

Secondary Outcomes (6)

  • Shoulder Function (American Shoulder and Elbow Surgeons Score - ASES)

    6 weeks

  • Thoracic Kyphosis Angle (Spinal Mouse Assessment)

    6 weeks

  • Pain Catastrophizing (Pain Catastrophizing Scale - PCS)

    6 weeks

  • Anxiety and Depression (Hospital Anxiety and Depression Scale - HADS)

    6 weeks

  • Kinesiophobia (Tampa Scale of Kinesiophobia - TSK)

    6 weeks

  • +1 more secondary outcomes

Study Arms (2)

Conventional Rehabilitation Group

ACTIVE COMPARATOR

Participants undergoing reverse shoulder arthroplasty will receive a standard conventional rehabilitation program starting at postoperative 6 th week . The patient will receive treatment 5 days a week for 6 weeks, for a total of 30 sessions. The program consists of passive, active-assisted, and active/resisted exercises. Exercises Included: Passive / Assisted * Scapular mobilization * Scapular clock * Passive external rotation with a stick Passive → Active-Assisted * Active-assisted flexion and abduction with a stick * Glenohumeral joint mobilization Active / Light Resistance * Scapular retraction * Light-resistance strengthening of biceps, triceps, and serratus anterior using a theraband Active / Resistance * Theraband-based resisted biceps, triceps, and serratus anterior strengthening * Continuation of glenohumeral mobilization * Flexion and abduction above 90° * Posterior capsule stretching

Other: Conventional Rehabilitation Group

Depressor Muscle Strengthening Program

EXPERIMENTAL

Participants will receive specific strengthening exercises targeting the shoulder depressor muscles in addition to the conventional rehabilitation program. These exercises will be performed throughout the 6-week intervention period. Additional Exercises: Latissimus dorsi: Seated rowing exercise - 3 sets × 10 repetitions Pectoralis major: Supine fly exercise - 3 sets × 10 repetitions Teres major: Prone shoulder adduction, extension, and internal rotation exercise

Other: Conventional Rehabilitation GroupOther: Depressor Muscle Strengthening Group

Interventions

After randomization and baseline assessments, participants will undergo a standard 6-week postoperative shoulder rehabilitation program, consisting of range-of-motion exercises, scapular stabilization training, and progressive strengthening. No additional depressor muscle-specific exercises will be applied.

Conventional Rehabilitation GroupDepressor Muscle Strengthening Program

After randomization and baseline assessments, participants will receive a 6-week rehabilitation program consisting of conventional postoperative shoulder rehabilitation combined with a specific strengthening protocol targeting the shoulder depressor muscles.

Depressor Muscle Strengthening Program

Eligibility Criteria

Age65 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • Patients scheduled for primary reverse total shoulder arthroplasty Intact teres minor confirmed by physical examination (Hornblower's test) and intraoperative assessment Ability to participate in physiotherapy or a home exercise program

You may not qualify if:

  • Active infection Deltoid muscle insufficiency Inability or unwillingness to comply with randomization Prior shoulder arthroplasty on the same side Unwillingness to participate Inability to read or understand written instructions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Kırşehir Ahi Evran University

Kırşehir, 40100, Turkey (Türkiye)

RECRUITING

Central Study Contacts

Caner KARARTI, Assoc. Prof.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
Blinded assessor
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Randomized
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 15, 2025

First Posted

December 30, 2025

Study Start

January 2, 2026

Primary Completion (Estimated)

September 2, 2026

Study Completion (Estimated)

December 2, 2026

Last Updated

March 3, 2026

Record last verified: 2026-03

Locations