Ireland
--:--IST
Recruiting Not applicable

Strengthening Exercises for Humeral Head Depressor Muscles

NCT07309796 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-02
Last updated
2026-03-03

Condition(s) studied

Reverse Shoulder ArthroplastyDepressor Muscle TrainingShoulder Rehabilitation

Investigational drug(s) / intervention(s)

Conventional Rehabilitation GroupDepressor Muscle Strengthening Group

Conventional Rehabilitation Group: 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.

Depressor Muscle Strengthening Group: 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.

Study 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.

Eligibility

Sex
ALL
Min age
65 Years
Max age
90 Years
Healthy volunteers
No
Inclusion Criteria: * 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 Exclusion Criteria: * 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

Primary outcome measure(s)

  • Pain Intensity (Visual Analog Scale - VAS) — 6 weeks
    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.
  • Upper Extremity Disability (Disabilities of the Arm, Shoulder and Hand Questionnaire - DASH) — 6 weeks
    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.
  • Shoulder Range of Motion (ROM) — 6 weeks
    Active shoulder flexion, abduction, external rotation, and internal rotation will be measured using a standard goniometer. Results will be recorded in degrees (°).

Trial sites (1)

FacilityCityRegionStatus
Kırşehir Ahi Evran University Kırşehir Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07309796 on ClinicalTrials.gov ↗ ← All trials in Turkey