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Clinical Trials in Turkey / NCT07784543
Starting soon Not applicable

Effects of Aerobic Exercise on Shoulder Pain, Disability, and Ultrasonographic Outcomes in Patients With Type 2 Diabetes Mellitus With Supraspinatus Tendinopathy

NCT07784543 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-25
Last updated
2026-08-27

Condition(s) studied

Supraspinatus TendinopathyType 2 Diabetes Mellitus (T2DM)

Investigational drug(s) / intervention(s)

Conventional Shoulder RehabilitationAerobic Exercise

Conventional Shoulder Rehabilitation: Conventional physical therapy will be administered 5 days per week for 6 weeks (30 sessions). The program will include heat therapy, TENS, therapeutic ultrasound, and supervised shoulder-specific exercises, including range-of-motion, stretching, scapular stabilization, and rotator cuff strengthening exercises.

Aerobic Exercise: In addition to conventional shoulder rehabilitation, participants will perform moderate-intensity treadmill aerobic exercise (50-60% of heart rate reserve) 5 days per week for 6 weeks. Sessions will initially last 30 minutes (5-minute warm-up, 20-minute exercise, and 5-minute cool-down) and will increase to 40 minutes after Week 4. All sessions will be supervised by a physiotherapist and conducted according to appropriate safety protocols.

Study summary

Type 2 diabetes mellitus (T2DM) is a chronic disease characterized by elevated blood glucose levels over a prolonged period. If left untreated, it can lead to serious and long-term vascular and neurological complications. It is also a major cause of morbidity due to specific microvascular complications (retinopathy, nephropathy, and neuropathy), macrovascular complications (ischemic heart disease, stroke, and peripheral vascular disease), and reduced quality of life.

There are studies in the literature investigating conventional and shoulder-specific treatments for various shoulder pathologies in patients with type 2 diabetes mellitus (T2DM) . However, very few studies have investigated the effectiveness of aerobic exercise. The investigators identified only one study that evaluated the effects of aerobic exercise on pain and range of motion in patients with T2DM and adhesive capsulitis.

In the present study, the investigators aim to demonstrate that aerobic exercise results in statistically significant improvements in shoulder pain, functional disability, and the structural characteristics of the supraspinatus tendon, as assessed by ultrasonography and elastography, in participants with T2DM and supraspinatus tendinopathy. The investigators believe that the findings of this study will provide scientific evidence to support the development of more effective and comprehensive rehabilitation protocols for participants with diabetes and shoulder pain.

Eligibility

Sex
ALL
Min age
30 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Aged 30-70 years. * Having a diagnosis of type 2 diabetes mellitus (T2DM) for more than 1 year. * Having unilateral or bilateral shoulder pain for at least 3 months and a diagnosis of supraspinatus tendinopathy confirmed by magnetic resonance imaging (MRI). * Having a pain intensity score of ≥3 on the Visual Analog Scale (VAS). * No participation in regular exercise during the past 6 months Exclusion Criteria: * Having received shoulder rehabilitation within the past 6 months. * Having a full-thickness tear of the supraspinatus tendon. * Having a history of fracture, surgery, or injection in the upper extremity within the past 6 months. * Having a diagnosis of a neuromuscular disease, rheumatic disease, or severe cardiovascular disease. * Having advanced diabetic complications. * Having any condition that contraindicates or prevents participation in aerobic exercise.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Pamukkale University, Denizli Denizli Turkey (Türkiye)

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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 NCT07784543 on ClinicalTrials.gov ↗ ← All trials in Turkey