Actively Recruiting
HIIT for Inflammatory-driven Shoulder Pain.
Led by Universiteit Antwerpen · Updated on 2026-02-13
30
Participants Needed
1
Research Sites
42 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This feasibility study investigates whether high-intensity interval training (HIIT) is feasible and acceptable for individuals with long-term shoulder pain where low-grade inflammation is suspected. Many patients do not recover fully with current local treatments, and systemic factors such as inflammation, and metabolic changes, additionally disturbances in the functioning of the nervous system often seem to play a role. HIIT is a time-efficient form of exercise that has been shown to improve inflammation and metabolic values and positively influence the balance of the nervous system. In this feasibility study, the investigators are enrolling 15 individuals with persistent shoulder pain (diagnosed with rotator cuff-related shoulder pain or frozen shoulder) with \>3 months of symptoms, and 15 individuals without shoulder complaints. All participants will undergo measurements of inflammatory levels, glycosylated hemoglobin (HbA1c), blood pressure, body composition, pain sensitivity tests, and complete questionnaires about autonomic complaints and quality of life. Participants with shoulder pain will also perform one personalized HIIT session on a cycle ergometer. The investigators will assess whether participants accept a systemic intervention for their shoulder pain, if they are cooperative, and how they feel about the session; additionally, any side effects will be recorded. The aim is to determine whether HIIT is practically feasible and safe for this group and whether there are indications that systemic factors such as inflammation and nervous system function are associated with persistent shoulder pain. The outcome will determine whether follow-up research with a larger study is worthwhile.
CONDITIONS
Official Title
HIIT for Inflammatory-driven Shoulder Pain.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Shoulder pain lasting more than 3 months
- Diagnosis of rotator cuff related shoulder pain or frozen shoulder
- Understanding Dutch in speaking and writing (shoulder pain group)
- Understanding Dutch in speaking and writing (control group)
You will not qualify if you...
- Under 18 years old
- Shoulder surgery or trauma in the past year (shoulder pain group)
- Neurological, cancer, or neuromuscular disease (shoulder pain group)
- Osteoarthritis, cervical or AC joint pathology (shoulder pain group)
- Heavy physical exertion within 48 hours before testing (shoulder pain group)
- Recent or recurrent neck/shoulder pain (control group)
- Systemic or neurological disease (control group)
- Psychiatric disorders (control group)
- Pregnancy or breastfeeding (control group)
- Use of pain medication within 48 hours before testing (control group)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Universiteit Antwerpen
Wilrijk, Belgium, 2610
Actively Recruiting
Research Team
M
Michel Mertens, PhD
CONTACT
M
Mira Meeus, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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