Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07275164

High-Intensity Interval Training (HIIT) for Chronic Inflammatory-Driven Shoulder Pain: A Feasibility Study

Led by Universiteit Antwerpen · Updated on 2026-02-13

30

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying whether high-intensity interval training (HIIT) is feasible and acceptable for people with long-lasting shoulder pain, such as rotator cuff-related pain or frozen shoulder. Many patients do not fully recover with current treatments, and inflammation, metabolic changes, and nervous system imbalances may contribute to ongoing pain. This feasibility study involves 30 participants, including 15 with persistent shoulder pain and 15 without symptoms, to explore these systemic factors and the practicality of using HIIT. Participants with shoulder pain will complete two sessions: one to measure maximum exercise capacity on a cycle ergometer and another combining assessments with a personalized 20-minute HIIT session. The HIIT consists of five one-minute high-intensity cycling intervals at maximum capacity, each followed by one minute of active rest. Controls will undergo a single assessment session without exercise. The study will measure inflammation, metabolic markers, autonomic and sensory nervous system functions, and participant responses to the HIIT session. Throughout the study, participants will have clinical assessments including blood tests, blood pressure, body composition measurements, pain sensitivity tests, and questionnaires about symptoms and quality of life. Researchers will monitor adherence, motivation, safety, and acceptability of HIIT, as well as any side effects up to three days after exercise. The study aims to inform larger future trials and explore systemic approaches to managing chronic shoulder pain. Participation will last through the assessment and HIIT sessions, with no extended follow-up period.

CONDITIONS

Brief Title

HIIT for Inflammatory-driven Shoulder Pain.

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Shoulder pain longer than 3 months
  • Diagnosis of rotator cuff related shoulder pain or frozen shoulder
  • Understanding Dutch in speaking and writing
  • Adults aged 18 years or older
  • Control group participants must understand Dutch in speaking and writing
Not Eligible

You will not qualify if you...

  • Under 18 years old
  • Shoulder surgery or trauma within the past year
  • Neurological, cancer, or neuromuscular diseases
  • Osteoarthritis, cervical or acromioclavicular joint pathology
  • Heavy physical exertion within 48 hours before testing
  • 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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Assessment

Duration - 1 day

Participants undergo baseline assessments including shoulder pain and disability, pain intensity, quality of life, inflammation markers, metabolic markers, autonomic and somatosensory functions.

1 visit (in-person)

Treatment

Duration - Approximately 1 day

Participants with shoulder pain complete a supervised high-intensity interval training (HIIT) session on a cycle ergometer consisting of five 1-minute intervals at VO₂max with active rest periods.

1 visit (in-person)

Follow-up

Duration - Up to 3 days

Participants are monitored for adverse events and safety for up to 3 days after the training and assessment session.

No visits required

Trial Site Locations

Total: 1 location

1

Universiteit Antwerpen

Wilrijk, Belgium, 2610

Actively Recruiting

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Research Team

M

Michel Mertens, PhD

M

Mira Meeus, PhD

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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