Investigating factors affecting outcomes after shoulder replacement surgery
Which Factors Influence the Outcome After Anatomical and Reverse Shoulder Arthroplasty? A Prospective Longitudinal Study With Randomized Group Allocation, Towards Better Rehabilitation Strategies
NA · Universiteit Antwerpen · NCT04258267
This study is trying to find out what factors before, during, and after shoulder replacement surgery can affect how well patients recover and feel afterward.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 97 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Universiteit Antwerpen (other) |
| Locations | 1 site (Deurne, Antwerp) |
| Trial ID | NCT04258267 on ClinicalTrials.gov |
What this trial studies
This study aims to explore various pre-, intra-, and post-operative factors that may influence the outcomes of shoulder arthroplasty, including pain, function, and quality of life. It will assess patient characteristics, surgical indications, and rehabilitation practices, comparing the effects of early versus delayed mobilization. Additionally, the study will evaluate the reliability of various assessment tests and the routines of orthopedic surgeons and physiotherapists involved in the procedure. By gathering comprehensive data, the study seeks to identify key factors that contribute to successful recovery after shoulder surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 and older who are scheduled for primary shoulder arthroplasty.
Not a fit: Patients undergoing revision shoulder surgery will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved recovery protocols and better outcomes for patients undergoing shoulder arthroplasty.
How similar studies have performed: Other studies have shown success in identifying factors influencing surgical outcomes, making this approach both relevant and potentially impactful.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult men and women \>= 18 years of age * Scheduled for primary shoulder arthroplasty Exclusion Criteria: * Revision surgery
Where this trial is running
Deurne, Antwerp
- AZ Monica — Deurne, Antwerp, Belgium (RECRUITING)
Study contacts
- Study coordinator: Anke Claes, PhD student
- Email: anke.claes@uantwerpen.be
- Phone: 0032498040863
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Arthroplasty, Replacement, Shoulder, "Influencing factors", Rehabilitation, "Anatomical shoulder arthroplasty", "Reverse shoulder arthroplasty"