Actively Recruiting
Multimodal Biopsychosocial Teleprehabilitation for Total Knee Arthroplasty
Led by Universitair Ziekenhuis Brussel · Updated on 2024-08-22
60
Participants Needed
2
Research Sites
108 weeks
Total Duration
On this page
Sponsors
U
Universitair Ziekenhuis Brussel
Lead Sponsor
V
Vrije Universiteit Brussel
Collaborating Sponsor
AI-Summary
What this Trial Is About
Knee replacement surgeries are one of the most frequently performed elective surgeries, with approximately 29,000 such procedures carried out annually in Belgium. Although these surgeries have been increasingly refined over the years, leading to better surgical outcomes, there is still room for improvement in terms of pre-surgical biopsychosocial patient preparation. Such preparation aims to optimally inform patients before their surgery and to start preparing them for rehabilitation and resumption of activities after surgery. Therefore, we aim to assess the added value and feasibility of prehabilitation within the knee replacement care pathway. The primary objective is to investigate the feasibility, acceptability and safety of multimodal biopsychosocial teleprehabilitation (BPS-teleprehab) for people undergoing total knee arthroplasty (TKA). The secondary objective is to explore the effect of BPS-teleprehab versus best-evidence preoperative advice for people undergoing TKA on activity outcomes, functioning, pain, symptoms of central sensitization, quality of life, cognitive-emotional factors, joint awareness, satisfaction with the surgery, healthcare and medication use and productivity loss. The tertiary objective is to explore baseline associations between the collected outcome measures, demographics and medical data in people scheduled for TKA. Furthermore, this pilot trial will inform potential protocol modifications in prepara- tion of an eventual fully powered randomized controlled trial to investigate the ef- fectiveness of BPS-teleprehab in people undergoing TKA.
CONDITIONS
Official Title
Multimodal Biopsychosocial Teleprehabilitation for Total Knee Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- People scheduled for elective primary total knee arthroplasty at one of the participating hospitals
- Age over 18 years
- Able to speak and read Dutch
You will not qualify if you...
- Performing activities causing breathlessness for 300 minutes or more per week on average
- Having orthopedic, neurological, cardiovascular, or other conditions that contraindicate moderate physical activity
- Cognitive impairment (score of 11 or higher on 6-item Cognitive Impairment Test or unable to understand study instructions)
- Having uncontrolled inflammatory arthritis such as rheumatoid arthritis or gout
- Having uncontrolled psychiatric disorders
- Active cancer or undergoing active cancer treatment (except hormonal maintenance therapy)
- Undergoing emergency (non-elective) total knee arthroplasty
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Ziekenhuis Geel
Geel, Antwerpen, Belgium, 2440
Not Yet Recruiting
2
Universitair Ziekenhuis Brussel
Brussels, Brussels Capital, Belgium, 1090
Actively Recruiting
Research Team
E
Eva Huysmans, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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