Exercise- and education-based prehabilitation before total knee arthroplasty: a pilot study.
Pascale Gränicher, Loes Mulder, Ton Lenssen...
https://pubmed.ncbi.nlm.nih.gov/38192160Actively Recruiting
Led by University of Jaén · Updated on 2026-02-13
44
Participants Needed
1
Research Sites
8 weeks
Total Duration
U
University of Jaén
Lead Sponsor
H
Hospital Clinico Universitario San Cecilio
Collaborating Sponsor
Researchers are studying the effects of a prehabilitation program on patients with hip or knee osteoarthritis who are awaiting arthroplasty surgery. Osteoarthritis is a joint disease causing pain, stiffness, and reduced function, often affecting the hip and knee. This study aims to find out whether prehabilitation can improve recovery times, functional ability, and psychological wellbeing after surgery, offering a non-drug, non-invasive treatment option. Participants in the intervention group will follow a 6-week supervised prehabilitation program before surgery, including strength, balance, cardiovascular, and flexibility exercises. After surgery, they will receive the same rehabilitation program as the control group. The control group will begin a post-operative physiotherapy and home exercise program after hospital discharge. The study compares these approaches to see how prehabilitation affects outcomes. During the study, participants will be assessed on quality of life, lower limb function, strength, pain, psychological factors, sleep quality, and medication use at various points from before prehabilitation through 24 weeks after surgery. Researchers will monitor adherence to therapy and measure body composition and biochemical markers. The goal is to understand how prehabilitation influences recovery and overall health in patients undergoing hip or knee replacement.
CONDITIONS
Effectiveness of a Prehabilitation Program for Hip or Knee Arthroplasty Surgery.
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You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 weeks
Participants in the intervention group undergo a 6-week prehabilitation program supervised by a physiotherapist, including 3 sessions per week lasting 30 to 45 minutes each, plus daily home exercises focusing on flexibility and proprioception.
3 supervised sessions per week and daily home exercises
Duration - 1 to 2 days post-surgery
Participants undergo hip or knee arthroplasty surgery followed by immediate post-operative care.
1 hospital stay for surgery and immediate recovery
Duration - Up to 18 weeks following surgery
Participants in both groups follow a post-operative physiotherapy program along with a home exercise program demonstrated before hospital discharge.
Multiple physiotherapy sessions and home exercises as prescribed
Duration - Up to 24 weeks from study start
Participants complete follow-up assessments evaluating quality of life, functionality, strength, pain, psychological aspects, sleep quality, analgesic use, therapeutic adherence, and other clinical parameters up to 24 weeks after starting the study.
Visits at week 6, week 9, and week 24 for assessments
Total: 1 location
1
Hospital Universitario San Cecilio- Distrito Sanitario Metropolitano Granada
Granada, Spain, 18012
Actively Recruiting
I
IRENE MARIA IMLP LOPERA, Investigator
I
IRENE IMAGINO LOPERA, Principal Investigator
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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