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Multimodal Geriatric Pre-authorization Before Scheduled Orthopedic Surgery — PRE4OS  

Osteoarthritis Clinical Trial

Official title:
Multimodal Geriatric Pre-authorization Before Scheduled Orthopedic Surgery

Clinical Trial Summary

The main objective of this multicentric, prospective and interventional study is to assess the feasibility of multimodal prehabilitation in patients aged 75 years or older with surgical indication for coxarthrosis or severe gonarthrosis

Clinical Trial Description

This study consists of a pre-established surgical preparation program in cooperation with physiotherapists or physical activity instructors, dieticians, psychologists, physical therapists and nurses. This innovative program improves muscle strength, balance and walking of the study patients. It also allows for faster and better recovery of their physical fitness and intellectual abilities after surgery. These interventions will be performed in day admission (DA) and at home and will consist of training, a diet program to strengthen the muscles and balance of the patients participating in the study. Patients who agree to participate in the study will receive interventions for 6 weeks prior to surgery, partly in a day hospital and partly at home, including: - Muscle rehabilitation developed with a physiotherapist or physical activity instructor - Nutritional support (dietician at 1st, 3rd, and 6th day admission (DA), referring geriatrician) - Cognitive and physical stimulation "Exergame" (Genious Healthcare); with only cognitive exercises at home - Psychological support by a psychologist - Information in the form of videos on the main risks and important points to know and prepare before and after surgery - 1 follow-up call per week made by the PRE4OS referent between each day admission (DA) to assess patient satisfaction, any limitations encountered, possible exercises at home, the occurrence of possible adverse effects - 1 hour per week home adapted physical activity session by the Siel Bleu association ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05062109
Study type Interventional
Source Gérond'if
Contact Isabelle Dufour
Phone +33 (0)185781010
Email isabelle.dufour@gerondif.org
Status Recruiting
Phase N/A
Start date June 16, 2021
Completion date December 2023
View Details
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