Efficacy of Pre-Operative Prehabilitation in Patients Undergoing Open Surgery for Abdominal Aortic Aneurysm
Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
This is a pilot, prospective, randomized control trial that aim to provide a first estimation of the 3-month post-operative variation in the functional recovery of patients who benefited from an outpatient pre-habilitation program and patients who did not benefit from it.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:
• Patient with an abdominal aortic aneurysm (Thoraco-abdominal aneurysm type 4/Supra renal/Juxta-renal/Sub renal) treated with conventional surgery.
• Surgical indication of aneurysm by size (50-55mm)
Locations
Other Locations
France
Uh Toulouse
RECRUITING
Toulouse
Contact Information
Primary
Aurélien Hostalrich, MD
hostalrich.a@chu-toulouse.fr
05 61 32 26 20
Backup
Virgile Pinelli, MD
pinelli.v@chu-toulouse.fr
05 61 32 26 20
Time Frame
Start Date: 2022-12-06
Estimated Completion Date: 2025-06
Participants
Target number of participants: 60
Treatments
Experimental: PREHABILITATION GROUP
Initial visit with the adaptive rehabilitation physician, 6-8 weeks prior to surgery:~* Clinical examination with Wood classification description of impairments, activity limits and participation restrictions.~* Assessment of environmental resources~* Definition with the patient of the extended ambulatory pre-habilitation protocol, identification with the post-operative rehabilitation pathway,~* Provide the patient with a follow-up workbook of the personalized pre-approval protocol and, if the patient's condition requires it, orders for physiotherapy.~Then apply the ambulatory pre-approval protocol defined with the adaptive rehabilitation physician.~\- Post-operative follow-up visits with the surgeon (gathering the necessary information for comparative follow-up).~Mail-out of WHODAS 2.0 EQ-5D-5L and DIJON questionnaires at 3 and 6 months post-operative.
No_intervention: CONTROL GROUP
Support without pre-approval with application of other common practices of the service.~Post-operative follow-up visits with the surgeon (gathering the necessary information for comparative follow-up).~Mail-out of WHODAS 2.0 EQ-5D-5L and DIJON questionnaires at 3 and 6 months post-operative.
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Toulouse