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Clinical Trials/NCT05375292
NCT05375292RecruitingNot Applicable

Efficacy of Pre-Operative Prehabilitation in Patients Undergoing Open Surgery for Abdominal Aortic Aneurysm

University Hospital, Toulouse1 site in 1 country60 target enrollmentStarted: December 6, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
60
Locations
1
Primary Endpoint
functional WHODAS 2.0 score

Study Overview

Brief 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.

Detailed Description

Open surgery of abdominal aortic aneurysms (AAA) is the reference treatment in a large number of cases. This is a heavy procedure performed in patients around 70 years of age.

In post-operative open aortic surgery, a stay in aftercare and rehabilitation is often necessary, especially in fragile patients.

The goal is to increase the patient's overall functional status to allow him to move away from the threshold below which he loses his independence for activities of daily living.

The pre-habilitation protocol includes 3 parts :

  1. Oral nutrition ensures adequate caloric and protein intake to support muscle anabolism
  2. Muscle building over a few sessions with a liberal physiotherapist to learn exercises and then independently
  3. Cardio-respiratory endurance.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •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)

Exclusion Criteria

  • •- Patient requiring urgent management that does not allow for a pre-authorisation protocol of at least 6 weeks.

Arms & Interventions

PREHABILITATION GROUP

Experimental

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.

Intervention: PREHABILITATION (Other)

CONTROL GROUP

No Intervention

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.

Outcomes

Primary Outcomes

functional WHODAS 2.0 score

Time Frame: 3 months after the open surgery for AAA

the WHODAS 2.0 score ranges from 12 to 60 : 12 representing no difficulty at all, 60 representing worst difficulty to engage in usual activities

functional WHODAS 2.0 score

Time Frame: T0 : Right after the open surgery for AAA

the WHODAS 2.0 score ranges from 12 to 60 : 12 representing no difficulty at all, 60 representing worst difficulty to engage in usual activities

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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