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Clinical Trials in Austria / NCT05355909
Recruiting Not applicable

High Intensity PreHab Before Major Abdominal Surgery

NCT05355909 · tracked via the Priya Life Science Austria tracker
Phase
Not applicable
Started
2022-08-01
Last updated
2025-03-26

Condition(s) studied

Prehabilitation

Investigational drug(s) / intervention(s)

Individualized high intensity preoperative fitness training

Individualized high intensity preoperative fitness training: The individualised training program consists of stamina training, interval training and strength training. The personalised fitness training will be designed based on the FITT-VP (frequency, intensity, time, type, volume, progression) of the American College of Sports Medicine (ACSM) and will contain 6 training session within 2 weeks under supervision of professional sport physicians.

Study summary

The risk for major cardiac cardiovascular events (MACE) within the first 30 day after surgery is nit only associated to the patient relate risk factors but also to the kind of surgery. Surgical interventions can be distinguished infield risk (MACE \<1%), moderate risk (MACE 1-5%) and high risk (MACE \> 5%). In addition with patient related risk factors it can raise to values of 40%.

The preoperative aerobic fitness \[oxygen uptake (VO2) at the ventilatory anaerobic threshold (VAT) \<11 mL/kg/min\] has been shown of particularly interest in identifying patients at increased risk of postoperative complications. In the last decade major interest was put in the question whether a preoperative personalised physical training may have beneficial effect on the preoperative fitness and on the occurrence of postoperative complications. In some small studies this benefit has been shown for abdominal and thoracic surgery.

However some of those studies are controversially discussed because of missing randomisation and methodical issues. Also most of the studies needs a four week training period. This may lead to ethical and logostical problems oncologic patients.

The aim of this study is to assess the effect of a personalised, high intensity trains program of two weeks on the preoperative fitness.

Eligibility

Sex
ALL
Min age
18 Years
Max age
99 Years
Healthy volunteers
No
Inclusion Criteria: * ASA I-III * BMI 18 - 35kg/m2 * Signed informed consent * Elective abdominal surgery with moderate to high risk Exclusion Criteria: * Pregnancy of lactation * Major trauma or massive haemorrhage with the last two weeks * Inclusion of the patient in a interventional study * Contraindication for preoperative fitness training or ergometry * Transplantation surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Medical University Hospital Innsbruck Tyrol Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05355909 on ClinicalTrials.gov ↗ ← All trials in Austria