Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06631872

Implementing Surgery School Prehabilitation Using Telehealth

Led by University of Melbourne · Updated on 2025-08-27

515

Participants Needed

6

Research Sites

179 weeks

Total Duration

On this page

Sponsors

U

University of Melbourne

Lead Sponsor

P

Peter MacCallum Cancer Centre, Australia

Collaborating Sponsor

AI-Summary

What this Trial Is About

The physiological challenge of major surgery has been likened to running a marathon. In both cases, preparation is critical. Yet, many patients undergo major surgery without understanding the potential consequences. The STTARRS trial aims to test the effect of an education program delivered via telehealth in people preparing for lung or major abdominal cancer surgery , compared with usual care on the development of a respiratory complications after surgery. The secondary aims will be to determine the effect of the online education program for people preparing for lung or major abdominal cancer surgery compared to usual care on the following outcomes; acute hospital length of stay, surgical recovery, physical function and activity, self-efficacy, behaviour change, symptoms, health-related quality of life, number of days alive and out of hospital and health service usage and survival. This trial includes one sub-study. The sub-study will recruit eligible people preparing for lung cancer surgery. In the sub-study, 35 participants will receive an individualised inspiratory muscle training and walking program delivered and monitored by telehealth in addition to the main STTARRS trial intervention before surgery.

CONDITIONS

Official Title

Implementing Surgery School Prehabilitation Using Telehealth

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Preparing for lung cancer (open or video assisted) or major abdominal cancer surgery (e.g. upper GI, hepatobiliary or colorectal, open or video assisted)
  • Provide consent
  • Have primary treating surgeon approval
  • Proficient in English to understand testing, video interventions as well as outcome assessments
Not Eligible

You will not qualify if you...

  • Concurrent, actively treated other malignancy or history of other malignancy treated within the past year
  • Severe or unstable psychiatric, cognitive or substance abuse disorders, such that precludes informed consent or interferes with cooperation with trial requirements or current inpatients
  • Current inpatients or incarcerated
  • Surgery date booked <7 days from consent

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Trial Site Locations

Total: 6 locations

1

John Hunter Hospital

New Lambton Heights, New South Wales, Australia, 2305

Actively Recruiting

2

Princess Alexandra Hospital

Woolloongabba, Queensland, Australia, 4102

Actively Recruiting

3

Launceston General Hospital

Launceston, Tasmania, Australia, 7250

Not Yet Recruiting

4

Austin Health

Heidelberg, Victoria, Australia, 3084

Actively Recruiting

5

Royal Melbourne Hospital

Melbourne, Victoria, Australia, 3050

Actively Recruiting

6

Fiona Stanley Hospital

Perth, Western Australia, Australia, 6845

Actively Recruiting

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Research Team

L

Linda Denehy, B AppSc (Physio), PhD

CONTACT

J

Jamie Waterland, B Physio(Hons), PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

4

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