Actively Recruiting
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
Eligibility Criteria
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
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
AI-Screening
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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
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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