RecruitingNot ApplicableNCT06631872

Implementing Surgery School Prehabilitation Using Telehealth

Implementing Tele-prehabilitation Education Into Cancer Care Pathways


Sponsor

University of Melbourne

Enrollment

515 participants

Start Date

Jan 22, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • 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.

Exclusion Criteria4

  • 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

Interventions

BEHAVIORALTele-prehabilitation education session: Surgery School

Online telehealth education program using videos and a live clinician facilitator

BEHAVIORALIndividualised Inspiratory Muscle Training and Walking Program

An individualised inspiratory muscle training and walking program delivered by a Physiotherapist using telehealth.

OTHERUsual Care

Usual care alone. Usual care will be reviewed every four months during the trial and site leads will be asked to provide information about any changes to usual hospital and medical care at their site.


Locations(6)

John Hunter Hospital

New Lambton Heights, New South Wales, Australia

Princess Alexandra Hospital

Woolloongabba, Queensland, Australia

Launceston General Hospital

Launceston, Tasmania, Australia

Austin Health

Heidelberg, Victoria, Australia

Royal Melbourne Hospital

Melbourne, Victoria, Australia

Fiona Stanley Hospital

Perth, Western Australia, Australia

View Full Details on ClinicalTrials.gov

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NCT06631872