Language: BG BG
← Back to results
Recruiting Not applicable NCT06631872

Implementing Surgery School Prehabilitation Using Telehealth

No applicable phase (e.g. observational)
Conditions: Adults Waiting to Undergo Lung Cancer or Major Abdominal, Open or Video Assisted Cancer Surgery

Sponsor: University of Melbourne

trial.available_in: БГ
Overview
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.
Who can participate
Inclusion Criteria: * 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 Criteria: * 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
Locations 1
Australia (1)
John Hunter Hospital
New Lambton Heights , New South Wales
Technical details
Status
Recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
22.01.2025
Completion date
01.07.2028
Registry ID
NCT06631872
Source
anzctr
trial.inquiry_btn

Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.