Virtual multimodal program for patients undergoing gastrointestinal cancer surgery
Virtual Multimodal Hub for Patients Undergoing Major Gastrointestinal Cancer Surgery - PRIORITY-CONNECT 2 Pilot Randomised Type I Hybrid Effectiveness-Implementation Trial
This study is testing a new online program that offers exercise, nutrition, and mental health support for patients having major gastrointestinal cancer surgeries to see if it helps them recover better than standard care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Surgical Outcomes Research Centre (SOuRCe) Research network |
| Locations | 2 sites (Sydney, New South Wales and 1 other locations) |
| Trial ID | NCT06212700 on ClinicalTrials.gov |
What this trial studies
This trial evaluates the feasibility and acceptability of a virtual multimodal program that includes preoperative and postoperative interventions such as exercise, nutrition, and psychological support for patients undergoing major gastrointestinal cancer surgeries. The program aims to reduce postoperative complications and hospital stays compared to standard care. Participants will be randomized to either the virtual program or usual care to assess outcomes and patient satisfaction. The study focuses on patients with liver, pancreas, oesophageal, gastric, and colorectal cancers.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who are scheduled for major elective gastrointestinal surgery with curative intent.
Not a fit: Patients with cognitive impairments that prevent informed consent or those without access to smart devices or internet may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly reduce postoperative complications and improve recovery times for patients undergoing gastrointestinal cancer surgery.
How similar studies have performed: Other studies have shown promising results with prehabilitation approaches, suggesting potential success for this virtual multimodal program.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged ≥18 years undergoing major gastrointestinal elective surgery, including liver, pancreas, oesophagus, gastric and colorectal cancer resections with curative intent * Consulting with a gastrointestinal cancer surgeon at least 1 week prior to scheduled surgery Exclusion Criteria: * Cognitive impairment such that they are unable to provide informed consent * No access to a smart device (including mobile phone, tablet, laptop or desk computer with camera) or no internet connection
Where this trial is running
Sydney, New South Wales and 1 other locations
- Chris O'Brien Lifehouse — Sydney, New South Wales, Australia (Recruiting)
- Royal Prince Alfred Hospital, Surgical Outcomes Research Centre (SOuRCe) — Sydney, New South Wales, Australia (Recruiting)
Study contacts
- Study coordinator: Daniel Steffens, PhD
- Email: Daniel.Steffens@health.nsw.gov.au
- Phone: +61 02 9515 3203
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.