PRIORITY-CONNECT 2 Pilot Trial

Last updated: April 23, 2024
Sponsor: Surgical Outcomes Research Centre (SOuRCe)
Overall Status: Active - Recruiting

Phase

N/A

Condition

Esophageal Cancer

Pancreatic Cancer

Gastric Cancer

Treatment

Preoperative Nutrition

Postoperative Exercise

Preoperative Psychology

Clinical Study ID

NCT06212700
X23-0399
  • Ages > 18
  • All Genders

Study Summary

The provision of preoperative interventions (prehabilitation: including exercise, nutrition, and psychological treatment) have been reported to reduce postoperative complications by as much as 50% and reduce hospital stay by up to 4 days compared to standard of care. Postoperative multimodal interventions are likely to further benefit patients facing new challenges (e.g. stoma care), and reduce post discharge complications.

Therefore the Virtual Multimodal hub of PRIORITY-CONNECT 2 Pilot Trial aims to primarily; determine the feasibility of incorporating a virtual multimodal program into the preoperative and postoperative period for patients undergoing gastrointestinal cancer surgery, the acceptability to patients, clinicians and carers of the virtual multimodal program and the acceptability to patients of being randomised to the virtual multimodal program or usual care.

The secondary aim is to obtain pilot data on the likely difference in key outcomes (30 days postoperative complications, quality of life, days at home and alive at 30 days - DAH30, implementation outcomes and cost outcomes) to inform the development of a substantive randomised clinical trial.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adults aged ≥18 years undergoing major gastrointestinal elective surgery, includingliver, pancreas, oesophagus, gastric and colorectal cancer resections with curativeintent
  • Consulting with a gastrointestinal cancer surgeon at least 1 week prior to scheduledsurgery

Exclusion

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 computerwith camera) or no internet connection

Study Design

Total Participants: 20
Treatment Group(s): 11
Primary Treatment: Preoperative Nutrition
Phase:
Study Start date:
February 12, 2024
Estimated Completion Date:
December 22, 2025

Connect with a study center

  • Chris O'Brien Lifehouse

    Sydney, New South Wales 2050
    Australia

    Active - Recruiting

  • Royal Prince Alfred Hospital, Surgical Outcomes Research Centre (SOuRCe)

    Sydney, New South Wales 2050
    Australia

    Active - Recruiting

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