Pioneering Pre- and Post-Operative Integrative Care to Improve Thoracic Cancer Quality of Care - The Thoracic Peri-Operative Integrative Surgical Care Evaluation (POISE) Trial - Stage III

Who is this study for? Patients with thoracic cancer
What treatments are being studied? Vitamin D3+Coriolus Versicolor+Trident SAP 66:33 Lemon+Probiotic Pro12+Provitalix Pure Whey Protein+Theracurmin 2X+Green Tea Extract+Nutrition Recommendations+Physical Activity Recommendations+Psychological Recommendations
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Dietary supplement, Other, Behavioral
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Despite enormous advances in thoracic surgery and oncology, two critical issues concern patients undergoing curative-intent surgery for lung, gastric and esophageal cancer: first, a majority (\ 60%) of patients experience minor and major adverse events occurring during and in the days following surgery; second, patients worry about the significant risk of cancer recurrence and mortality months to years after surgery. These issues, combined with side effects of chemotherapy and radiation, have detrimental effects on health-related quality of life (HRQoL). On a deeper level, there is the problem of an ongoing failure to integrate and evaluate the best of what complementary medicine has to offer surgical oncology care. Too many clinical trials focus on single agent therapies, rather than broad multi-faceted individualized and integrative care interventions that are used in real world settings. The Thoracic POISE project has the overarching goal of improving care for thoracic cancer patients by impacting HRQoL, reducing surgical adverse events, prolonging overall survival and pioneering integrative care delivery.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• • Adults eligible for complete resection of lung, gastric or esophageal cancer

Locations
Other Locations
Canada
The Ottawa Hospital
RECRUITING
Ottawa
Michael Garron Hospital
RECRUITING
Toronto
Contact Information
Primary
Anna Fazekas, MA, CCRP
afazekas@toh.ca
613-737-8899
Backup
Mark Legacy, BSc
mlegacy@thechi.ca
613-792-1222
Time Frame
Start Date: 2022-04-04
Estimated Completion Date: 2029-12-01
Participants
Target number of participants: 20
Treatments
Experimental: Integrative Care (Treatment)
Participants in the Integrative arm will receive standard surgical and oncologic care at The Ottawa Hospital plus complementary care guided by a naturopathic doctor at The Centre for Health Innovation
No_intervention: Standard Care (Control)
Participants in the control arm will receive standard surgical and oncologic care at The Ottawa Hospital
Sponsors
Collaborators: University of Ottawa, The Centre for Health Innovation, The Canadian College of Naturopathic Medicine, Lotte & John Hecht Memorial Foundation
Leads: Ottawa Hospital Research Institute

This content was sourced from clinicaltrials.gov