Feasibility of high-dose multimodal prehabilitation for women awaiting gynecologic cancer surgery
Official title: Assessing Delivery Approaches for Prehabilitation Trials in Gynecologic Cancer: A Pilot Feasibility Patient-Preference Trial
Run by Queen's University · NCT07609082 · Data updated 2026-11-12
This study tests whether a high-dose, multimodal prehabilitation program can be delivered before gynecologic cancer surgery and whether patients prefer in-person, remote, or education-only approaches.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 36 (estimated) |
| Sponsor | Queen's University Academic / other |
| Drugs / interventions | chemotherapy |
| Locations | 1 site (Kingston, Ontario) |
| Status | Recruiting |
| Started | May 14, 2027 |
| Main results expected | May 14, 2027 |
| Study ends | May 14, 2027 |
| Registry record updated | October 30, 2026 |
| Trial ID | NCT07609082 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women aged 18 or older scheduled for cytoreductive surgery for a gynecologic mass suspicious or confirmed of cancer, with at least 3 weeks before surgery and able to consent and understand English.
✕Probably not a fit
Patients who are unable to participate in an exercise program due to health or logistical barriers may not experience direct benefits.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
ADAPT is a single-center pilot trial comparing three prehabilitation delivery models—in-person, remote with coaching and a web app, and education-only—for women preparing for ovarian cancer surgery. The study aims to see if participants can reach at least 10 MET-hours per week of aerobic exercise before surgery and which delivery method patients prefer. It evaluates feasibility, acceptability, and practicality to inform future larger trials, with attention to barriers such as travel and scheduling. The trial also considers how multimodal prehabilitation may influence postoperative recovery by targeting fitness, nutrition, and psychological support. Participants may choose their group or be randomly assigned, and the study is designed to identify the most workable approach for gynecologic cancer patients undergoing cytoreductive surgery.
Why it matters
Potential benefit: If successful, the program could improve patients' fitness and recovery after surgery and guide future care models for gynecologic cancer patients.
How similar studies have gone: Prior studies suggest prehabilitation may improve recovery, but results vary; this trial explores delivery feasibility to optimize future evidence.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female * Aged ≥18 years * Scheduled for cytoreductive surgery for a gynecologic mass suspected or confirmed of cancer * Surgery planned ≥3 weeks from time of booking * No contraindications to exercise on the CSEP Get Active Questionnaire * Able to provide written informed consent * Able to understand and communicate in English Exclusion Criteria: * Pregnancy * Cervical pathologies * Surgery scheduled \<3 weeks from booking * Receiving neoadjuvant chemotherapy * Positive contraindications to exercise on the CSEP Get Active Questionnaire * End-stage or advanced renal disease limiting safe protein supplementation * Malnutrition as assessed by a registered dietician
Where it's running
-
Kingston Health Sciences Centre
Kingston, Ontario, Canada Recruiting
Study contacts
- Principal investigator: Jordan Leitch, MSc, MD, FRCPC — Queen's University
- Study coordinator: Deborah DuMerton
- Email: deborah.dumerton@kingstonhsc.ca
- Phone: 613-484-7322
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Pre-surgery conditioning and optimization for hip or knee replacement
This will try a tailored pre-surgery program for adults with higher surgical risk (ASA ≥3) who are waiting at least eight weeks for elective hip or knee replacement to see if it improves recovery and reduces complications.
-
Immunonutrition and Brain Monitoring to See if Delirium Happens After Gynecologic Cancer Surgery
This study tests whether a preoperative immunonutrition scoring plus intraoperative brain monitoring can help predict or relate to postoperative delirium in women aged 65 and older undergoing major gynecologic cancer surgery.
-
Preoperative functional optimization for adults undergoing major cardiac or abdominal surgery
This study tests a four‑week prehabilitation program to improve fitness before elective major cardiac or abdominal surgery.
-
Multimodal Prehabilitation for Gastric Cancer Patients
This program tests whether a combined pre- and post-operative wellness plan can reduce inflammation after gastric cancer surgery in adults.
-
Wireless home prehabilitation for older adults with NSCLC awaiting lung surgery
This study tests whether a personalized home exercise program guided by wearable devices can improve lung function for older NSCLC patients preparing for curative lung surgery.
-
Prophylactic subcutaneous drainage after gynecologic cancer surgery
This study tests whether placing a small drain under the skin after gynecologic cancer surgery helps prevent wound problems in women with thicker tissue under the skin.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.