Prehabilitation in Patients With Gynaecological Cancer Planned for Postponed Surgical Management: A Prospective Randomised Trial.

Status: Recruiting
Intervention Type: Other, Dietary supplement, Behavioral
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Prehabilitation refers to interventions aiming to improve patients' resilience and functional capacity before a known stressful event, e.g., scheduled surgery. These interventions usually consist of physical activity and psychological and nutritional support. There is substantial evidence of the positive effect of multimodal prehabilitation among patients treated surgically for non-gynaecological cancers; however, no prospective data are available in gynaecological cancer patients. PHOCUS trial is a prospective randomised trial aiming to evaluate the role of multimodal prehabilitation in patients with gynaecological cancer. Sixty-four patients will be randomised in single institution within 36 months with a 1:1 ratio into ARM A: control arm which will be provided with a basic information and standard of care support; ARM B: active arm undergoing multimodal prehabilitation composed of physical activity and psychological and nutritional support. All patients will be assessed at standard intervals (three times during the trial) by a spectrum of non-invasive tests, evaluating physical functional capacity, postoperative morbidity, nutritional status, level of stress and anxiety, and quality of life.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• Two groups of patients will be eligible for the trial:

• i) Epithelial ovarian cancer patients referred for NACT: a) FIGO stage III or IV disease; b) Patient is not a candidate for primary debulking surgery; c) Patient is a suitable candidate for standard of care combined chemotherapy; d) Patient is a candidate for interval.debulking surgery

• ii) Stage I or II endometrial cancer patients classifying as frail according to the validated modified Frailty Index: a) FIGO stage I or II; b) Patient is classified as frail; c) Patient is suitable candidate for hormonal therapy.

Contact Information
Primary
Jana Stribrna
jana.stribrna@vfn.cz
+420 224 967 432
Backup
Stefan Lednicky, MD.
stefan.lednicky@vfn.cz
Time Frame
Start Date: 2021-01-25
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 64
Treatments
No_intervention: A
Patients will be provided with a basic information and standard of care support.
Experimental: B
Active prehabilitation will be provided, composed of i) three physical activity-related interventions provided by a physical and rehabilitation medicine (PRM) specialist; iii) three 30 min consultations regarding nutritional status with physician or nutrition specialist; ii) three sessions with psychologist.
Sponsors
Leads: Charles University, Czech Republic
Collaborators: University Hospital Ostrava, University Hospital Pilsen, University Hospital Olomouc, The Faculty Hospital Na Bulovce

This content was sourced from clinicaltrials.gov