Multidimensional Burden of Platinum Resistant Ovarian Cancer (PROC) on Patients and Caregivers in Canada
1 other identifier
observational
150
1 country
1
Brief Summary
Filling the gap in Canadian evidence on the burden of PROC on QoL is essential. It will help better understand the impact of PROC on multiple aspects of the lives of patients and their caregivers and the real-life hurdles faced by PROC patients and their caregivers. The outputs of this study will help better understand the hurdles and challenges they face and the significant unmet medical need.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 4, 2025
CompletedFirst Posted
Study publicly available on registry
June 24, 2025
CompletedStudy Start
First participant enrolled
July 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2026
ExpectedDecember 23, 2025
December 1, 2025
10 months
June 4, 2025
December 22, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
To estimate the quality of life of patient with ovarian cancer
Using the the Functional Assessment of Cancer Therapy - Ovarian (FACT-O) and EuroQol 5-dimendion 5-level (EQ-5D-5L)
At recruitment
Secondary Outcomes (4)
Patient's symptoms assessment
At recruitment
Caregiver's Quality of Life
At recruitment
Patients and caregivers work productivity loss and activity impairment
At recruitment
Patient's preference in treatment
At recruitment
Study Arms (2)
Patients with PROC part of Ovarian Cancer Canada mailing lists
Caregiver of PROC patients part of Ovarian Cancer Canada mailing lists
Interventions
No specific intervention is assess in this study.
Eligibility Criteria
Patients with ovarian cancer and caregivers of patients with ovarian cancer who are part Ovarian Cancer Canada mailing list.
You may qualify if:
- ≥18 years old
- Patients with PROC who received \>1 prior line of therapy identified through a screening survey. PROC will be defined as recurrence less than 6 months after last platinum chemotherapy (i.e. carboplatin or cisplatin)
- Ability to read and understand French or English
- Signature of ICF
You may not qualify if:
- Patients with PSOC, defined as those who:
- Have not progressed within less than 6 months after completion of platinum-based chemotherapy or;
- Are still on platinum chemotherapy or;
- Receive maintenance therapy.
- Patients with platinum-refractory ovarian cancer, defined as not responding or disease progressing during therapy or within three months after the last dose
- ≥18 years old
- Current caregiver of a patient with PROC (see definition to be used above) who received \>1 prior line of therapy identified through a screening survey.
- Ability to read and understand French or English
- Signature of ICF.
- Caregivers of patients with PSOC (see definition above)
- Caregivers of PROC patients who have passed away
- Caregivers of platinum-refractory patients (see definition above)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- PeriPharmlead
Study Sites (1)
PROxy Network, an initiative of PeriPharm Inc.
Montreal, Quebec, H2Y 1V3, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 4, 2025
First Posted
June 24, 2025
Study Start
July 15, 2025
Primary Completion
May 1, 2026
Study Completion (Estimated)
June 1, 2026
Last Updated
December 23, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share