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Multidimensional Burden of Platinum Resistant Ovarian Cancer (PROC) on Patients and Caregivers in Canada

Multidimensional Burden of Platinum Resistant Ovarian Cancer (PROC) on Patients and Caregivers in Canada

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07035067
Enrollment
24
Registered
2025-06-24
Start date
2025-07-15
Completion date
2026-04-01
Last updated
2026-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caregiver Burden, Ovarian Cancer, Patient Burden

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.

Interventions

OTHERNo intervention

No specific intervention is assess in this study.

Sponsors

PeriPharm
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patient Inclusion Criteria 1. ≥18 years old 2. 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) 3. Ability to read and understand French or English 4. Signature of ICF Patients

Exclusion criteria

1. Patients with PSOC, defined as those who: 1. Have not progressed within less than 6 months after completion of platinum-based chemotherapy or; 2. Are still on platinum chemotherapy or; 3. Receive maintenance therapy. 2. Patients with platinum-refractory ovarian cancer, defined as not responding or disease progressing during therapy or within three months after the last dose Caregivers Inclusion Criteria: 1. ≥18 years old 2. 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. 3. Ability to read and understand French or English 4. Signature of ICF. Caregivers

Design outcomes

Primary

MeasureTime frameDescription
To estimate the quality of life of patient with ovarian cancerAt recruitmentUsing the the Functional Assessment of Cancer Therapy - Ovarian (FACT-O) and EuroQol 5-dimendion 5-level (EQ-5D-5L)

Secondary

MeasureTime frameDescription
Patient's symptoms assessmentAt recruitmentUsing the Measure of Ovarian Symptoms and Treatment (MOST-T24 (V2))
Caregiver's Quality of LifeAt recruitmentUsing the CareGiver Oncology Quality of Life (CarGOQoL) questionnaire
Patients and caregivers work productivity loss and activity impairmentAt recruitmentUsing the Work Productivity and Activity Impairment (WPAI) questionnaire
Patient's preference in treatmentAt recruitmentUsing a questionnaire specifically developed for this study based on a literature search, physician input and patient association input.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 8, 2026