NCT07035067

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
1mo left

Started Jul 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress92%
Jul 2025Jun 2026

First Submitted

Initial submission to the registry

June 4, 2025

Completed
20 days until next milestone

First Posted

Study publicly available on registry

June 24, 2025

Completed
21 days until next milestone

Study Start

First participant enrolled

July 15, 2025

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

December 23, 2025

Status Verified

December 1, 2025

Enrollment Period

10 months

First QC Date

June 4, 2025

Last Update Submit

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

Other: No intervention

Caregiver of PROC patients part of Ovarian Cancer Canada mailing lists

Other: No intervention

Interventions

No specific intervention is assess in this study.

Caregiver of PROC patients part of Ovarian Cancer Canada mailing listsPatients with PROC part of Ovarian Cancer Canada mailing lists

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

PROxy Network, an initiative of PeriPharm Inc.

Montreal, Quebec, H2Y 1V3, Canada

Location

MeSH Terms

Conditions

Ovarian NeoplasmsCaregiver Burden

Condition Hierarchy (Ancestors)

Endocrine Gland NeoplasmsNeoplasms by SiteNeoplasmsOvarian DiseasesAdnexal DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Neoplasms, FemaleUrogenital NeoplasmsGenital DiseasesEndocrine System DiseasesGonadal DisordersStress, PsychologicalBehavioral SymptomsBehavior

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

Locations