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The Possible Influence of Different Follow-up Modalities on Overall Survival in Ovarian Cancer (ECOvar)

S

Stiftung Swiss Tumor Institute

Status

Terminated

Conditions

Ovarian Neoplasms
Patient Reported Outcome Measures

Treatments

Device: Mobile app ovarian cancer followup (ePRO)

Study type

Observational

Funder types

Other

Identifiers

NCT05352217
2021-D0052

Details and patient eligibility

About

The study is designed as an observational cohort study, aiming to evaluate, whether a structured recording of symptoms by a mobile app contributes insight in the follow-up modalities of ovarian cancer patients.

Full description

The observational study will examine different follow-up modalities for ovarian cancer patients with the ultimate goal of improving follow-up strategies for an improved well-being and better clinical outcomes. The primary objective is to quantify the effects of conservative clinical diagnostics by collecting symptoms via ePRO in addition to intensive diagnostics (CA-125 testing, imaging diagnostics) during follow-up, on survival, time to clinical recurrence and well-being.

Enrollment

7 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women aged ≥ 18 years
  • Between diagnosis and the first follow-up visit after the end of their antineoplastic treatment (systemic therapy or surgical treatment) for ovarian cancer.
  • German, English, French, or Italian speaking
  • Personal smartphone (iOS or Android system); one of the latest three main versions

Exclusion criteria

• Patients whose compliance must be questioned, e.g. due to a psychiatric disorder, private life situation or insufficient knowledge on smartphone use and do not have a suitable caregiver to assist them with symptom reporting.

Trial contacts and locations

4

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Central trial contact

Andreas Trojan, Prof.Dr.med

Data sourced from clinicaltrials.gov

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