E-Health Portal for Individualized Treatment Monitoring and Patient Engagement in Oncology Research

University Hospital Tuebingen106 enrolled

Overview

Evaluation of patient acceptance and characterization of response behaviour for web-based compared with respective paperbacked patient reported outcomes.

Paperbacked pPRO data from up to a total of 100 patients from the cohort of PRAEGNANT are planned to be included in the Pepper I PRO study. Additionally 200 patients will be recruited in the web based ePRO cohort. The study duration per patient is at least 8 weeks. In cases of stable disease the study duration can be extended to up to 6 months with monthly PRO assessments, according to the attached visit matrix, taking approximately 20 minutes per visit. The documentation at baseline should be performed during clinical routine with trained study personnel followed by remote self-reporting to minimize the patient effort. Pepper I will be conducted as sub-protocol of the PRAEGNANT trial.

Study Type

OBSERVATIONAL

Enrollment

106

Conditions

Breast Cancer Metastatic

Interventions

patient-reported-outcomesOTHER

Explorative pilot study combining collected data from the PRAEGNANT study on paper-based patient-reported-outcomes with additional collected data on web-based patient-reported-outcomes

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients enrolled in PRAEGNANT * Women aged ≥18 years * Patients with the diagnosis metastasized breast cancer undergoing any form of systemic therapy * Patients who are willing and able to sign the informed consent form * Patients with therapy change Exclusion Criteria: * Patients who are not eligible for observation due to severe comorbidities or unavailability according to the treating physician * Patients who are not able to handle a tablet computer or are unable to write * Patients who are not able to understand the nature and extent of the trial and the procedures require

Locations (1)

Department for Women's Health

Tübingen, Germany

Outcomes

Primary Outcomes

QLQ-C30 questionnaire for baseline

Overall patient completion rate in the paperbacked questionnaire and the web-tool, respectively

Time frame: 8 weeks