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A multicenter cross-sectional study of patient-reported outcomes (PRO) in breast cancer survivors

A multicenter cross-sectional study of patient-reported outcomes (PRO) in breast cancer survivors

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097143
Enrollment
Unknown
Registered
2025-02-13
Start date
2025-03-01
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Breast cancer

Interventions

Observation group:None

Sponsors

Suining Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Gender female; 2) Age >=18 years old; 3) Diagnosed with breast cancer by pathology; 4) Patients who have received local surgery and have (new) indications of adjuvant chemoradiotherapy have completed the corresponding treatment, and the disease-free survival time after the completion of treatment is >=6 months; 5) Voluntarily participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1) Recurrent metastatic breast cancer (newly diagnosed stage IV patients); 2) Patients with serious diseases of the heart, liver, kidney and other important organs or mental diseases, which affect the judgment of the study results; 3) Patients with other malignant tumors; 4) Unable to communicate effectively or understand the research content.

Design outcomes

Secondary

MeasureTime frame
Quality of life;Mental Health;Return status;

Primary

MeasureTime frame
Patient-reported outcomes;

Countries

China

Contacts

Public ContactMaoshan Chen

Suining Central Hospital

snscms@126.com+86 180 0825 5330

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026