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A cohort study of quality of life in breast cancer patients based on patient-reported outcomes (PRO)

A cohort study of quality of life in breast cancer patients based on patient-reported outcomes (PRO)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102098
Enrollment
Unknown
Registered
2025-05-08
Start date
2024-06-11
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Breast cancer

Interventions

Sponsors

Suining Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Breast cancer survivor inclusion criteria: complete surgery with or without adjuvant radiation and/or chemotherapy and surgery and survival over three months; female; age: >18 years old; sign informed consent to participate in this study voluntarily. 2.Inclusion criteria for newly diagnosed breast cancer patients: breast cancer patients confirmed by pathology; female; age: >18 year old; signed the informed consent form and volunteered to participate in this research.

Exclusion criteria

Exclusion criteria: 1.Those who cannot complete the scale independently due to serious audio-visual impairment, low reading ability or other reasons; 2.Patients who are critically ill and physically unable to cooperate with the investigation; 3.Suffering from major mental illness or unable to understand the research content; 4.Patients with other malignant tumors.

Design outcomes

Primary

MeasureTime frame
Quality of life;

Secondary

MeasureTime frame
Patient-reported outcomes;Generalized anxiety disorder;Functional status of shoulder joint;Patient-reported symptoms;

Countries

??

Contacts

Public ContactChen Maoshan

Suining Central Hospital

snscms@126.com+86 180 0825 5330

Outcome results

None listed

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