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National Baseline Assessment of Breast Cancer Rehabilitation and the Construction of a Standardized Rehabilitation Pathway

National Baseline Assessment of Breast Cancer Rehabilitation and the Construction of a Standardized Rehabilitation Pathway

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099665
Enrollment
Unknown
Registered
2025-03-27
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Fitness, cognitive, psychological, sleep, and pain dysfunction in breast cancer patients

Interventions

Case series:None

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 75 years old. 2. Diagnosed with breast cancer by pathology and histology, and in accordance with the recognized diagnostic standards of the Chinese Anti-Cancer Association (CACA) Guidelines and Standards for the Diagnosis and Treatment of Breast Cancer. Guidelines and Criteria for Breast Cancer Diagnosis and Treatment of the Chinese Anti-Cancer Society. 3. Participants are physically fit to participate in the baseline assessment of rehabilitation, and do not have serious heart, liver, kidney and other important organ dysfunctions. 4. Voluntarily participate in the study, sign the informed consent form, and understand the purpose, procedures and possible risks of the study. 5. Have good cognitive function and be able to cooperate in completing the questionnaires and assessments related to the study.

Exclusion criteria

Exclusion criteria: 1. Have other malignant tumors or serious illnesses that may interfere with the baseline assessment for rehabilitation. 2. Have a history of mental illness or severe cognitive impairment. 3. Is unable to cooperate in completing study-related questionnaires and assessments. 4. Have participated in other clinical studies within the past period of time and have not met the required washout period.

Design outcomes

Primary

MeasureTime frame
Sit to Stand Performance;Handgrip strength test;QuickDASH;FACT-Cog (Version 3);Montreal Cognitive Assessment Basic Scale, MoCA;Generalized Anxiety Disorder Assessment, GAD-7;Patient Health Questionnaire-9, PHQ-9;Pittsburgh Sleep Quality Index, PSQI;Pain Catastrophization Scale, PCS;Symptom Checklist-90;

Countries

China

Contacts

Public ContactJie Jia

Huashan Hospital, Fudan University

shannonjj@126.com+86 21 52887820

Outcome results

None listed

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