Patient Education Strategy for Breast Cancer Patients During Perioperative Hospitalization Stage

NCT ID: NCT06965556

Last Updated: 2025-05-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

1138 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-01

Study Completion Date

2026-10-31

Brief Summary

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Introduction Breast cancer remains a leading global health concern, with significant psychological challenges during the perioperative period. Traditional patient education focuses on disease management but often neglects emotional and cognitive needs. Perioperative inpatients are relatively stable and have the time and mental space for deeper education and psychological support. This study evaluates the clinical significance of a medical humanities-based education strategy for breast cancer patients during hospitalization, aiming to enhance psychological resilience, treatment adherence, and quality of life.

Methods and Analysis This prospective, non-randomized, open-label study will include female patients with early-stage breast cancer scheduled for surgery at Fudan University Shanghai Cancer Center. Participants will be allocated to two cohorts: practical education group and mental enhanced group. The primary endpoint is psychological assessment at hospital discharge, including anxiety (GAD-7), depression (PHQ-9), and sleep quality (ISI). Secondary endpoints include the proportion of patients opting for breast-conserving procedures, incidence of postoperative complications, long-term treatment adherence (MMAS-8), patients' disease-coping resilience (CD-RISC-10), and quality of life assessment (EORTC QLQ instruments) at 12-month follow-up. Data collection and statistical analysis will be conducted using validated instruments and software, with significance set at p ≤0.05.

Ethics and Dissemination Approved by the FUSCC ethics committee, all participants provide informed consent. Results will be disseminated through international conferences and peer-reviewed journals. The study adheres to ethical guidelines, ensuring data confidentiality via encrypted platforms. Authors declare no conflicts of interest, supported by Shanghai Municipal Science and Technology Innovation Action Plan (24DZ2303500). Findings aim to optimize perioperative education strategies, addressing psychological and informational needs of breast cancer patients.

Detailed Description

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Conditions

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Breast Carcinoma Patient Education Perioperative Care Psychological Intervention

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Medical Humanities-based Patient Education Strategy

Mental Enhanced Education Strategy

Patients allocated to the enhanced mental health education intervention cohort will receive supplemental medical humanities modules alongside the standard Practical Education Strategy during hospitalization. This content is derived from a comic publication compiled by the breast surgery team of Fudan University Shanghai Cancer Center, which narrates the 4600-year human battle against breast cancer in a grand story. The content combines humorous cartoons with novel-like text, covering the evolution of human understanding of breast cancer, and the emergence and development of various therapies, drugs, and technologies. For patients unable to read, audio books and dynamic cartoon videos are available on mobile devices. The general content framework is as follows:

* Understanding of breast cancer in ancient Egypt and Persia;
* Hippocratic-Galenic Theories: early management of breast disorders in Greco-Roman antiquity;
* Traditional Chinese medical interpret

Group Type ACTIVE_COMPARATOR

Medical Humanities-based Patient Education Strategy

Intervention Type OTHER

Medical Humanities-based Patient Education with Comic-based Medical Education Materials for Breast Cancer Patients during Perioperative Hospitalization Stage

Routine Patient Education Strategy

Practical Education Strategy

Admission Day

* Comprehensive admission nursing assessment and introduction to care protocols: Admission assessment form, nutritional assessment, fall risk assessment, deep vein thrombosis risk assessment, pain assessment, etc.
* Orientation to ward environment and policies: introduction to the medical team, online doctor-patient communication platform, ward facilities, daily routines, dietary guidelines, and other essential services, etc.
* Review of medical history and guidance on preoperative examinations and precautions: Hematological tests, electrocardiogram, ultrasound, mammography, CT, MRI, core needle biopsy, fine needle aspiration, etc.

Days Before Surgery

* Personal preparation instructions: Bathing, hair washing, fasting, and fluid restriction guidelines, etc.
* Interpretation of preoperative examination results.
* Overview of common surgical approaches for breast cancer, introduction of surgery options based on the condition, especially emphasis on

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Medical Humanities-based Patient Education Strategy

Medical Humanities-based Patient Education with Comic-based Medical Education Materials for Breast Cancer Patients during Perioperative Hospitalization Stage

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* More than 18 years old
* Female
* Patient with early-stage breast cancer with preoperative pathology confirming invasive breast carcinoma or ductal carcinoma in situ
* No clinical or imaging evidence of distant metastasis
* Patients to receive breast surgery during hospitalizaiton (including mastectomy, breast conserving therapy, reconstrucion, etc.)
* Be able and willing to sign the Informed Consent Form (ICF)

Exclusion Criteria

* Patients with locally advanced breast cancer to receive neoadjuvant therapy
* Patients currently participating in other clinical trials, which may have impact on the participation in this trial
* Previous history of breast cancer (patients with ipsilateral recurrence after breast sparing surgery)
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Fudan University

OTHER

Sponsor Role lead

Responsible Party

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Jiong Wu

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Fudan University Shanghai Cancer Center

Shanghai, , China

Site Status

Countries

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China

Central Contacts

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Jiajian Chen, MD

Role: CONTACT

862164175590

Facility Contacts

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Jiajian Chen, MD

Role: primary

+8618221810450

Other Identifiers

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PE-CAT

Identifier Type: -

Identifier Source: org_study_id

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