Breast Cancer
Conditions
Interventions
Intervention group:Access to a WeChat-based digital intervention program, including information modules, peer discussion forums, intelligent content recommendations, and regular online follow-up for y
Control group:Access to the information module of the WeChat applet only, without intelligent recommendations, peer forums, or regular online follow-up.
Sponsors
Renji Hospital, Shanghai Jiao Tong University School of Medicine
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Young breast cancer survivors(YBCSs): 1. Women aged 18-45; 2. Diagnosed as breast cancer, pathological stage I - III; 3. Ability to access the Internet using a computer or other mobile device; 4. Have a certain level of education and comprehension, and be able to complete online questionnaires and interviews independently; 5. Fully informed consent and voluntary participation. Family caregivers: 1. A family member or recognized primary caregiver of the patient; 2. Over 18 years old; 3. Ability to access the Internet using a computer or other mobile device; 4. Ensure that ongoing emotional and/or substantive support can be provided to YBCSs; 5. Fully informed consent and voluntary participation.
Exclusion criteria
Exclusion criteria: Young breast cancer survivors: 1. History of severe mental illness (including severe mental disorders, major depression, etc.), history of neurological disorders (including dementia, stroke, Parkinson's disease, etc.), history of acute or severe illness, alcohol or drug addiction; 2. Has participated in other similar auxiliary support projects; 3. Loss of follow-up and voluntary withdrawal during the study; 4.Individuals who lack legal capacity or have limited legal capacity. Family caregivers: 1. History of severe mental illness (including severe mental disorders, major depression, etc.), history of neurological disorders (including dementia, stroke, Parkinson's disease, etc.), history of acute or severe illness, alcohol or drug addiction; 2. Has participated in other similar auxiliary support projects; 3. Loss of follow-up and voluntary withdrawal during the study; 4. Work in related care professions, e.g. carers, nannies, etc; 5.Individuals who lack legal capacity or have limited legal capacity.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Symptoms of YBCSs causing trouble;Supportive Care Needs; | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life;Family resilience;Self-efficacy; | — |
Countries
China
Contacts
Public ContactXu Jiehui
Renji Hospital, Shanghai Jiao Tong University School of Medicine
Outcome results
None listed