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Multidimensional Analysis of Upper Limb Function in Breast Cancer Patients and Efficacy Study of Digital Therapeutic Intervention

Multidimensional Analysis of Upper Limb Function in Breast Cancer Patients and Efficacy Study of Digital Therapeutic Intervention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108524
Enrollment
Unknown
Registered
2025-09-01
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Breast cancer

Interventions

Routine Intervention Group:Based on conventional rehabilitation, implement more standardized exercise training according to the assessment results from digital sensing devices.
Control group:Provide rehabilitation care following standard protocols for breast cancer patients, and offer exercise guidance based on routine rehabilitation training prescriptions.

Sponsors

Huashan Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. 18 years old< = age< = 75 years old; 2. Meet the diagnostic criteria of breast cancer, undergo mastectomy, total breast cancer resection, modified radical breast cancer surgery, breast cancer breast conserving surgery, parallel axillary lymph node dissection or sentinel lymph node biopsy; 3. Breast cancer is the first and unilateral onset; 4. Constant-murley shoulder function score less than 80 points; 5. Stable vital signs and clear consciousness; 6. Be able to contact by yourself or by the Internet or telephone with the assistance of family members; 7. Signed informed consent and voluntarily participated in this research.

Exclusion criteria

Exclusion criteria: 1. Presence of any disease or symptom that may aggravate or cause adverse effects of exercise; 2. Poor compliance of study participants, affecting the determination of efficacy and safety 3. Patients who refuse to sign the informed consent form. 4. Subjects voluntarily withdraw from the trial for any reason.

Design outcomes

Primary

MeasureTime frame
Constant-Murley shoulder scoring scale;

Secondary

MeasureTime frame
QuickDASH;Numerical rating scale;Generalized AnxietyDisorder-7;Patient Health Questionnaire;Brief Fatigue Inventory-Chinese;The Pittsburgh Sleep Quality index;FACT-B(V4.0);

Countries

China

Contacts

Public ContactJia Jie

Huashan Hospital affiliated to Fudan University

shannonjj@126.com+86 136 1172 2357

Outcome results

None listed

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