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Construction and Validation of a Frailty Intervention Model for Middle-aged and Elderly Breast Cancer Patients Undergoing Chemotherapy Based on Mind-Body Exercise (Baduanjin)

Construction and Validation of a Frailty Intervention Model for Middle-aged and Elderly Breast Cancer Patients Undergoing Chemotherapy Based on Mind-Body Exercise (Baduanjin)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106298
Enrollment
Unknown
Registered
2025-07-22
Start date
2025-08-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

breast cancer

Interventions

intervention group:The intervention group will receive a 12-week progressive home-based Baduanjin exercise intervention. Both the weekly exercise frequency and daily duration will gradually increase o
control group:During the intervention period for the intervention group, the control group will receive routine care

Sponsors

Sun Yat-sen Memorial Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Female patients with a pathological diagnosis of breast cancer; 2. Receive chemotherapy; 3. Aged >=45 and <=70 years; 4. Aware of their cancer diagnosis; 5. Possess basic listening, speaking, reading, and writing skills, and able to complete questionnaires independently or with guidance from an investigator; 6. Willing to participate in the study and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Presence of severe dysfunction of the heart, liver, brain, lungs, or kidneys, or diagnosis of end-stage disease; 2. Patients with recurrent or advanced-stage breast cancer; 3. Individuals who are partially or completely unable to perform self-care (ECOG performance status >=3); 4. Presence of one or more absolute or relative contraindications to exercise (as determined by the interventionist based on relevant guidelines), or any "Yes" response on the Physical Activity Readiness Questionnaire (PAR-Q); 5. History of psychiatric disorders, including those currently taking psychiatric medications or undergoing psychological therapy.

Design outcomes

Primary

MeasureTime frame
Frailty;

Secondary

MeasureTime frame
Balance and Gait Performance;Psychological Well-being;

Countries

China

Contacts

Public ContactJingwen Yan

Sun Yat-sen Memorial Hospital

yanjw6@mail.sysu.edu.cn+86 181 3871 8525

Outcome results

None listed

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