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Construction and application of a walking exercise intervention program for breast cancer patients undergoing postoperative chemotherapy based on social cognitive theory

Construction and application of a walking exercise intervention program for breast cancer patients undergoing postoperative chemotherapy based on social cognitive theory

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127984
Enrollment
Unknown
Registered
2026-07-11
Start date
2026-06-18
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Brest cancer

Interventions

Control group:The control group received routine nursing intervention. They were given fitness wristbands and advised to engage in walking exercises, with the data recorded and exported on a weekly ba
Intervention group:The intervention group implemented a walking exercise intervention program based on the social cognitive theory on the basis of routine care. Before the first chemotherapy session f

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. Pathological diagnosis of primary breast cancer; 3. First chemotherapy received after surgery, and the chemotherapy course is >= 6 cycles; 4. Good physical condition, Eastern Cooperative Oncology Group physical status score <= 1, and no exercise contraindications; 5. Informed and voluntarily participating in this study, able to use the activity monitor normally, and able to complete the questionnaire independently or under the guidance of the researcher.

Exclusion criteria

Exclusion criteria: 1. Merge diseases such as severe heart, lung, liver and kidney dysfunction that may increase the risk of exercise; 2. Have severe cognitive impairment or mental disorders, and are unable to understand the research content or provide informed consent; 3. Have mental disorders or cognitive impairments and are unable to understand this study; 4. Have a regular exercise habit (having engaged in at least 3 days per week, each lasting at least 30 minutes of moderate-intensity exercise in the past 3 months); 5. Are simultaneously participating in other interventional clinical studies that affect the outcome of this research.

Design outcomes

Primary

MeasureTime frame
Quality of life;

Secondary

MeasureTime frame
Cancer-related fatigue;Exercise compliance;Exercise Self-Efficacy;Outcome Expectations for Exercise;Social support;30-Second Sit-to-Stand Test;

Countries

China

Contacts

Public ContactShunLi Xu

The First Affiliated Hospital of Guangxi Medical University

1909465607@qq.com+86 771 535 9553

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026