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Construction of self-advocacy intervention program for female patients with colorectal cancer

Construction of self-advocacy intervention program for female patients with colorectal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098108
Enrollment
Unknown
Registered
2025-03-03
Start date
2024-01-01
Completion date
Unknown
Last updated
2025-03-10

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

Conditions

Colorectal cancer

Interventions

Intervention group:Empowerment theory behavioral intervention+routine nursing
Control group:Routine nursing

Sponsors

The Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Mixed studies: 1. Clear mind, >=18 years old; 2. Patients diagnosed with primary colorectal cancer by clinicopathological examination; 3. Female patients; 4. First admission and completed surgical treatment; 5. Able to communicate effectively and read; 6. Informed consent and voluntary participation in this study Intervention studies: 1. Conscious female patients >=18 years old; 2. Patients diagnosed with primary colorectal cancer by clinicopathological examination; 3. First admission and planned surgical treatment; 4. Able to communicate normally and read; 5. Master the basic operation of electronic equipment; 6. Informed consent and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: Mixed research: 1.Patients with psychiatric history, cognitive impairment and communication disorders; 2.Complicated with other malignant tumors; 3.Those suffering from infectious diseases or physical disabilities. Intervention study: 1.Patients with psychiatric history, cognitive impairment and communication disorders; 2.Complicated with other malignant tumors; 3.Receiving other cancer treatment (neoadjuvant chemotherapy, radiotherapy or targeted therapy) before surgery; 4.Is participating in other studies.

Design outcomes

Primary

MeasureTime frame
Self-advocacy;

Secondary

MeasureTime frame
Social Support;Sense of stigma;

Countries

China

Contacts

Public ContactLi Xianrong

the Affiliated Hospital of Southwest Medical University

237239891@qq.com+86 152 9825 6287

Outcome results

None listed

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