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Construction and preliminary application of self-advocacy intervention program for post-operative cervical cancer patients based on empowerment theory

Construction and preliminary application of self-advocacy intervention program for post-operative cervical cancer patients based on empowerment theory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104428
Enrollment
Unknown
Registered
2025-06-17
Start date
2025-06-17
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Cervical cancer

Interventions

Experimental group:The first draft of the program includes 5 first-level indicators, 10 second-level indicators, and 31 third-level indicators, including assessing the patients situation, helping to f
Control group:Usual care

Sponsors

The Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Comply with the "2024 NCCN Clinical Practice Guidelines for Cervical Cancer (1st Edition)", and be diagnosed as primary cervical cancer by histopathology; 2. Undergo open or laparoscopic radical hysterectomy pelvic lymph node dissection; 3. Age>=18 years; 4. Normal comprehension and communication skills; 5. Have normal reading and writing and cognitive skills, and be able to use WeChat; 6. Patients have informed consent and voluntary participation.

Exclusion criteria

Exclusion criteria: 1. Coexisting with other serious physical diseases; 2. Presence of cognitive impairment or psychiatric disorder; 3. Participation in other interventional studies.

Design outcomes

Primary

MeasureTime frame
Self-advocacy;Social supports;

Secondary

MeasureTime frame
Self efficacy;

Countries

China

Contacts

Public ContactJu Mei

The Affiliated Hospital of Southwest Medical University; School of Nursing, Southwest Medical University

2481476831@qq.com+86 189 0908 7186

Outcome results

None listed

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