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Study on the application of ERAS health education model based on 5S management and teach-back method in postoperative rehabilitation of gynaecological malignant tumours

Study on the application of ERAS health education model based on 5S management and teach-back method in postoperative rehabilitation of gynaecological malignant tumours

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098808
Enrollment
Unknown
Registered
2025-03-13
Start date
2025-03-24
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Ovarian, cervical and endometrial cancer

Interventions

Intervention group:Implementation of ERAS health education model based on 5S management and teach-back method for health promotion to subjects
Control group: Routine perioperative health education only

Sponsors

Guizhou Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-75 years old; (2) Patients undergoing elective surgery for gynecological malignant tumors, including all histological subtypes of cervical cancer, endometrial cancer, ovarian cancer, and all patients staging the International Federation of Obstetrics and Gynecology (FIGO); (3) No other malignant tumors; (4) American Society of Anesthesiologists (ASA) health status classification I-III; (5) No severe cardiopulmonary dysfunction before surgery; (6) Those who did not have severe malnutrition and did not need supportive care (NRS> = 3 points, and lost more than 10% of their body weight within 6 months; serum albumin<30 g/L; BMI<18.5kg/?); (7) Good general condition without serious medical and surgical complications; (8) Able to cooperate with questionnaires and follow-up; (9) Patients who may require further radiotherapy or chemotherapy after surgery can also be included, but relevant treatment information should be recorded.

Exclusion criteria

Exclusion criteria: (1) Those who are unable to obtain informed consent; (2) Serious complications of heart, brain, lung, liver, kidney and other organs before surgery; (3) Those with mental disabilities, severe mental illnesses and other cognitive abnormalities who are unable to cooperate; (4) Unplanned secondary surgery.

Design outcomes

Primary

MeasureTime frame
Complication rate within 30 days;—

Secondary

MeasureTime frame
HADS scale ratings;QoR-15 scale ;ERAS compliance rate;Sleep quality;Post-operative recovery time;White blood cell count;Hemoglobin (Hb);Platelet count;Alanine aminotransferase ;Albumin;Prothrombin time;—

Countries

China

Contacts

Public ContactZi Dan

Guizhou Provincial People's Hospital

2816497455@qq.com+86 139 0851 9916

Outcome results

None listed

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