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The family synchronous education model based on the IMB model improves the pain awareness and self-management ability of elderly gastric cancer patients during the perioperative period

Research on the application of family synchronous education model based on IMB model in perioperative pain management of elderly patients with gastric cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092711
Enrollment
Unknown
Registered
2024-11-21
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Gastric cancer, pain

Interventions

Control group:At the time of admission, one day before surgery, and upon returning to the ward after surgery, researchers provide routine pain health education to patients
Control group:At the time of admission, one day before surgery, and upon returning to the ward after surgery, researchers provide no education to families of thenpatient
Intervention group:At the time of patient admission, one day before surgery, and upon returning to the ward after surgery, researchers provide synchronous pain education for patientsbased on the IMB m
Intervention group:At the time of patient admission, one day before surgery, and upon returning to the ward after surgery, researchers provide synchronous pain education for families of the patient

Sponsors

The First Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Patient inclusion criteria: 1. After gastroscopy examination, the pathological diagnosis is gastric cancer, and gastric cancer radical surgery is scheduled; 2.Age >= 60 years old; 3.No history of mental illness; 4. No cognitive impairment, with language communication ability; 5. Voluntary trial, informed consent form. Family inclusion criteria: 1.Age range from 18 to 60 years old; 2. Being the primary caregiver of patients (providing full care from admission to discharge), occupying a dominant position in the treatment and nursing decisions of patients; 3. No cognitive impairment, with language communication ability; 4. Voluntary trial, informed consent form

Exclusion criteria

Exclusion criteria: Patient exclusion criteria: 1. Individuals with severe visual and auditory impairments; 2. Alcohol abuse, drug abuse, or dependence. Exclusion criteria for family members: 1.Severe hearing or visual impairment; 2.Individuals with combined cognitive or mental disorders;

Design outcomes

Primary

MeasureTime frame
Postoperative pain knowledge and belief scores for surgical patients;Patient's postoperative pain self-management behavioral ability score;

Secondary

MeasureTime frame
Patient's postoperative NRS scores at 0, 4, 8, 12, 24, 48, and 72 hours;Patient satisfaction with pain education;

Countries

China

Contacts

Public ContactXu Huili

The First Affiliated Hospital of Zhejiang University School of Medicine

995797079@qq.com+86 187 5716 0972

Outcome results

None listed

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