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Construction and application of a family participatory surgical decision-making aid program for early-stage breast cancer patients

Construction and application of a family participatory surgical decision-making aid program for early-stage breast cancer patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084835
Enrollment
Unknown
Registered
2024-05-27
Start date
2024-05-29
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

breast cancer

Interventions

Experimental group (paired):Applying a family-participatory surgical decision-making assistance program for patients with early-stage breast cancer + Routine Nursing Care Education
Control group (paired):Routine Nursing Care Education

Sponsors

Fujian Medical University Union Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients: ? breast cancer patients with pathological diagnosis of stage I-II ; ? female, age =18 years old; ? meeting the indications for surgery, agreeing with the doctor on elective surgery, and facing the decision of surgical modality; ? stable condition and knowing the diagnosis. Family members: ? are related to the patient (spouse, parents, children, direct or collateral siblings); ? are =18 years old; ? are aware of the patient's disease diagnosis, condition, and treatment; ? have complete verbal expression and comprehension.

Exclusion criteria

Exclusion criteria: Patients: ? have had previous surgery related to breast cancer; ? have pending medical disputes; ? have a history of cognitive impairment or other mental illnesses, severe visual, auditory, or speech disorders; ? have terminal malignant tumors and other major organs (e.g., liver, kidney) with severe damage; ? have participated or are participating in other similar studies; Family members: (i) previous or current psychological problems; (ii) history of cognitive disorders, dementia or mental illness; (iii) have participated or are participating in other similar studies;

Design outcomes

Primary

MeasureTime frame
Decisional Conflict;

Secondary

MeasureTime frame
Preparation Decision Making;Satisfaction with decision-making;Decision Regret;Family Adapt ability and Cohesion;Anxiety and depression;

Countries

China

Contacts

Public ContactWu Hangzhou

Fujian Medical University Union Hospital

13365910632@163.com+86 133 6591 0632

Outcome results

None listed

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