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Development and Preliminary Application of an Emotional Suppression Intervention Program for Breast Cancer Patients Based on Spousal Support

Development and Preliminary Application of a Spouse-Supported Emotional Inhibition Intervention Protocol for Breast Cancer Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116023
Enrollment
Unknown
Registered
2026-01-04
Start date
2025-08-05
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Brest neoplasm

Interventions

Experimental group:On the basis of routine health education for patients in the control group, a spouse-based emotional suppression intervention was administered to brea
Control group:1. Health Education: The responsible nurse provided patients with information about the medications used and precautions during medication administration, instructed patients on treatmen

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Patient Inclusion Criteria:(1)Married female patients aged 20 years or older,the study participants' spouses were adults; (2)Diagnosed with breast cancer by clinical pathology and receiving chemotherapy (including neoadjuvant chemotherapy patients); (3)Informed consent obtained from the patient, with a signed informed consent form; (4)Patients must be conscious, aware of their own condition, have no barriers to verbal communication, and be able to complete questionnaires independently or with the assistance of researchers.

Exclusion criteria

Exclusion criteria: Patient Inclusion Criteria: (1)Patients with advanced malignant cancer and poor prognosis; (2)Patients with cancer recurrence or distant metastasis; (3)Patients experiencing rapid disease progression or complicated by other severe physical illnesses; (4)Patients with severe psychiatric or language dysfunction; (5)Patients currently participating in or with a history of participation in similar studies.

Design outcomes

Primary

MeasureTime frame
Emotional Suppression;

Secondary

MeasureTime frame
Self-management;Social support;

Countries

China

Contacts

Public ContactTieying Shi

The First Affiliated Hospital of Dalian Medical University

Sty11177@163.com+86 411 8363 3415

Outcome results

None listed

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