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Development and Preliminary Application of a Post-Traumatic Growth Intervention Program for Breast Cancer Patients Undergoing Postoperative Chemotherapy and Their Spousal Caregivers

Development and Preliminary Application of a Post-Traumatic Growth Intervention Program for Breast Cancer Patients and Their Spousal Caregivers

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124395
Enrollment
Unknown
Registered
2026-05-12
Start date
2026-05-12
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Breast cancer

Interventions

Intervention group:Provide psychological intervention programs in addition to routine care
Observation group:Provides only routine care
Observation study population (cross-sectional):No intervention
questionnaire survey only
Observation study population (qualitative interviews):No intervention
face-to-face interviews only

Sponsors

Affiliated Hospital of Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with a pathological diagnosis of breast cancer whose condition is stable, and their spouses who, as identified by the patients, are primarily responsible for their care; 2. Patients undergoing their first course of chemotherapy following breast surgery; 3. Married patients living with their spouses, both of whom possess basic reading, comprehension, and writing skills; 4. Both parties have provided informed consent and voluntarily agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with other serious comorbidities, such as heart failure or impaired liver or kidney function; 2. Patients with mental disorders that prevent normal communication; 3. Divorced or widowed patients; 4. Breast cancer patients who were lost to follow-up or withdrew from the study; 5. Patients who have already participated in other clinical psychological trials.

Design outcomes

Primary

MeasureTime frame
Post-Traumatic Growth;Dyadic coping;Meaning in life;Rumination;Anxiety and Depression;Perceived social support;

Countries

China

Contacts

Public ContactZhao Jie

Affiliated Hospital of Jiangnan University

1014857395@qq.com+86 138 6187 6828

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026