Development and Application of a Parenting Anxiety Intervention Program for Young and Middle-Aged Female Breast Cancer Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Parenting Concerns Support Program.
- Who it may be relevant to
- Registry conditions: Breast Cancer, Parenting Anxiety. Basic parameters: 18 years — 59 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Parenting Concerns of Young and Middle-aged Women With Breast Cancer: A Study Protocol for a Feasibility Trial
Overview
This feasibility study aims to develop and test an intervention program for young and middle-aged female breast cancer patients who experience parenting concerns. Eligible participants will receive the tailored support program (including psychological counseling and parenting guidance). The study will assess whether the program is acceptable, feasible, and potentially helpful in reducing parenting concerns among this group.We plan to enroll 20 participants from Shanghai Zhoupu Hospital between March 2026 and October 2026.
Interventions
- Behavioral Parenting Concerns Support Program
A 6-week program including 2 individual psychological counseling sessions and 4 group parenting guidance activities, designed to reduce parenting concerns in young and middle-aged female breast cancer patients.
Primary outcome measures
- Parenting Concerns Scale for Breast Cancer Patients [Time frame: Baseline (pre-intervention) , 6 weeks post-intervention (end of the program) and One month after the intervention ended]
Secondary outcome measures (2)
- Parenting Sense of Competence Scale [Time frame: Baseline (pre-intervention), 6 weeks post-intervention (end of the program) and One month after the intervention ended]
- Herth hope index [Time frame: Baseline (pre-intervention) , 6 weeks post-intervention (end of the program) and One month after the intervention ended]
Eligibility criteria
Inclusion criteria
- Clear breast cancer patients confirmed by histopathology who have received surgical treatment
- Aged 18 to 59 and currently raising at least one minor child under the age of 18
- Clinical stage I - IV
- Be aware of the condition, provide informed consent and voluntarily participate in this study
- The patient can cooperate with the research independently and has normal reading, comprehension, thinking and judgment abilities
Exclusion criteria
- Concurrent with other cancers
- Engaged in psychology work, or having received psychological intervention guidance within the past six months
- Participate in other nursing intervention studies simultaneously
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07331740 · To be assigned