Development and Application of a Parenting Anxiety Intervention Program for Young and Middle-Aged Female Breast Cancer Patients

NCT ID: NCT07331740

Last Updated: 2026-01-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2026-03-01

Study Completion Date

2026-12-01

Brief Summary

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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.

Detailed Description

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Conditions

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Breast Cancer Parenting Anxiety

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

This is a single-arm feasibility trial; all eligible participants receive the parenting anxiety intervention program.
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Parenting Concerns Intervention Group

All eligible participants will receive the tailored parenting concerns intervention program.

Group Type EXPERIMENTAL

Parenting Concerns Support Program

Intervention Type BEHAVIORAL

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.

Interventions

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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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

59 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Shanghai University of Traditional Chinese Medicine

OTHER

Sponsor Role lead

Responsible Party

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Hu Hanqi

Master's Student, School of Nursing, Shanghai University of Traditional Chinese Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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To be assigned

Identifier Type: -

Identifier Source: org_study_id

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