Fathers and Mothers Invested in Lives of Their Youth (FAMILY) Study: A Pilot Intervention

UNC Lineberger Comprehensive Cancer Center

Status

Terminated

Conditions

Parenting

Metastatic Breast Cancer

Treatments

Behavioral: FAMILY Intervention

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT04092816

5K07CA218167-02 (U.S. NIH Grant/Contract)

LCCC1920

Details and patient eligibility

About

This is a single-arm pilot study to evaluate the feasibility and acceptability of a novel psychosocial intervention to improve psychosocial outcomes for parents with advanced cancer and their co-parents. In this single-center study, we will recruit ten mothers with metastatic breast cancer and their co-parents as dyads (N=20) to participate in the Fathers and Mothers Invested in the Lives of their Youth (FAMILY) intervention. Patient and co-parent dyads will participate in 2-3 study visits with an intervention facilitator and a post-intervention feedback interview. Participants will also complete baseline and follow-up study surveys. The final products of this study will be the FAMILY intervention manual and training materials, and fidelity assessments.

Full description

Cancer is the leading disease-specific cause of early parental death in the United States and having dependent children worsens suffering for parents with advanced cancer and their families. The FAMILY intervention consists of manualized visits with a trained intervention facilitator and psychoeducation materials to help parents cope with cancer-related parenting concerns. The purpose of the intervention is to improve parenting concerns, emotional well-being, and end-of-life (EOL) preparation among participants. This study will evaluate whether a psychosocial intervention to reduce psychological distress and improve EOL preparation for mothers with metastatic breast cancer and their co-parents can be acceptable, feasible, and relevant to the target patient population.

This study is needed in order to generate critical data to: (1) refine the intervention in preparation for a pilot efficacy randomized controlled trial (RCT); and to generate preliminary data demonstrating the feasibility and acceptability of core intervention components. The preliminary data will support future grant applications for a full-scale efficacy RCT.

Enrollment

15 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for patients:

Be a woman with metastatic (stage IV) breast cancer who has either: (1) estrogen (ER), progesterone (PR), or HER2 receptor-negative cancer and disease progression beyond first line of therapy, or (2) ER, PR, or HER2 -positive cancer and disease progression beyond two lines of therapy;
A mother of at least one dependent child, defined as a child <18 years of age who lives at least half-time in the home;
Be at least 18 years of age;
Adequate stamina to complete at least two study visits
Able to provide informed consent
Able to complete all study measures and visits in English;
Be willing to participate in study visits at the North Carolina Cancer Hospital (NCCH) if they live >75 miles away from NCCH
Have an identified co-parent who is eligible and willing to participate in the study.

Inclusion Criteria for Co-parents:

Be an adult man or woman who is both a partners or spouse of the patient and who would serve as the child(ren)'s primary caregiver if the patient were to become unavailable;
Able to provide informed consent;
Able to complete all study measures and visits in English;
Stated willingness to comply with all study procedures; and
Be at least 18 years of age.

Exclusion Criteria for patients and co-parents:

Unable to participate in study visits due to illiteracy, inability to speak English or other causes.
Live more than 75-miles away from the North Carolina Cancer Hospital (NCCH) and unable to attend study visits at NCCH (participants who live more than 75-miles away and can attend study visits at NCCH remain eligible for participation).
Unwilling to be audio-recorded during facilitated study visits and feedback interview.