Enhancing Connections Program in Improving Family Adjustment in Patients With Incurable Cancer

Fred Hutchinson Cancer Center (FHCC)

Status

Terminated

Conditions

Advanced Malignant Neoplasm

Treatments

Other: Communication Intervention

Other: Questionnaire Administration

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT03049397

NCI-2016-01640 (Registry Identifier)

RG9218011 (Other Identifier)

P30CA015704 (U.S. NIH Grant/Contract)

9667 (Other Identifier)

Details and patient eligibility

About

This pilot clinical trial studies how well the Enhancing Connections program improves family adjustment in patients with incurable cancer. Participating in an educational program with a co-parent to learn about ways to talk to a child about cancer may help parents and co-parents support their child with the parent's cancer and may help families communicate and function better.

Full description

PRIMARY OBJECTIVES:

I. Test the feasibility of the study protocol in advanced cancer patients and co-parents (recruitment/retention, dosage and fidelity of the intervention; program acceptability of program; and logistics).

II. Evaluate the short-term impact of the program on the diagnosed parents', co-parents' and children's adjustment and family functioning using a within group design (pre- and posttest design).

III. Compare outcomes from the Enhancing Connections Palliative Program with similar outcomes obtained from the completed phase III trial (between group design) for the patients and children outcomes.

IV. Evaluate the longer term impact of the program on the co-parents' and children's adjustment, including bereavement outcomes when appropriate, using a within and across group design (pre- and posttest design).

OUTLINE:

Patients and co-parents participate in the Enhancing Connections program consisting of 5 sessions over 1 hour each in the clinic or over the telephone. Session topics include managing cancer-related emotions when talking to children, developing deep listening skills, initiating difficult cancer-related conversations with children, interpreting a child's behavior, recognizing newly acquired gains from the program, and identifying available resources that can be used after program completion.

After completion of the study, participants are followed-up at 6 months.

Enrollment

15 patients

Sex

All

Ages

5 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

PATIENTS

Ages 25-65 years
Have a diagnosis of incurable cancer of any type; at any time in the diagnosis as long as they have at least a 4 month life expectancy based on the opinion of the attending physician
Read and write English among their languages of choice
Parent must live at least 50% of the time in the home and have a child 5-17 years old living at home who has been told their parent's cancer diagnosis

CO-PARENTS

Co-parents must reside with the consenting eligible cancer participant (and child) at least 50% of the time and be actively participating in the care of the child
If a biological parent lives in the home, and is physically well themselves, this person must be the co-parent
If a biological parent does not live in the home (or has died), the co-parent does not have to be a biological parent; therefore, co-parents may be step-parents, lesbian, gay, bi-sexual or transgender (LGBT) partners, grandparents, aunts, uncles, etc if they otherwise meet eligibility criteria
He or she can read and write English among their languages of choice and agrees to attend the patient intervention sessions in person or by telephone

CHILDREN

The patient and co-parent must agree to focus on the same child throughout the study and consent to have the child participate before the child's assent will be sought
Children aged 5-13 years of age will participate with a waiver of assent
Children aged 14-17 will assent to participate in the research study by signing a separate assent form
Children of formal assenting age will be eligible to participate if they can read and write English among their languages of choice

ALL PARTICIPANTS

Participants must live within 35 miles of the University of Washington, Seattle, WA to receive the in-person version of the intervention
Parents and co-parents selecting the telephone version of the intervention may live any distance from the University of Washington

Exclusion criteria

Patients will be excluded if they are enrolled in hospice at time of enrollment; however, they will be allowed to continue in the study if they enroll in hospice after beginning the study
The triad will be ineligible if any member lives in the home less than 50% of the time
If any member of the triad retracts consent or assent prior to completion of the post-intervention surveys, then all members will be excluded from the study thereafter
The child will be excluded if he or she has learning challenges as assessed by the patient or co-parent; patients and co-parents will be instructed to consider any formal diagnoses of a learning disability of the presence of an Individual Education Plan (IEP) when making this assessment