Clinical trial · Interventional
Enhancing Connections Program in Improving Family Adjustment in Patients With Incurable Cancer
Family Functioning and Bereavement Outcomes Following the Enhancing Connections Program in Palliative Care
NCT03049397CI-TRIAL-00055073terminatedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Pilot deemed not feasible based on predetermined stopping rules
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Advanced Malignant Neoplasm | Malignant Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Communication Intervention | Other | — | UNRESOLVED |
| Questionnaire Administration | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Supportive Care (Enhancing Connections program)
- description
- 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.
- interventionNames
- Other: Communication Intervention
- Other: Questionnaire Administration
Primary outcomes (4)
- measure
- Feasibility of the Enhancing Connections program in advanced cancer patients and co-parents
- timeFrame
- Up to 2 years
- description
- Recruitment and retention of all triads will be monitored. Dosage and fidelity will be monitored for each intervention session. Program acceptability (per session, overall, duration of program, interval between intervention sessions) will be assessed from a debriefing interview. For logistics four areas will be monitored: rate of receipt of mailed materials both to participants and from participants; duration and type (whether telephone or in-person) of intervention sessions; rate of success in scheduling and completing intervention sessions with patient and co-parent; and quality of data on baseline, post-intervention and follow-up measures.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 5 Years
- Maximum age
- 65 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.