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Recruiting NCT07141407

NCT07141407 Telephone-Based Coaching Sessions (TAC) to Improve Advance Care Planning Participation in Advanced Cancer Patients and Their Support Person

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Clinical Trial Summary
NCT ID NCT07141407
Status Recruiting
Phase
Sponsor Fred Hutchinson Cancer Center
Condition Advanced Malignant Solid Neoplasm
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2026-04-08
Primary Completion 2026-10-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Supportive CareTelephone-Based InterventionSurvey Administration

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 80 participants in total. It began in 2026-04-08 with a primary completion date of 2026-10-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This clinical trial studies whether telephone-based coaching sessions, Talking About Cancer (TAC), work to improve engagement in advance care planning (ACP) in patients with cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and their support person. Participation in ACP, which includes having end of life (EOL) care conversations and completing advance directives (e.g., living will, health care proxy, do not resuscitate order), improves quality EOL care. Despite this, less than half of patients with advanced cancer have EOL care conversations or complete advance directives. TAC coaching sessions are delivered by a social worker over the phone. They are designed to help patients and their support person communicate about ACP, manage the distress these conversations can cause, and participate in the process of ACP with a clear action plan of having goals-of-care conversations and completing advance directives. This may be an effective way to improve ACP participation in advanced cancer patients and their support person.

Eligibility Criteria

Inclusion Criteria: * PATIENT: Current diagnosis of stage III or IV cancer * PATIENT: Able to provide informed consent * PATIENT: Fluent in English or Spanish * PATIENT: Have access to a telephone, computer, or mobile device * CAREGIVER (SUPPORT PERSON): Person patient indicates provides support * CAREGIVER (SUPPORT PERSON): English or Spanish speaking * CAREGIVER (SUPPORT PERSON): 18 years of age or older * CAREGIVER (SUPPORT PERSON): Able to provide informed consent Exclusion Criteria: * PATIENT: Too ill or weak to complete the interviews (as judged by the interviewer) * PATIENT: Receiving hospice at the time of enrollment * PATIENT: Younger than age 18

Contact & Investigator

Central Contact

Megan Shen, PhD

✉ mshen2@fredhutch.org

📞 206-667-4172

Principal Investigator

Megan Shen, PhD

PRINCIPAL INVESTIGATOR

Fred Hutch/University of Washington Cancer Consortium

Frequently Asked Questions

Who can join the NCT07141407 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Advanced Malignant Solid Neoplasm. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07141407 currently recruiting?

Yes, NCT07141407 is actively recruiting participants. Contact the research team at mshen2@fredhutch.org for enrollment information.

Where is the NCT07141407 trial being conducted?

This trial is being conducted at Everett, United States, Mount Vernon, United States, Seattle, United States.

Who is sponsoring the NCT07141407 clinical trial?

NCT07141407 is sponsored by Fred Hutchinson Cancer Center. The principal investigator is Megan Shen, PhD at Fred Hutch/University of Washington Cancer Consortium. The trial plans to enroll 80 participants.

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