NCT07606443

Brief Summary

This study will test a novel intervention to facilitate family-centered communication among Hispanic/Latino (H/L) young adult childhood cancer survivors (YA-CCS), their support persons, and their clinicians through collaboration between the clinic and a community-based organization.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
18

participants targeted

Target at below P25 for not_applicable

Timeline
24mo left

Started Jul 2026

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 11, 2026

Completed
15 days until next milestone

First Posted

Study publicly available on registry

May 26, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

July 1, 2026

Expected
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2028

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2028

Last Updated

May 26, 2026

Status Verified

May 1, 2026

Enrollment Period

2 years

First QC Date

May 11, 2026

Last Update Submit

May 18, 2026

Conditions

Keywords

cancerhispanicyoung adult

Outcome Measures

Primary Outcomes (4)

  • Proportion of invited young adult cancer survivor-support person dyads enrolled

    Feasibility assessed by the proportion of invited dyads who enroll in the study.

    From recruitment initiation through completion of study enrollment, up to 24 months

  • Proportion of enrolled young adult cancer survivors completing all intervention components

    Feasibility assessed by the proportion of enrolled young adult cancer survivor participants who complete all intervention components.

    From intervention initiation through intervention completion, up to 3 weeks

  • Mean Theoretical Framework of Acceptability questionnaire score

    Acceptability assessed using participant-reported Theoretical Framework of Acceptability (TFA) questionnaire scores. Scores range from 1-5, with higher scores indicating greater acceptability.

    Post-intervention, within 2 months after intervention completion

  • Mean Satisfaction With Visit Preparation questionnaire score

    Acceptability assessed using participant-reported Satisfaction With Visit Preparation questionnaire scores. Scores range from -10 to 10, with higher scores indicating greater satisfaction.

    Post-intervention, within 2 months after intervention completion

Study Arms (1)

Family-Centered Communication

EXPERIMENTAL

Young Adult Cancer Survivors (YA-CCS)-support person dyads receive a family-centered communication intervention delivered by a community health worker and coordinated around a standard-of-care survivorship clinic visit.

Behavioral: Family-Centered Communication Intervention

Interventions

A novel family-centered communication intervention designed to facilitate communication among Young Adult Cancer Survivors (YA-CCS), their chosen support person, and clinicians through collaboration between the clinic and a community-based organization. The intervention includes pre-visit and post-visit sessions delivered by a community health worker and timed around a standard-of-care survivorship clinic visit.

Family-Centered Communication

Eligibility Criteria

Age18 Years - 25 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Childhood cancer survivor previously treated with chemotherapy and/or radiation therapy
  • Currently age 18-25 years
  • Identifies as Hispanic/Latino
  • Currently ≥5 years post cancer diagnosis
  • Fluent in English or Spanish
  • Receives medical care at Stanford
  • Lives within Jacob's Heart service area (zip codes within Monterey, Santa Cruz, Santa Clara, San Benito Counties: https://www.jacobsheart.org/service-area)
  • Ability to understand and the willingness to provide written informed consent.

You may not qualify if:

  • \. Lack of proficiency in written and spoken English or Spanish

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University

Palo Alto, California, 94304, United States

Location

MeSH Terms

Conditions

Neoplasms

Study Officials

  • Stephanie Smith, MD, MPH

    Stanford University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Stephanie Smith, MD, MPH

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 11, 2026

First Posted

May 26, 2026

Study Start (Estimated)

July 1, 2026

Primary Completion (Estimated)

July 1, 2028

Study Completion (Estimated)

July 1, 2028

Last Updated

May 26, 2026

Record last verified: 2026-05

Locations