Actively Recruiting

Phase Not Applicable
Age: 15Years - 29Years
All Genders
NCT07138040

Re-Engaging AYA Survivors in Cancer-Related Healthcare

Led by Children's Hospital of Philadelphia · Updated on 2026-02-18

530

Participants Needed

3

Research Sites

143 weeks

Total Duration

On this page

Sponsors

C

Children's Hospital of Philadelphia

Lead Sponsor

N

Nationwide Children's Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to test the efficacy (how well they work) of different digital interventions that deliver information to adolescent and young adult (AYA) survivors of childhood cancer to promote re-engagement in cancer-related long-term follow-up care (LTFU). The main aims are: * To test the efficacy of adaptive interventions (AIs) that begin with low touch intervention (LTI) as compared to written information (WI) on attending an appointment, and self-reported self-management among AYA. * To identify the most efficacious second-stage strategy for those who initially schedule/attend an appointment (maintenance vs. step-up) and for those who do not (step-up vs. step-up maximum). * To assess multilevel factors contributing to the effects of re-engaging AYA and how best to integrate AIs into practice. Throughout the duration of the study, participants will complete four surveys, receive a series of interventions, and may be asked to participate in an interview (post-intervention).

CONDITIONS

Official Title

Re-Engaging AYA Survivors in Cancer-Related Healthcare

Who Can Participate

Age: 15Years - 29Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 15 to 29 years
  • History of childhood cancer diagnosed before age 22
  • No cancer-related follow-up visit in at least 15 months or 3 months past recommended follow-up
  • U.S. resident
  • Previously attended a cancer-related appointment at Children's Hospital of Philadelphia, Nationwide Children's Hospital, or Penn
  • At least 2 years from end of treatment and 5 years from diagnosis
  • Proficient in English
  • For participants under 18, a caregiver must provide informed consent
Not Eligible

You will not qualify if you...

  • Cognitive impairment that limits participation
  • Received only surgery as treatment
  • Transferred to primary care
  • Currently living with cancer diagnosis (new, metastatic, recurrence, or relapse)
  • No documentation of treatment history
  • Does not meet the inclusion criteria

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Nationwide Children's Hospital

Columbus, Ohio, United States, 43205

Actively Recruiting

2

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

3

Penn Medicine

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

L

Lisa Schwartz, PhD

CONTACT

S

Sara King-Dowling, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

7

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