No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
15 – 29
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
530 (estimated)
Sponsor
Children's Hospital of Philadelphia · Other
Who this trial is looking for
This trial is looking for young adults aged 15-29 who survived childhood cancer. Participants will receive digital support to help them attend follow-up care appointments and share their experiences through surveys and possible interviews.
Are You a Good Fit for This Trial?
You may be able to join if
I am aged 15-29.
I was diagnosed with childhood cancer before age 22.
I have not had a follow-up visit related to my cancer in at least 15 months.
I live in the U.S.
I previously attended appointments at specific children's hospitals.
It has been at least 2 years since my cancer treatment ended.
I speak English well.
If I am under 18, I have a caregiver who can consent for me.
You may not be able to join if
I have a cognitive impairment that limits my participation.
I only received surgery for my treatment.
I have been transferred to primary care for my follow-up.
I am currently living with cancer.
I do not have documented treatment history.
I do not meet the inclusion criteria listed above.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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) a…
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).
Trial Locations
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Eligibility Criteria
Inclusion Criteria for AYA
1. 15-29 years old
2. History of a childhood cancer diagnosis, diagnosed prior to age 22
3. Has not had a cancer-related follow-up visit in at least 15 months (or is 3 months past recommended follow-up)
4. U.S. resident (not international patient)
5. Has previously attend…
Inclusion Criteria for AYA
1. 15-29 years old
2. History of a childhood cancer diagnosis, diagnosed prior to age 22
3. Has not had a cancer-related follow-up visit in at least 15 months (or is 3 months past recommended follow-up)
4. U.S. resident (not international patient)
5. Has previously attended a cancer-related appointment at Children's Hospital of Philadelphia, or Nationwide Children's Hospital or Penn
6. At least 2 years from end of treatment and 5 years from diagnosis
7. English proficient
8. For AYA under age 18, must have a caregiver to provide informed consent
Exclusion Criteria for AYA
1. Cognitive impairment limiting participation
2. Received surgery only treatment
3. Transferred to primary care
4. Currently living with cancer diagnosis (either new, metastatic, recurrence, or relapse)
5. Absence of documentation of treatment history
6. Absence of inclusion criteria above
Inclusion Criteria for Support Person of AYA
1. Primary caregiver or other support person (e.g. partner, sibling, other caregiver)
2. At least 18 years old
3. U.S. resident
4. English proficient
Exclusion Criteria for Support Person of AYA
1. No involvement in the AYA's healthcare
2. AYA Decline support person's participation
3. Absence of inclusion criteria above
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