Clinical trial Recruiting at 2 sites Interventional Ages 15 to 25

Survivors Journey+: an online family program for teen and young adult brain tumor survivors

Official title: Online Problem-Solving Intervention for Brain Tumor Survivors: A Two-site, Two-arm Pilot Randomized Controlled Trial

Run by Children's Hospital Medical Center, Cincinnati · NCT07321353 · Data updated 2026-11-12

This project will test whether the Survivors Journey+ online program with weekly coaching helps teen and young adult pediatric brain tumor survivors (ages 15–25) and their caregivers manage everyday challenges better than an information-only website.

More Pediatric Brain Tumor trials

Quick facts

Study typeInterventional
Ages15 Years to 25 Years
SexAll
Enrollment72 (estimated)
SponsorChildren's Hospital Medical Center, Cincinnati
Academic / other
Drugs / interventionschemotherapy, radiation
Locations2 sites (Cincinnati, Ohio and 1 other locations)
StatusRecruiting
StartedAugust 1, 2025
Main results expectedSeptember 2027
Study endsSeptember 2028
Registry record updatedJanuary 7, 2026
Trial IDNCT07321353 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are English-speaking pediatric intracranial tumor survivors ages 15–25 who completed tumor-directed treatment more than 12 months ago, live with a parent or guardian, and can participate in online coaching.

Probably not a fit

Those unlikely to benefit include people treated less than 12 months ago, individuals with tuberous sclerosis or neurofibromatosis, significant psychiatric disorders or recent psychiatric hospitalization, those not living in the family home, or households where English is not the primary language.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot randomized controlled trial will enroll pediatric brain tumor survivors ages 15–25 who live with a parent or guardian and randomize family dyads to either the Survivors Journey+ (SJ+) online program with weekly coaching or an internet resource comparison (IRC). The SJ+ program is a developmentally tailored, family-centered digital intervention that teaches social problem-solving, emotion-regulation, and metacognitive skills for survivors while offering caregiver strategies to reduce depression and family impact. Outcomes include feasibility and acceptability benchmarks (enrollment, retention, satisfaction) and measures of survivor and caregiver wellbeing collected at baseline and about three months post-baseline. The protocol also includes refining usability and accessibility based on participant feedback.

Why it matters

Potential benefit: If successful, SJ+ could improve survivors' quality of life, problem-solving and emotion-regulation skills while reducing caregiver distress and family burden.

How similar studies have gone: Some prior interventions for cancer survivors or caregivers have shown promise, but family-centered, developmentally tailored online programs for pediatric brain tumor survivors are relatively novel and remain untested at scale.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* a diagnosis of a pediatric intracranial tumor
* tumor-directed treatment completed \> 12 months ago (treatment included: surgery, radiation, or chemotherapy)
* lives with parent/guardian(s)
* language: English must be the primary spoken language in the home

Exclusion Criteria:

* history of tuberous sclerosis or neurofibromatosis
* treatment \< 12 months ago and/or treatment did not include surgery, radiation, or chemotherapy
* history of psychiatric hospitalization
* resides outside of the family home
* history of autism, reactive attachment disorder, psychosis, or other psychiatric diagnoses/conditions associated with significant risk of harm to self or others per caregiver
* English is not the primary language spoken in the home

Where it's running

  • Cincinnati Children's Hospital Medical Center
    Cincinnati, Ohio, United States
    Recruiting
  • Nationwide Children's Hospital
    Columbus, Ohio, United States
    Recruiting

Study contacts

  • Principal investigator: Shari L Wade, PhD — Children's Hospital Medical Center, Cincinnati
  • Study coordinator: Shari L Wade, PhD
  • Email: shari.wade@cchmc.org
  • Phone: 513-636-3370

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.