Resilience Mobile App for Teens and Young Adults With Cancer

This study is testing a mobile app called mPRISM, which is a version of an existing program (PRISM) that teaches skills to help teens and young adults (ages 12-25) cope with stress, set goals, and use mindfulness during cancer treatment. The goal is to see if mPRISM is easy to use, helpful, and if it can improve your quality of life and reduce mental health symptoms like anxiety or depression. You may be able to join if you are 12-25 years old, have been diagnosed with a new cancer within the last year, are receiving chemotherapy or radiation at Seattle Children's Hospital, and can speak/read/write English or Spanish. This study is currently unclear on its recruitment status.

Study design
This is an interventional study planning to enroll 80 participants. It will use a waitlist control design, meaning some participants will receive the intervention right away, and others will receive it later.
What's involved
Participants will engage in a mobile health psychosocial intervention and interactive interviews. The exact number of visits or duration is not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary goals of the study, like how acceptable, appropriate, and feasible the intervention is, will be measured immediately after the intervention. Longer-term follow-up is not specified.

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NCT05842902

Resilience Mobile App for Teens and Young Adults With Cancer

Recruiting
NAAges 12–25InterventionalSupportive care
Seattle Children's Hospital
~80 participants
Updated 2026-08-03 on ClinicalTrials.gov
What's tested:mPRISM

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Acceptability of intervention
Measured over immediately post-intervention
+2 more outcomes measured
Cancer
1 sites across 1 states
Washington1

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Age 12-25 years
Diagnosis of new malignancy within 12 months of enrollment treated with chemotherapy and/or radiation therapy at Seattle Children's Hospital (SCH)
Patient able to speak/read/write English or Spanish language
Cognitively able to participate in mHealth psychosocial intervention and interactive interviews

Exclusion

Patient refusal to participate (any age), or parental refusal to participate for patients less than 18 years of age
Patients with diagnosis of malignancy \>12 months
Patients with relapsed, recurrent, or refractory disease
Patient without chemotherapy and/or radiation therapy as part of cancer treatment (e.g., surgical resection only patients are not-eligible)
Cognitively or physically unable to participate in mHealth psychosocial intervention and surveys
  • Acceptability of interventionimmediately post-intervention

    The Acceptability of Intervention Measure (AIM) is a well-validated 4-item scale that measures the perception among implementation stakeholders that a given treatment, service, practice, or innovation is agreeable, palatable, or satisfactory. Scale ranges from 4 to 20; higher scores are better.

  • Appropriateness of interventionimmediately post-intervention

    The Intervention Appropriateness Measure (IAM) is a well-validated 4-item scale that measures the perceived fit, relevance, or compatibility of the innovation or evidence-based practice for a given practice setting, provider, or consumer, and/or perceived fit of the innovation to address a particular issue or problem. Scale ranges from 4 to 20; higher scores are better.

  • Feasibility of interventionimmediately post-intervention

    The Feasibility of Intervention Measure (FIM) is a well-validated 4-item scale that measures the extent to which a new treatment, or an innovation, can be successfully used or carried out within a given agency or setting. Scale ranges from 4 to 20; higher scores are better.