Optimizing the AYA Survivors' Coping and Emotional Needs Toolkit
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age15-39
SponsorEast Carolina University
About this trial
Our team has developed a digital intervention that aims to help adolescent and young adult cancer survivors (AYAs) manage symptoms of depression. This tool includes one psychoeducation component and four components that are based on evidence-based interventions for depression. The goal of this study is to test which component or combination of components meaningfully contribute to improvements in depressive symptoms among AYAs.
Eligibility criteria
Qualifiers
Age at enrollment (adolescents 15-17, emerging adults 18-25, young adults 26-39)
Age at diagnosis (adolescents 12-17, emerging adults 15-25, young adults 15-39)
Time since completion of treatment: 1 month to 5 years
Language: Fluent in English (spoken and written)
Disqualifiers
Mental Health: Current diagnosis of severe or persistent mental illness
Suicidality: Severe suicidal ideation (including plan and intent)
Trial design
Treatments tested in this trial
- AYA Survivors Coping and Emotional Needs Toolkit (ASCENT)
Treatment groups
208 Participants
are divided into 16 treatment groups16
Treatment groupsSee each treatment group below.
Sponsors and collaborators
East Carolina University
Lead sponsor
National Cancer Institute (NCI)
Collaborator
Wake Forest University Health Sciences
Collaborator
Source ClinicalTrials.gov