Actively Recruiting
Optimizing ASCENT: A Digital Intervention Trial for Depression in Adolescent and Young Adult Cancer Survivors
Led by East Carolina University · Updated on 2026-01-07
208
Participants Needed
2
Research Sites
12 weeks
Total Duration
On this page
Sponsors
E
East Carolina University
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating a digital tool called the AYA Survivors Coping and Emotional Needs Toolkit (ASCENT) designed to help adolescent and young adult cancer survivors manage depression symptoms. This study aims to identify which parts or combinations of ASCENT's components contribute most to reducing depressive symptoms in young people who have completed cancer treatment. The study focuses on adolescents and young adults aged 15 to 39 who have finished cancer therapy within the past five years. Participants will be randomly assigned to one of sixteen conditions, each providing access to different combinations of ASCENT's components. All participants receive the core psychoeducation module about cancer survivorship and depression, plus daily mood tracking. Additional modules include positive psychology techniques, mindfulness training, cognitive restructuring, and behavioral activation. Each module contains micro-lessons with videos, stories, quizzes, open-ended questions, and practice activities, delivered digitally via smartphone. During the six-week intervention, participants complete mood tracking and engage with their assigned modules. Researchers measure changes in depressive symptoms from the start to week six, with a follow-up assessment at week twelve. Participants must have access to a smartphone and be fluent in English. Safety is monitored by excluding those with severe mental illness or suicidal intent. The study is sponsored by East Carolina University and aims to optimize depression support for young cancer survivors.
CONDITIONS
Brief Title
Optimizing the AYA Survivors' Coping and Emotional Needs Toolkit
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age at enrollment between 15 and 39 years
- Age at cancer diagnosis between 12 and 39 years
- Completed cancer treatment between 1 month and 5 years ago
- Fluent in English (spoken and written)
- Own a smartphone with a data plan
You will not qualify if you...
- Current diagnosis of severe or persistent mental illness
- Severe suicidal ideation, including plan and intent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - 6 weeks
Participants receive access to the ASCENT digital depression self-management tool with psychoeducational content and various intervention modules depending on their assigned condition.
Weekly visits or check-ins for 6 weeks
Duration - 6 weeks
Participants are monitored for changes in depressive symptoms after the intervention period.
1 to 2 visits depending on assessment schedule
Trial Site Locations
Total: 2 locations
1
East Carolina University
Greenville, North Carolina, United States, 27858
Actively Recruiting
2
Wake Forest University
Winston-Salem, North Carolina, United States, 27109
Actively Recruiting
Research Team
A
AnneMarie Coffey, BS
L
Lane Williamson
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
FACTORIAL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
16
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