Digital toolkit for helping young cancer survivors manage depression
Evaluating the Feasibility and Acceptability of Study Procedures for a Full Factorial Trial of the AYA Survivors Coping and Emotional Needs Toolkit (ASCENT)
This study is testing a digital tool to help young cancer survivors manage their depression and see how well they like and use it.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 16 (estimated) |
| Ages | 15 Years to 39 Years |
| Sex | All |
| Sponsor | East Carolina University Academic / other |
| Locations | 1 site (Greenville, North Carolina) |
| Trial ID | NCT06420193 on ClinicalTrials.gov |
What this trial studies
This study evaluates a digital intervention designed to assist adolescent and young adult cancer survivors in managing symptoms of depression. The intervention includes daily mood tracking and a psychoeducational module, along with evidence-based components aimed at improving mental health. The primary focus is to assess the acceptability and feasibility of the procedures for a future trial that will test the effectiveness of various components in alleviating depressive symptoms. Participants will provide feedback on their satisfaction, usability, and engagement with the toolkit.
Who should consider this trial
Good fit: Ideal candidates are adolescents and young adults aged 15-39 who have completed cancer treatment within the last 1 month to 5 years.
Not a fit: Patients with severe or persistent mental illness or those experiencing severe suicidal ideation may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the mental health and quality of life for young cancer survivors dealing with depression.
How similar studies have performed: Other studies have shown promise in using digital interventions for mental health support in cancer survivors, indicating a potential for success with this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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) * Technology: Own smart phone with data plan Exclusion Criteria: * Mental Health: Current diagnosis of severe or persistent mental illness * Suicidality: Severe suicidal ideation (including plan and intent)
Where this trial is running
Greenville, North Carolina
- East Carolina University — Greenville, North Carolina, United States (Recruiting)
Study contacts
- Principal investigator: Karly M Murphy, PhD — East Carolina University
- Study coordinator: AnneMarie Coffey
- Email: coffeya23@ecu.edu
- Phone: 252-328-6244
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.