Viewing Study NCT06420193


Ignite Creation Date: 2025-12-25 @ 12:59 AM
Ignite Modification Date: 2026-01-05 @ 1:48 AM
Study NCT ID: NCT06420193
Status: COMPLETED
Last Update Posted: 2025-07-10
First Post: 2024-05-07
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Evaluating Procedures for a Study of the AYA Survivors Coping and Emotional Needs Toolkit
Sponsor: East Carolina University
Organization:

Study Overview

Official Title: Evaluating the Feasibility and Acceptability of Study Procedures for a Full Factorial Trial of the AYA Survivors Coping and Emotional Needs Toolkit (ASCENT)
Status: COMPLETED
Status Verified Date: 2025-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ASCENT
Brief Summary: The investigators developed a digital intervention that aims to help adolescent and young adult cancer survivors (AYAs) manage symptoms of depression. This tool includes daily mood tracking, a psychoeducational module about cancer and depression, four components that are based on evidence-based interventions for depression. The goal of this study is to evaluate the acceptability of procedures for a future trial in which the investigators will test which component or combination of components meaningfully contribute to improvements in depressive symptoms among AYAs. Additionally, the investigators will evaluate study feasibility as well as intervention acceptability, satisfaction, usability, and engagement.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
R00CA248701 NIH None https://reporter.nih.gov/quic… View