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NCT07516353 · ClinicalTrials.gov registry record · NA

my.naviGATE: A Guide to After-Treatment Effects for Adolescents and Young Adults

A NA study, sponsored by Dana-Farber Cancer Institute.

Not yet
Registry status
NA
Development phase
143
Enrollment target

NCT07516353: Clinical Trial NA study, sponsored by Dana-Farber Cancer Institute.

NCT07516353 is a NA study that has not yet begun recruiting, run by Dana-Farber Cancer Institute. The registered enrollment target is 143 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07516353, a NA study, has not yet begun recruiting, sponsored by Dana-Farber Cancer Institute.

NOT YET RECRUITING
Registry status
NA
Development phase
143 participants
Enrollment target

Study Summary

This study aims to design and test a novel, personalized digital intervention-my.naviGATE-for adolescent and young adults (AYA) with cancer. my.naviGATE is a mobile app that provides personalized survivorship education, access to virtual peer navigation, and responsive participant-reported outcomes (PROs).

Primary Outcome

The Patient Activation Measure (PAM-13) is a validated, self-administered questionnaire assessing knowledge, skills, and confidence for self health-management. It has 13 items with a standardized score from 1-100 derived from 4-point Likert scale answer choices ranging from "Disagree Strongly" to "Agree Strongly;" a higher standardized score represents greater activation.

Interventions

  • BEHAVIORAL my.naviGATE Digital Tool

Trial Details

FieldValue
Enrollment Target 143 participants
Start Date 2026-08-20
Est. Completion 2030-12-31
Phase NA
Dana-Farber Cancer Institute

781 total trials

What is known before NCT07516353 opens enrollment

NCT07516353 is an interventional study that assigns participants to a tested intervention. The registered 143 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which my.naviGATE Digital Tool is the first listed.

NCT07516353 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07516353 about?

NCT07516353 is a clinical study titled "my.naviGATE: A Guide to After-Treatment Effects for Adolescents and Young Adults". This study aims to design and test a novel, personalized digital intervention-my.naviGATE-for adolescent and young adults (AYA) with cancer. my.naviGATE is a mobile app that provides personalized survivorship education, access to virtual peer navigation, and responsive participant-reported outcomes ...

What is the current status of trial NCT07516353?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 143 participants. The study started on 2026-08-20. Estimated completion is 2030-12-31.

What interventions are being tested in trial NCT07516353?

The interventions under investigation include: my.naviGATE Digital Tool (BEHAVIORAL).

Who is sponsoring clinical trial NCT07516353?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07516353's enrollment target sits among peer trials

143 711th of 2000 higher than 1,290 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07516353, the US trial registry maintained by the National Library of Medicine. NCT07516353 (mid enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.