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New app aims to empower young cancer survivors

NCT ID NCT07541183

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests a web app called MyCare eQuoL that helps childhood cancer survivors assess their needs and get personalized support. About 200 survivors aged 16-30 from nine European countries will use the app for six months. The goal is to see if the app helps them feel more in control of their health and improves their quality of life.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
MyCare eQuoL web app
What this could lead to
If it works, this could provide a practical tool to help childhood cancer survivors better manage their long-term care and communicate with doctors.
What could go wrong
This is an early-stage study with only 200 participants, so results may not apply to everyone. The app's benefits depend on user engagement and digital literacy.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Jun 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Childhood cancer survivors

Ages

16 to 30 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: \- Patients (male or female) with a history of cancer diagnosis before the age of 25 years * Patients aged between 16 and 30 years old as the study aims to primarily target digital natives who are familiar with mobile applications. * To be in follow-up care, completed follow-up, or lost to follow-up before inclusion at one of the institutions participating in the effectiveness study * Completed the planned treatment protocol * Without evidence of active disease and having been off therapy for at least 5 years since the first tumor diagnosis * Able to login and navigate phone apps * Sufficient language skills in one of the available study languages * With a valid informed consent from the patient, or, for patients younger than 18, valid consent from their parent/guardian and valid assent from the patient. Exclusion Criteria: Being unable to answer the questions of the study questionnaires (not even with help from another person) because of severe mental sequelae or insufficient mastery of the language used; ● currently in treatment for secondary malignancy or relapse of primary malignancy.-

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

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