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Can a phone app ease stress for childhood cancer survivors?

NCT ID NCT06053268

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jul 24, 2026 · Updated 3 times

Summary

This study looks at whether a daily mindfulness app called Headspace can help adults who survived childhood cancer cope with stress. Fifty survivors will use the app for 30 days and wear a wrist device to track stress signs. The main goal is to see if people find the app acceptable and easy to use, not yet to prove it reduces stress.

What this could mean

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

Active substance
Headspace mobile mindfulness app
What this could lead to
If it works, this could point toward a simple, low-cost way to help childhood cancer survivors manage stress and improve their health.
What could go wrong
This is a very small, early feasibility study with only 50 participants. It is not designed to prove the app reduces stress, only that people will use it and that data collection methods work.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

50 people

The number who actually took part.

Started

May 2024

Expected to finish

Sep 2026

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.

Ages

18 years and older

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: * Research participant is at least 18 years old at enrollment * Research participant is followed by St. Jude Children's Research Hospital (SJCRH) * Research participant has a diagnosis history of leukemia or lymphoma * Research participant takes part in the St. Jude Lifetime Cohort Study (SJLIFE) * Research participant has elevated psychological stress scores of 6 or greater on most recent SJLIFE questionnaire * Participant can speak and read English Exclusion Criteria: * Research participant currently engages in mindful stress-reduction practices \>2x per week (e.g., tai chi, meditation) * Research participant takes psychiatric medications or medications that impact cardiac functioning, beta-blockers, alpha-blockers * Research participant wears a pacemaker * Research participant has a diagnosis of a congenital heart disease * Research participant has no access to a smartphone * Research participant has elevated pain interference scores (T≥70)

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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.

Contacts and locations

Locations

  • St. Jude Children's Research Hospital

    Memphis, Tennessee, 38105, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.