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Can a smartphone app boost resilience in teens after surgery?

NCT ID NCT06991673

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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jul 29, 2026 · Last updated Jul 30, 2026 · Updated 1 time

Summary

This study tests whether a mobile app called Ane-Roadmap can help adolescents aged 12 to 17 recover emotionally after a scheduled surgery. The app offers simple activities like savoring happy moments, keeping a gratitude diary, and planning pleasant events. Researchers want to see if teens and their caregivers will use the app regularly and find it helpful.

What this could mean

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

Active substance
a mobile app with resilience-building activities (Positive Piggy Bank, Gratitude Diary, Savoring, Pleasant Activity Scheduling)
What this could lead to
If the app is feasible and acceptable, it could provide a low-cost way to support emotional recovery after surgery in teens.
What could go wrong
This is a small feasibility study, not designed to measure health outcomes. The app may not improve recovery or be used consistently.

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

About 100 people

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

Started

Dec 2025

Expected to finish

Dec 2029

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

12 to 99 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 (Adolescent Patient): * Patient is aged 12-17 years on the date of surgery * Surgery is a scheduled surgery (non-emergency) * Surgery is occurring within the University of Michigan hospital system (University Hospital, C.S. Mott Children's Hospital, Brighton Ambulatory Surgery Center, East Ann Arbor Ambulatory Surgery Center) * Participants are able to enroll within 1-2 weeks of surgery * Patient and caregiver must be willing to participate * Adolescent and caregiver must have a compatible smartphone and/or tablet with internet access and be willing to download an app * Eligible patient is able to sign/assent form * Adolescent-caregiver dyad has at least one risk factor for adverse post-operative pain outcomes based on pre-enrollment screening (e.g., worries about managing pain, return to normal activities, limitations in doing desired activities, trouble with sleep) Inclusion Criteria (Caregiver): * Patient and caregiver must be willing to participate * Caregiver must be providing at least 50% of the patient's postsurgical caregiving * Caregivers agree to provide informed consent that is in regulatory compliance and IRBMED-approved and also in accordance with institutional guidelines * Adolescent and caregiver must have a compatible smartphone and/or tablet with internet access and be willing to download an app Exclusion Criteria (Adolescent Patient): * Adolescent or caregiver are unable to complete intervention activities or surveys in spoken or written English * Significant developmental delay, making it impossible for the participant to use an app to complete interventions or answer survey questions * Foster children or wards of the state are not eligible for inclusion * Hardware removal or debridement surgery (not considered as painful as other orthopedic surgeries) * Scoliosis surgery (due to extended longitudinal relationship with surgeon) * Concurrent participation in another behavioral/self-management intervention trial * Any impairment, activity, or situation that in the judgment of the Study Coordinator or Principal would make it inappropriate for the subject to participate Exclusion Criteria (Caregiver): * Significant developmental delay, making it impossible for the participant to use an app to complete interventions or answer survey questions * Adolescent or caregiver are unable to complete intervention activities or surveys in spoken or written English * Any impairment, activity, or situation that in the judgment of the Study Coordinator or Principal would make it inappropriate for the subject to participate

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As listed by the trial registrant

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

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    3 sites. The list below names each one and where it is.

  2. 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.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Michigan Medicine- Brighton Center for Specialty Care

    Brighton, Michigan, 48116, United States

  • Michigan Medicine- East Ann Arbor Ambulatory Surgery and Medical Procedures Center

    Ann Arbor, Michigan, 48109, United States

  • University of Michigan affiliated hospitals

    Ann Arbor, Michigan, 48109, United States

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