Can a smartphone app boost resilience in teens after surgery?
NCT ID NCT06991673
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
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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
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2025
- Expected to finish
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Dec 2029
An estimate. End dates often move.
- Lead sponsor
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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
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12 to 99 years
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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.
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The places running it
3 sites. The list below names each one and where it is.
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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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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
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Michigan Medicine- Brighton Center for Specialty Care
Brighton, Michigan, 48116, United States
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Michigan Medicine- East Ann Arbor Ambulatory Surgery and Medical Procedures Center
Ann Arbor, Michigan, 48109, United States
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University of Michigan affiliated hospitals
Ann Arbor, Michigan, 48109, United States
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