Smartphone app eases pain after scoliosis surgery in teens
NCT ID NCT04063670
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested whether giving teens extra education and coping skills through a smartphone app could help them manage pain and recover faster after scoliosis surgery. Forty adolescents aged 11 to 18 took part. The app provided videos on what to expect and how to cope, aiming to improve pain and function up to 6 weeks after surgery.
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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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40 people
The number who actually took part.
- Started
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May 2019
- Finished
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Aug 2021
- 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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11 to 18 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: \- All children ages 11 to 18 years old treated with primary multilevel spinal surgery of any approach Exclusion Criteria: * Non-English speaking * Non-idiopathic scoliosis, such as neuromuscular, congenital or syndromic. * Other comorbidity, including developmental delay. * Any surgical complication that results in significant divergence from our institution's standard scoliosis pathway. * Unplanned admission within 6 weeks of index operation. * Active treatment psychotherapy and/or cognitive behavioral therapy for any reason
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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
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University of California, San Francisco
San Francisco, California, 94158, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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