Could Pixar's inside out help kids manage anxiety? a new study investigates
NCT ID NCT07708168
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This pilot study tests whether MyFILM, a 9-week group program using clips from the movie Inside Out, is feasible and acceptable for children aged 9-12 with mood or anxiety concerns. Participants attend weekly sessions to learn social-emotional skills and coping strategies. The study aims to gather preliminary data on whether the program improves emotional skills and reduces symptoms, preparing for a larger trial.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a 9-session group program called MyFILM that uses clips from the film Inside Out to teach social-emotional learning and coping skills
- What this could lead to
- If successful, this program could offer a new, engaging way to help children with mood or anxiety concerns build emotional skills and reduce symptoms.
- What could go wrong
- This is a small pilot study focused on feasibility, not proof of effectiveness. The results may not apply to all children, and the program may not lead to lasting improvements.
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 48 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2028
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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9 to 12 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: * Be between 9 and 12 years of age at enrollment * Be receiving outpatient care through Sunnybrook Health Sciences Centre * Demonstrate elevated risk (first-degree relative with a mental illness, experiencing a major life stressor as judged by the treating physician and investigator), subclinical symptoms (symptoms of a mood and/or anxiety disorder that do not meet the threshold of a clinical diagnosis), or diagnosed mood and/or anxiety-related concerns * Be able to participate in group-based discussions and activities in English * Have parent/guardian consent and participant assent Exclusion Criteria: * Have active psychosis or mania * Have severe cognitive, developmental, and/or behavioural limitations preventing meaningful participation
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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
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
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