Can your Child's doctor treat anxiety? a new approach puts it to the test
NCT ID NCT06104904
First seen Aug 12, 2026 · Last updated Aug 13, 2026 · Updated 1 time
Summary
This pilot trial tests whether pediatric primary care providers can effectively deliver a brief intervention called the Anxiety Action Plan (AxAP) to help children aged 6-17 with elevated anxiety symptoms. Providers receive training and coaching to administer the intervention, which is based on exposure therapy strategies. The study compares this approach to enhanced usual care, which includes educational videos and handouts. The goal is to see if this model is feasible and acceptable to providers and families, potentially improving access to anxiety care in community settings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Anxiety Action Plan (AxAP), a brief behavioral intervention based on exposure therapy, delivered by pediatric primary care providers
- What this could lead to
- If effective, this approach could expand access to anxiety care for children by equipping primary care providers to deliver brief, evidence-based interventions, especially in areas with few mental health specialists.
- What could go wrong
- This is a small pilot trial focused on feasibility, not proof of effectiveness. The intervention may not produce meaningful improvements in child anxiety outcomes, and results may not generalize to broader settings.
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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64 people
The number who actually took part.
- Started
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Nov 2023
- Finished
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Apr 2026
- 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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6 to 17 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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 for youth: * 6-17 years of age * Have elevated anxiety symptoms as indicated by a total Screen for Child Anxiety Rated Disorders score between 20 and 55 based on parent and/or child report Exclusion Criteria for youth: * Have a medical or psychiatric condition contraindicating participation (e.g., suicidality) based on clinical interview * Are receiving psychosocial mental health treatment for anxiety Inclusion Criteria for PCPs: * PCPs must have a PA, RN, NP, APRN or MD degree and be at least a part time employee in a primary care setting. There are no other inclusion/exclusion criteria.
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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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UConn Health
West Hartford, Connecticut, 06119, United States
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Other studies related to the condition(s) this trial covers.
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