Could an 8-Day therapy course help teens overcome panic and agoraphobia?
NCT ID NCT00576719
First seen Jul 21, 2026 · Last updated Jul 22, 2026 · Updated 1 time
Summary
This study tests whether an intensive, 8-day form of cognitive behavioral therapy (CBT) can help adolescents with panic disorder and agoraphobia. The therapy includes 15-20 hours of one-on-one sessions focused on changing anxious thoughts and gradually facing feared situations. Some teens receive the therapy alone, while others have their parents involved. The goal is to see if this short but intense approach reduces panic attacks, fear, and avoidance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- intensive cognitive behavioral therapy (CBT) with exposure, delivered over 8 days with 15-20 hours of therapist contact
- What this could lead to
- If successful, this could provide a fast, effective treatment option for teens with panic disorder and agoraphobia, reducing symptoms and improving daily functioning.
- What could go wrong
- This is a small, early-stage study with 63 participants, so results may not apply to all teens. The intensive format may be hard to fit into regular care, and long-term benefits are not yet known.
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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63 people
The number who actually took part.
- Start date
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Mar 2005
- Finished
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Mar 2011
- 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 17 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: * Meets DSM-IV criteria for principal diagnosis of PD or PDA prior to treatment * Adolescent must be accompanied by at least one parent or caregiver * If on medication, there must be a 1-month stabilization period for benzodiazepines or 3-month stabilization period for SSRIs or tricyclics prior to study entry Exclusion Criteria: * Positive diagnosis of schizophrenia, pervasive developmental disorder, organic brain syndrome, mental retardation, or current suicidal ideation * Unavailability of at least one parent or caregiver * Refusal of parent to accept random assignment to treatment condition * Refusal of parent or adolescent to accept stabilization of medication * Adolescent with parent who has any condition that would limit ability to understand treatment
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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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Boston University
Boston, Massachusetts, 02215, United States
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Other studies related to the condition(s) this trial covers.
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