Hair Cortisol and Symptoms in Children With Psychopathology During CBT
NCT ID: NCT06274424
Last Updated: 2024-02-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
100 participants
INTERVENTIONAL
2016-07-01
2019-10-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Group Cognitive Behavioral Therapy Intervention
The Friends Program
The Friends Program
A group CBT intervention comprising ten weekly 60-minute sessions followed by two booster sessions.
Interventions
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The Friends Program
A group CBT intervention comprising ten weekly 60-minute sessions followed by two booster sessions.
Eligibility Criteria
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Inclusion Criteria
* deficiencies in emotional and behavioral skills impairing functioning
* sufficient social and cognitive skills to participate in group work.
Exclusion Criteria
* excessive physical restlessness
* severity of psychiatric symptoms requiring individual psychotherapy (e.g., acute suicidality).
6 Years
13 Years
ALL
No
Sponsors
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Helsinki University Central Hospital
OTHER
Responsible Party
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Sarianna Barron-Linnankoski
Principal Investigator
Other Identifiers
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HUS/211/2016 and HUS/2699/2018
Identifier Type: -
Identifier Source: org_study_id
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