Hair Cortisol and Symptoms in Children With Psychopathology During CBT

NCT ID: NCT06274424

Last Updated: 2024-02-29

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-01

Study Completion Date

2019-10-01

Brief Summary

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This study aims to examine the relationship between hair cortisol concentration and behavior and sleep disturbance symptoms in children with psychiatric disorders. It also investigates potential changes in hair cortisol and symptomatology after group-based cognitive behavior therapy. Furthermore, the study explores the effects of any alterations in hair cortisol concentration levels on potential behavior and sleep disturbance symptom change over the course of the study.

Detailed Description

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Conditions

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Child Behavior Problem

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Group Cognitive Behavioral Therapy Intervention

The Friends Program

Group Type EXPERIMENTAL

The Friends Program

Intervention Type BEHAVIORAL

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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* symptoms of anxiety or depression
* deficiencies in emotional and behavioral skills impairing functioning
* sufficient social and cognitive skills to participate in group work.

Exclusion Criteria

* excessive physical aggression
* excessive physical restlessness
* severity of psychiatric symptoms requiring individual psychotherapy (e.g., acute suicidality).
Minimum Eligible Age

6 Years

Maximum Eligible Age

13 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Helsinki University Central Hospital

OTHER

Sponsor Role lead

Responsible Party

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Sarianna Barron-Linnankoski

Principal Investigator

Responsibility Role 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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