Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Anxiety Disorder
  • Obsessive Compulsive Disorder
Type
Interventional
Phase
Not Applicable
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 8 years and 17 years
Gender
Both males and females

Description

Aim The aim of this study is to conduct a pragmatic evaluation of ICBT for children and adolescents with anxiety disorders and OCD within routine health care in a rural area. Research questions Is ICBT an acceptable method for the patient group? Is ICBT effective in a clinical setting? Is further tr...

Aim The aim of this study is to conduct a pragmatic evaluation of ICBT for children and adolescents with anxiety disorders and OCD within routine health care in a rural area. Research questions Is ICBT an acceptable method for the patient group? Is ICBT effective in a clinical setting? Is further treatment needed after ICBT? What are the long-term effects of ICBT? What predicts treatment outcome? How does ICBT work in a clincal setting? (time spent, negative effects etc)? Design This is a uncontrolled intervention study where included families and children will be recruited consecutively during two years from a routine care CAMHS unit. All participants will be offered ICBT and assessed pre- and post-treatment, and at three-month follow-up through clinician ratings and self-report measures. The primary outcome measure is clinician rated severity of principal disorder at three-month follow-up. Long-term results will be assessed through study of medical records two years after completed ICBT.

Tracking Information

NCT #
NCT02926365
Collaborators
Not Provided
Investigators
Principal Investigator: Eva Serlachius, Med Dr Karolinska Institutet