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Internet-administrated Treatment of Anxiety Symptoms for Young Adults

Not Applicable
Completed
Conditions
Anxiety Disorders
Depression
Interventions
Behavioral: Tailored Internet-administrated CBT-Treatment
Registration Number
NCT01402258
Lead Sponsor
Linkoeping University
Brief Summary

The purpose of this study is to determine whether tailored internet-administrated CBT is a feasible approach in the treatment of anxiety symptoms and comorbid anxiety and depressive symptoms in a clinical setting.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
15
Inclusion Criteria
  • Be between the ages of 16-25 years old
  • Have anxiety symptoms and/or anxiety syndrome
Exclusion Criteria
  • Suicide prone
  • Alcohol addiction
  • Ongoing psychological treatment

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Tailored Internet-delivered CBTTailored Internet-administrated CBT-TreatmentBehavioral: Tailored Internet-delivered CBT
Primary Outcome Measures
NameTimeMethod
Beck Anxiety Inventory (BAI)- Change from baselineTwo weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

Change from baseline in anxiety symptoms two weeks post treatment, at six months and at 12 months post treatment.

Secondary Outcome Measures
NameTimeMethod
Montgomery Åsberg Depression Rating Scale-Self Rated (MADRS-S)- Change from baselineTwo weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

Change from baseline in depressive symptoms two weeks post treatment, at six months and at 12 months post treatment.

Clinical Outcome in Routine Evaluation - Outcome Measure (CORE-OM)- Change from baselineTwo weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

Change from baseline in anxiety and depressive symptoms two weeks post treatment, at six months and at 12 months post treatment.

Quality of Life Inventory (QOLI)- Change from baselineTwo weeks pre treatment, two weeks post treatment, six months and 12 months post treatment

Change from baseline in quality of life statements two weeks post treatment, at six months and at 12 months post treatment.

Trial Locations

Locations (1)

Department of Behavioral Sciences and Learning, Linköping University

🇸🇪

Linköping, Östergötland, Sweden

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