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Completed

NCT Number: NCT01402258

Internet-administrated Treatment of Anxiety Symptoms for Young Adults

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.

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Key information

Conditions

Anxiety Disorders Behavior Behavioral Symptoms Depression Mental Disorders

Age range

16 year–25 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Behavioral Sciences and Learning, Linköping University

Linköping, Östergötland County, 58183, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Tailored Internet-administrated CBT-Treatment

Behavioral

This intervention contains 6-8 text-based self-help modules in which 4 modules are fixed (the first three and the last) and the rest are prescribed following the diagnostic telephone interview. These modules contain material on panic disorder, social phobia, stress management, assertiveness training, concentration, relaxation among other things.

Primary outcomes

  1. Beck Anxiety Inventory (BAI)- Change from baseline

    Time frame: Two 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 outcomes

  1. Quality of Life Inventory (QOLI)- Change from baseline

    Time frame: Two 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.

  2. Montgomery Åsberg Depression Rating Scale-Self Rated (MADRS-S)- Change from baseline

    Time frame: Two 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.

  3. Clinical Outcome in Routine Evaluation - Outcome Measure (CORE-OM)- Change from baseline

    Time frame: Two 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.

Sponsors and collaborators

Lead sponsor

Linkoeping University

Other Gov

Registry information

Official study title

Tailored Internet-administrated Treatment of Anxiety Symptoms for Young Adults

Acronym: NOVA-IV

Important dates

Study start
2011
Primary completion
2014
Study completion
2015
First posted
Jul 26, 2011
Registry last updated
Dec 14, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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