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Completed

NCT Number: NCT01347099

Internet-based Cognitive Behavior Therapy (CBT) for Obsessive Compulsive Disorder (OCD)

Cognitive behavior therapy (CBT) is an effective treatment for obsessive compulsive disorder (OCD) but there is a lack of properly trained CBT therapists. One possible treatment alternative is Internet-based CBT (ICBT) with minimal therapist input. The aim of this study was therefore to evaluate ICBT for OCD.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Psykiatri Sydväst

Stockholm, Sweden

About this study

This is a randomized controlled trial with 101 participants. The control group receives support therapy on demand on the Internet.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Primary diagnosis of obsessive compulsive disorder (OCD)
  • At least 18 years old
  • Able to read and write in swedish
  • Computer access

Exclusion criteria

  • other primary diagnosis
  • substance abuse,
  • psychosis,
  • bipolar disorder,
  • suicidal ideation,
  • adjusted pharmacological treatment the last two months
  • current psychological treatment for OCD,
  • been treated with CBT the last two years,
  • serious somatic disease,
  • Y---BOCS>31
  • hoarding as primary OCD subtype

Treatment and study plan

Internet-based Cognitive Behavior Therapy

Behavioral

Internet-delivered CBT. Contact with therapist thru an e-mail system. 10 weeks

Support therapy on Internet

Behavioral

Internet-delivered support therapy. Contact with therapist thru an e-mail system. 10 weeks

Primary outcomes

  1. Change from Baseline of obsessions and compulsions after 10 weeks and at 3- and 12 months after treatment.

    Time frame: Two weeks before treatment, 10 weeks after treatment starts, 3 and 12 months after treatment has ended

    Yale Brown Obsessive Compulsive Scale (Y-BOCS)

Secondary outcomes

  1. Change from Baseline of obsessions and compulsions after 10 weeks and at 3- and 12 months after treatment.

    Time frame: Two days before treatment, once per week for 10 weeks after treatment starts, 3 and 12 months after treatment has ended

    Obsessive Compulsive Scale - Revised (OCI-R)

  2. Change from Baseline of obsessions and compulsions after 10 weeks and at 3- and 12 months after treatment.

    Time frame: Two weeks before treatment, 10 weeks after treatment starts, 3 and 12 months after the treatment has ended

    Dimensional Obsessive Compulsive Scale (DOCS)

  3. Change from Baseline of depressive symptoms after 10 weeks and at 3- and 12 months after treatment.

    Time frame: Two weeks before treatment, 10 weeks after treatment starts, 3 and 12 months after treatment has ended

    Montgomery Asberg Depression Rating Scale

  4. Change from Baseline of meta cognitions after 10 weeks and at 3- and 12 months after treatment.

    Time frame: Two weeks before treatment, 10 weeks after treatment starts, 3 and 12 months after treatment has ended

    Obsessive Beliefs Scale

  5. Change from Baseline of quality of life after 10 weeks and at 3- and 12 months after treatment.

    Time frame: Two weeks before treatment, 10 weeks after treatment starts, 3 and 12 months after treatment has ended

    Euroqol

Sponsors and collaborators

Lead sponsor

Karolinska Institutet

Other

Registry information

Official study title

Internet-based Cognitive Behavior Therapy for Obsessive Compulsive Disorder: A Randomized Controlled Trial

Important dates

Study start
2011
Primary completion
2011
Study completion
2011
First posted
May 4, 2011
Registry last updated
Mar 21, 2018

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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