Tailored Internet-delivered Cognitive Behaviour Therapy in Primary Care (TAYLOR2)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Gerhard Andersson, Linkoeping University
ClinicalTrials.gov Identifier:
NCT01591720
First received: April 18, 2012
Last updated: May 2, 2012
Last verified: May 2012
  Purpose

A tailored Internet-based cognitive-behavioural intervention is tested within a primary care clinic. Weekly measures of symptoms of depression and anxiety are obtained. Significant within-group effects are expected.


Condition Intervention
Depression
Anxiety Disorders
Behavioral: Tailored Internet-based CBT for depression and anxiety

Study Type: Interventional
Study Design: Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Effectiveness Testing of a Tailored Internet-delivered Cognitive Behaviour Therapy Treatment for Symptoms of Depression, Anxiety and Comorbid Problems

Resource links provided by NLM:


Further study details as provided by Linkoeping University:

Primary Outcome Measures:
  • Patient Health Questionnaire 9 (PHQ-9) [ Time Frame: 2 weeks before treatment starts ] [ Designated as safety issue: No ]
  • Patient Health Questionnaire 9 (PHQ-9) [ Time Frame: Weekly measures during treatment (for up to 16 weeks) ] [ Designated as safety issue: No ]
  • Patient Health Questionnaire 9 (PHQ-9) [ Time Frame: At treatment termination (after a maximum of 16 weeks) ] [ Designated as safety issue: No ]
  • Generalised Anxiety Disorder Assessment 7 (GAD-7) [ Time Frame: 2 weeks before treatment starts ] [ Designated as safety issue: No ]
  • Generalised Anxiety Disorder Assessment 7 (GAD-7) [ Time Frame: Weekly measures during treatment (for up to 16 weeks) ] [ Designated as safety issue: No ]
  • Generalised Anxiety Disorder Assessment 7 (GAD-7) [ Time Frame: At treatment termination (after a maximum of 16 weeks) ] [ Designated as safety issue: No ]

Enrollment: 64
Study Start Date: September 2010
Study Completion Date: August 2011
Primary Completion Date: August 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Tailored Internet-delivered CBT
The intervention is delivered within a primary care clinic.
Behavioral: Tailored Internet-based CBT for depression and anxiety
This Internet-based CBT intervention contains 8-10 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 interview. These modules contain material on panic disorder, social phobia, stress management, assertiveness training, concentration, relaxation among other things.

Detailed Description:

This Internet-based cognitive-behavioural therapy intervention contains 8-10 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 interview. These modules contain material on panic disorder, social phobia, stress management, assertiveness training, concentration, relaxation among other things.

The intervention is tested within a primary care clinic. Weekly measures of symptoms of depression and anxiety are obtained.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Symptoms of depression and anxiety

Exclusion Criteria:

  • Severe depression (based on interview)
  • Severe psychiatric condition (e.g. psychosis or bipolar disorder)
  • Suicidal (measured in diagnostic interview)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01591720

Locations
Sweden
Linköping University, Department of Behavioral Sciences and Learning
Linköping, Sweden, 58183
Sponsors and Collaborators
Linkoeping University
Investigators
Principal Investigator: Gerhard Andersson, PhD Department of Behavioral Sciences and Learning, Linköping University
  More Information

No publications provided

Responsible Party: Gerhard Andersson, Professor of Clinical Psychology, Linkoeping University
ClinicalTrials.gov Identifier: NCT01591720     History of Changes
Other Study ID Numbers: GA-VR-DEP-2
Study First Received: April 18, 2012
Last Updated: May 2, 2012
Health Authority: Sweden: The National Board of Health and Welfare

Additional relevant MeSH terms:
Anxiety Disorders
Depression
Depressive Disorder
Mental Disorders
Behavioral Symptoms
Mood Disorders

ClinicalTrials.gov processed this record on August 21, 2014