Skip to main content
Clinical Trials/NCT01577290
NCT01577290CompletedNot Applicable

An Internet-administered, Mindfulness Training Program for the Treatment of Anxiety

Umeå University1 site in 1 country91 target enrollmentStarted: March 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
91
Locations
1
Primary Endpoint
Change from baseline in Beck Anxiety Inventory (BAI)

Study Overview

Brief Summary

The purpose of this study is to examine the effects of a 10 week mindfulness training program -- without therapist-support -- as treatment of anxiety. Effects on depression, quality of life, and insomnia symptoms will also be studied.

Detailed Description

Previous research has provided evidence for the thesis that training in mindfulness can decrease symptoms of anxiety and depression. This study will examine the effects of a 10 week mindfulness training program -- without therapist-support -- as treatment of anxiety. Effects on depression, quality of life, and insomnia symptoms will also be studied.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Satisfy DSM-IV criteria for an anxiety disorder
  • Living in Sweden and being able to read Swedish
  • Access to computer with internet connection

Exclusion Criteria

  • Currently receiving other psychological treatment
  • Non-stable use of psychoactive medication
  • Deemed suicidal
  • Deemed to suffer from other psychological disorder, e.g. psychosis, bipolarity etc.

Arms & Interventions

Mindfulness training

Experimental

Group receives mindfulness training.

Intervention: Internet-administered Mindfulness Training Program (Behavioral)

Discussion group

Active Comparator

Group has access to a discussion group.

Intervention: Discussion group (Behavioral)

Outcomes

Primary Outcomes

Change from baseline in Beck Anxiety Inventory (BAI)

Time Frame: 6 months

21 item rating scale for anxiety symptoms.

Change from baseline in Beck Anxiety Inventory (BAI)

Time Frame: 24 hours

21 item rating scale for anxiety symptoms.

Secondary Outcomes

  • Change from baseline in Beck Depression Inventory (BDI)(6 months)
  • Change from baseline in Quality Of Life Inventory (QOLI)(6 months)
  • Change from baseline in Insomnia Severity Index (ISI)(6 months)
  • Change from baseline in Beck Depression Inventory (BDI)(24 hours)
  • Change from baseline in Quality Of Life Inventory (QOLI)(24 hours)
  • Change from baseline in Insomnia Severity Index (ISI)(24 hours)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Per Carlbring, PhD

Professor

Umeå University

Study Sites (1)

Loading locations...

Similar Trials