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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01577290
Enrollment
91
Registered
2012-04-13
Start date
2012-03-31
Completion date
2014-03-31
Last updated
2016-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Insomnia

Keywords

Anxiety, Depression, Insomnia, Mindfulness, Internet

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.

Interventions

BEHAVIORALInternet-administered Mindfulness Training Program

A 10 week, internet-administered mindfulness training program, featuring no therapist-support. 10 minutes of training, twice per day.

Access to a discussion group with the possibility of sharing experiences, methods of relief, and the like.

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Beck Anxiety Inventory (BAI)24 hours21 item rating scale for anxiety symptoms.

Secondary

MeasureTime frameDescription
Change from baseline in Beck Depression Inventory (BDI)24 hours21 item rating scale for depression symptoms.
Change from baseline in Quality Of Life Inventory (QOLI)24 hoursThe QOLI assessment yields an overall score and a profile of problems and strengths in 16 areas of life such as love, work and play. The QOLI test is a measure of positive psychology and positive mental health.
Change from baseline in Insomnia Severity Index (ISI)24 hours7 item rating scale of insomnia symptoms.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026