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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01920230
Other study ID # 21000021201
Secondary ID
Status Active, not recruiting
Phase N/A
First received July 29, 2013
Last updated December 1, 2015
Start date March 2013
Est. completion date February 2016

Study information

Verified date December 2015
Source University of Jyvaskyla
Contact n/a
Is FDA regulated No
Health authority Finland: Ministry of Social Affairs and Health
Study type Interventional

Clinical Trial Summary

The aim of this study is to examine the effectiveness of intervention based on mindfulness and acceptance-commitment therapy (ACT) in the recovery from job burnout. The 8-week intervention is delivered using jointly face-to-face group meetings and web-based program. The study hypothesizes that the Muupu-program is more effective than the normal practices when promoting work well-being in Finland. The participants are recruited from Finland.


Description:

Mindfulness-ACT-based interventions aren't widely used in Finnish work health care a the moment. This study examines the possibility of using this kind of intervention for reducing job burnout and stress and also promoting well-being at work. Muupu-program is standardized and can be administered in varying settings. If intervention is effective, it can have an impact on Finnish practices when treating job burnout and work-related stress.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 200
Est. completion date February 2016
Est. primary completion date February 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 25 Years to 60 Years
Eligibility Inclusion Criteria:

- Currently working

- Daily internet connection available

- Belongs to the group of most exhausted workers in Finland (BBI cut-off is set on the top 25%)

Exclusion Criteria:

- No psychological or somatic conditions or other practical reasons that hinder the possibility to participate to the program

- Acute medicine changes

- Regular psychotherapy

- Not willing to inform employer and/or work health care of participation to the study

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Mindfulness-ACT-intervention
Half of the participants (n=109) is assigned to intervention group. The intervention is based on Mindfulness-program presented by Williams & Penman (2011) and on principles of acceptance-commitment therapy (ACT). It aims to increase mindfulness skills and psychological flexibility through different exercises that are developed for improving skills of being present, dealing with thoughts and feelings as well as support clarifying individual values and value-based actions. The basic principles are presented in weekly small group meetings. Participants are guided to deepen their experiences through exercises and information that is provided via specific web-site.
No intervention
Half of the participants (n=109) don't get any special treatment. However the present study explores what kind of support they have had during the program.

Locations

Country Name City State
Finland University of Jyväskylä, Department of Psychology Jyväskylä

Sponsors (2)

Lead Sponsor Collaborator
University of Jyvaskyla Finnish Social Insurance Institution

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Other Utrecht Work Engagement Scale (UWES) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline work engagement at 2, 6 and 12 months No
Other Working conditions questionnaires used in Finlad Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline working conditions at 2, 6 and 12 months Yes
Other Depression, Anxiety and Stress Questionnaire (DASS) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline depression, anxiety and sress at 2, 6 and 12 months No
Other Psychological Well-being (by Ryff) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline psychological well-being at 2, 6 and 12 months No
Other Life Situation Questionnaire (LSQ, by Pulkkinen) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline life situation at 2, 6 and 12 months No
Primary Bergen Burnout Indicator (BBI) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline burnout at 2, 6 and 12 months No
Primary Perceived Stress Scale (PSS) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline stress at 2, 6 and 12 months No
Secondary Five Facet Mindfulness Questionnaire (FFMQ) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline mindfulness at 2, 6 and 12 months No
Secondary Acceptance and Action Questionnaire (AAQ-II) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline psychological flexibility at 2, 6 and 12 months No
Secondary Automatic Thought Questionnaire (ATQ) Study has 4 time points when the same questionnaires are administered to assess possible changes in outcome measures. Change from baseline automatic thoughts at 2, 6 and 12 months No
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