Mindfulness Training for Staff (MTS)

Sponsor
University Hospital of North Norway (Other)
Overall Status
Completed
CT.gov ID
NCT01082497
Collaborator
(none)
53
1
2
20
2.6

Study Details

Study Description

Brief Summary

The purpose of this study is to investigate whether a mindfulness based 8-week course for stress reduction, known as MBSR course, given to all staff at an inpatient psychiatric ward influences the level of stress and burnout and the psychosocial atmosphere at the ward.

The design is an intervention trial with repeated measures and control group.The focus is the interaction between unit and individuals.

All staff at both wards were invited to participate. The intervention consists of 8 weekly group meetings where the participants learn different ways of practicing mindfulness and do home practice between the meetings. The control intervention is 8 weekly workshops in affect-consciousness.

Data are collected through self-reporting questionnaires on mindfulness, work- and health-related topics at six different points. The patients at both wards answers one questionnaire about ward atmosphere at the same points.

Data wil be analyzed on SPSS statistic programme.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness training
Early Phase 1

Detailed Description

MBSR for staff in inpatient psychiatric units

The challenges for staff working at an inpatient unit for psychotic people are many, and still more where the patients also have addiction problems. The patients are seriously ill and in need of extensive support and treatment. It is needed for the staff to be continuously aware and present, stand all kind of situations and hold out (contain) a lot of critique and threatening from the patients. Often they are too exhausted to take care of themselves and their own stress. The risk for burnout is high. The purpose of this study is to investigate whether a mindfulness based 8-week course for stress reduction, known as MBSR course, given to all staff at an inpatient psychiatric ward influences the psychosocial atmosphere at the ward.

The design of the study is an intervention trial with repeated measures and control group. The intervention consists of 8 weekly group meetings where the participants learn different ways of practicing mindfulness; sitting, walking, yoga exercises,and body scan.They are asked to practice between the group-meetings and get a workbook and cds as support.

This is a prospective intervention study with control group and repeated measures over one year follow up. The focus is the interaction between unit and individuals.

To more closely study the specific effect of mindfulness practice the control group receive an active intervention which has similarities to mindfulness practice: workshops in affect - consciousness of same amount as the MBSR-course.

All staff at the research unit and the control unit were invited to participate, each group has a number of 25 - 30 individuals. Data are collected through self-reporting questionnaires at six different points. The patients answers one questionnaire at the same points.

The inventories chosen are:

Demographics Quality of life Subjective health complains Five Facets Mindfulness Questioner (Baer) Maslach Burnout Inventory Work satisfaction Total Work load - short form Ward-atmosphere scale (also for the patients) Sick leave and number of registered harm /injury- episodes will be taken on 3 -4 points.

Hopefully this study will show that when the staff practice mindfulness this will bring about a more relaxed and accepting atmosphere followed by lesser exhaustion and anxiety. Consequences should be that mindfulness practise becomes more ordinary in psychiatric hospital wards.

Study Design

Study Type:
Interventional
Actual Enrollment :
53 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Mindfulness Training and Developing the Ability of Empathy at an Inpatient Ward for Dual Diagnoses
Study Start Date :
May 1, 2009
Actual Primary Completion Date :
Jan 1, 2010
Actual Study Completion Date :
Jan 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mindfulness

Behavioral: Mindfulness training
A course in mindfulness based stress reduction with 8 weekly group meetings and home practice between the meetings. Each meetings last for 90 minutes. Participants get workbook and cds to support home practice.
Other Names:
  • MBSR
  • Active Comparator: Education

    8 - weekly workshops on affect consciousness for all staff

    Behavioral: Mindfulness training
    A course in mindfulness based stress reduction with 8 weekly group meetings and home practice between the meetings. Each meetings last for 90 minutes. Participants get workbook and cds to support home practice.
    Other Names:
  • MBSR
  • Outcome Measures

    Primary Outcome Measures

    1. The ability of mindfulness measured by the Five Facet Mindfulness Questionnaire [Three months before to one year follow up after the intervention]

      The questionnaire measure the ability to observe, describe and act with awareness,nonreactivity and non-judgemental awareness.

    Secondary Outcome Measures

    1. The amount of work stress and burnout measured with The Maslach Burnout Inventory [Three months before intervention to one year follow up after the intervention]

      The questionnaire measure the dimentions emotional exchaustion,depersonalization and persomal accomplishment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • all staff working at the ward 50 % or more, not attending to leave during the first year.
    Exclusion Criteria:
    • Staff working less than 50%, planned to leave before one year.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital of North-Norway Tromso Troms Norway 9291

    Sponsors and Collaborators

    • University Hospital of North Norway

    Investigators

    • Study Chair: Tordis Sorensen Hoifodt, dr med. phd, University Hospital of North Norway

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital of North Norway
    ClinicalTrials.gov Identifier:
    NCT01082497
    Other Study ID Numbers:
    • P REK NORD-134/2008
    First Posted:
    Mar 8, 2010
    Last Update Posted:
    Apr 12, 2012
    Last Verified:
    Apr 1, 2012

    Study Results

    No Results Posted as of Apr 12, 2012