- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01082497
Mindfulness Training for Staff (MTS) (MTS)
Mindfulness Training and Developing the Ability of Empathy at an Inpatient Ward for Dual Diagnoses
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.
Study Overview
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 Type
Enrollment (Actual)
Phase
- Early Phase 1
Contacts and Locations
Study Locations
-
-
Troms
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Tromso, Troms, Norway, 9291
- University Hospital of North-Norway
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mindfulness
|
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:
|
|
Active Comparator: Education
8 - weekly workshops on affect consciousness for all staff
|
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:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The ability of mindfulness measured by the Five Facet Mindfulness Questionnaire
Time Frame: 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.
|
Three months before to one year follow up after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The amount of work stress and burnout measured with The Maslach Burnout Inventory
Time Frame: Three months before intervention to one year follow up after the intervention
|
The questionnaire measure the dimentions emotional exchaustion,depersonalization and persomal accomplishment.
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Three months before intervention to one year follow up after the intervention
|
Collaborators and Investigators
Investigators
- Study Chair: Tordis Sorensen Hoifodt, dr med. phd, University Hospital of North Norway
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P REK NORD-134/2008
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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