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Evaluating the Effectiveness of Multifaceted Implementation Strategies for Implementing a Guideline for the Prevention of Common Mental Disorders at the Workplace in Schools

Not Applicable
Completed
Conditions
Common Mental Disorders
Interventions
Behavioral: Single implementation strategy
Behavioral: Multifaceted implementation strategies
Registration Number
NCT03322839
Lead Sponsor
Karolinska Institutet
Brief Summary

Given today's high prevalence of common mental disorders and related sick leave among teachers an urgent need exists for a more sustainable working life for this professional group. One way of doing this is by improving schools' social and organizational risk management. Recent reports have shown that many schools in Sweden however lack a structured approach to the management of social and organizational risks. In 2015, we launched the first Swedish occupational health guideline to support a structured prevention of social and organizational risks at the workplace with the aim of preventing common mental disorders. The long-term goal of this study is to support the implementation of this guideline within schools in order to improve social and organizational risk management and in doing so reduce risk factors for mental ill-health and related sick days. The objective of the study is to fill the current research-to-practice gap by conducting a cluster-randomized controlled trial that compares the effectiveness of two implementation strategies for implementing the guideline in schools. The strategies that will be compared are training (ARM 1) versus training in combination with implementation teams and workshops (ARM 2). Our hypothesis for the study is that schools that receive support in implementing the guideline through combined strategies are more responsive to working in a structured and systematic manner with the management of social and organizational risks than schools that only receive training. The trial will be conducted in 20 primary schools in two municipalities in Sweden. All schools have agreed to participate. The primary outcomes are adherence to the guideline (implementation effectiveness) and self-reported exhaustion among schools personnel (intervention effectiveness); the secondary outcomes are risk factors for mental ill-health and absenteeism. Data will be collected at baseline, 6, 12 and 24 months by mixed methods (i.e. survey, focus-group interviews, observation, and register-data).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
732
Inclusion Criteria
  • all individuals who are employed by the participating schools
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Exclusion Criteria
  • individuals employed by the participating municipalities and not by the participating schools, for example cleaning personal. Individuals on sick-leave
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Single implementation strategySingle implementation strategyThe control-schools will only receive training to the school-management.
Multifaceted implementation strategiesMultifaceted implementation strategiesThe school-management will participate in a one-day training. In addition each intervention school will form an implementation team that is responsible for the implementation of the guideline within their school. The implementation teams will participate in 4-5 workshops in order to support the implementation process.
Primary Outcome Measures
NameTimeMethod
Exhaustion (intervention effectiveness)At baseline and 6, 12 and 24 months after baseline

Change from baseline in personnel's self-reported exhaustion during 6, 12 and 24 months follow. We hypothesize that adherence to the recommendations of the guideline will affect school personnel's self-reported exhaustion assessed with the Oldenburg Burnout Inventory (response format 1-4).

Guideline adherence (implementation effectiveness)At baseline and 6, 12 and 24 months after baseline

Change from baseline in adherence to the recommendations of the guideline during 6, 12 and 24 months follow-up period. We will use a questionnaire directed at the school management and a questionnaire directed at the school personnel. The questionnaires contain statements related to the recommendations in the guideline, such as "at our school we have clear and practical policies for preventing mental ill-health among our employees".

Secondary Outcome Measures
NameTimeMethod
Commitment to the workplaceAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported commitment as assessed by 3 items of the Copenhagen Psychosocial Questionnaire (response-form 1-5)

Social support superiorAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported social support from superior as assessed by 3 items of the Copenhagen Psychosocial Questionnaire (response-form 1-5)

RecoveryAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported recovery as assessed with 1 item (response-form 1-5)

Self-reported sickness absenteeismAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported sickness absenteeism as assessed by 2 items

BarriersAssessed during the 24 month study period

Information will be collected on possible barriers that may have influenced the implementation process. This data will be assessed by documentation.

Psychosocial safety climateAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported psychosocial safety climate as assessed by the 11-items of the Psychosocial Safety Climate Scale (response format 1-5)

Job demandsAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported job-demands as assessed by 11 items of the Copenhagen Psychosocial Questionnaire (response form 1-5)

Possibilities for developmentAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported possibilities for development as assessed by 4 items of the Copenhagen Psychosocial Questionnaire (response-form 1-5)

Work engagementAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported engagement as assessed by 3 items of the Utrecht Work Engagement Scale (response-form 1-7)

Work performance impairment due to problems in the work environmentAt baseline and 6, 12 and 24 months after baseline

Change from baseline in work performance as assessed by a question based on one item from the Work Productivity Activity Impairment - General Health Questionnaire (response format from 0-10)

Recognition (reward)At baseline and 6, 12 and 24 months after baseline

Change from baseline self-reported collaboration and leadership as assessed by 3-items of Copenhagen Psychosocial Questionnaire (response-format 1-5)

Influence at workAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported influence at work as assessed by 4 items of the Copenhagen Psychosocial Questionnaire (response-form 1-5)

Social support colleaguesAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported social support as assessed by 3 items of the Copenhagen Psychosocial Questionnaire (response-form 1-5)

Self-reported stressAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported stress as assessed with a single question (response-form 1-5)

Work-family conflictAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-reported work-family conflict as assessed with 4 items of the Copenhagen Psychosocial Questionnaire (response-form 1-4)

Work performance impairment due to health problemsAt baseline and 6, 12 and 24 months after baseline

Change from baseline in work performance as assessed by a question based on one item from the Work productivity Activity impairment - General Health Questionnaire (response format 0-10)

FacilitatorsAssessed during the 24 month study period

Information will be collected on possible facilitators that may have influenced the implementation process. This data will be assessed by documentation.

Self-perceived healthAt baseline and 6, 12 and 24 months after baseline

Change from baseline in self-perceived health as assessed with a single question (response-form 1-5)

Registered sickness absenteeism12 months prior to baseline, and during 24 months after baseline

Change in total sick-leave due to common mental disorders in days, register data (sickness benefit and disability pension).

Self-reported stress (SMS)Measured every 4th week over 12 months from baseline

Change from baseline in self-reported stress as assessed by one item sent by text-message by mobile-phone

Process evaluation dataAssessed during the 24 month study period.

Process data will be collected over the 24 months. This data will be assessed by documentation.

Trial Locations

Locations (1)

Unit for Intervention and Implementation Research for Worker Health, Institute for Environmental Medicine, Karolinska Institute

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Stockholm, Sweden

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