Effect Evaluation of a Workplace Intervention Targeting Subjective Health Complaints (atWork)
Primary Purpose
Mental Disorders, Back Pain, Anxiety
Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
The new atWork intervention
The original atWork intervention
Sponsored by
About this trial
This is an interventional prevention trial for Mental Disorders focused on measuring Sick leave, Mental Health, Coping, Social Support, Subjective Health Complaints
Eligibility Criteria
Inclusion Criteria:
- Norwegian primary education unit.
- Participants must be employed in one of the Norwegian primary education units participating in the study.
- Participants must have sufficient Norwegian reading and writing skills.
Exclusion Criteria:
- The organization has received the atWork intervention at an earlier time.
- Participants are not employed in one of the participating organizations.
- Participants do not have sufficient Norwegian reading and writing skills.
Sites / Locations
- Torill Helene Tveito
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
The new atWork intervention
The original atWork intervention
Arm Description
The intervention group will receive the new atWork intervention, which include a management course and workplace courses for all employees targeting mental health complaints and musculoskeletal complaints.
The control group will receive the original atWork intervention, targeting musculoskeletal complaint, and peer support.
Outcomes
Primary Outcome Measures
Sick leave, unit level
Sick leave at unit level will be collected through registry data from the Norwegian Labour and Welfare administration (NAV). Thus, we will collect data from all employees in participating units (approximately 100 units), not only the employees responding to questionnaires.
Secondary Outcome Measures
Coping Expectancies; Theoretically Originated Measure of the Cognitive Activation Theory of Stress, TOMCATS
All employees will be asked to complete questionnaires, one before the intervention and at 12 months follow-up.
Health; self-rated health, Subjective Health Complaints Inventory, SHC, Hopkins Symptom Checklist, HSCL-10
Job Satisfaction; Global Job Satisfaction, GJO, Demand-Control-Support-Questionnaire, short Swedish version
Social Support; Non directive and Directive Support Survey, NDSS-16.
Full Information
NCT ID
NCT02396797
First Posted
February 25, 2015
Last Updated
May 9, 2018
Sponsor
NORCE Norwegian Research Centre AS
Collaborators
The Hospital of Vestfold
1. Study Identification
Unique Protocol Identification Number
NCT02396797
Brief Title
Effect Evaluation of a Workplace Intervention Targeting Subjective Health Complaints
Acronym
atWork
Official Title
Effect Evaluation of a Workplace Intervention Targeting Subjective Health Complaints on Sick Leave, Coping, Health, Job Satisfaction and Social Support
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
January 2015 (Actual)
Primary Completion Date
May 2018 (Actual)
Study Completion Date
May 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NORCE Norwegian Research Centre AS
Collaborators
The Hospital of Vestfold
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Mental disorders is one of the most frequent causes of long-term sick leave and disability pensions in Norway, and there is a need for a comprehensive, coordinated response from health and social sectors at the country level to address the burden of mental disorders. The aim of this project is to investigate if a workplace intervention with the aim to increase coping of common mental health complaints and social support can reduce sick leave and improve health.
Detailed Description
The atWork intervention was established in 2007 as a new stepped-care approach to musculoskeletal complaints. The intervention consisted of workplace information meetings about musculoskeletal complaint to all employees and peer support. The atWork intervention targeting musculoskeletal complaints reduced sick leave and improved health in a randomized controlled trial. The atWork intervention has now been further developed with the aim to increase effect on sick leave and health. The intervention is now extended to include information about mental health complaints, in addition to a management course. The major societal costs and the negative consequences common mental health complaints induce underline the importance of testing if atWork is an effective way of reducing these consequences.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mental Disorders, Back Pain, Anxiety, Depression
Keywords
Sick leave, Mental Health, Coping, Social Support, Subjective Health Complaints
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1011 (Actual)
8. Arms, Groups, and Interventions
Arm Title
The new atWork intervention
Arm Type
Experimental
Arm Description
The intervention group will receive the new atWork intervention, which include a management course and workplace courses for all employees targeting mental health complaints and musculoskeletal complaints.
Arm Title
The original atWork intervention
Arm Type
Active Comparator
Arm Description
The control group will receive the original atWork intervention, targeting musculoskeletal complaint, and peer support.
Intervention Type
Behavioral
Intervention Name(s)
The new atWork intervention
Intervention Description
atWork is a cognitive intervention, and uses a nondirective delivery approach. It does not prescribe any change in lifestyle, but aims at establishing an understanding of common complaints and what to do when pain and health complaints occur. All information is based on the non-injury model, where pain and complaints are not signs of injury caused by wrongdoing or "inappropriate" behavior. The consistent take home message from all parts of the intervention is that keeping up usual activities, including going to work, is beneficial for health and recovery. This group will receive one management course, two workplace courses for all employees targeting mild mental disorders and nonspecific musculoskeletal complaints, and one reflection and review meeting.
Intervention Type
Behavioral
Intervention Name(s)
The original atWork intervention
Intervention Description
This group will receive three workplace courses for all employees targeting nonspecific musculoskeletal complaints, and peer support. Peer support involves selecting a peer advisor at the workplace. A peer advisor is a fellow worker without former medical training who as part of the atWork intervention receive more in-depth medical knowledge and training about nonspecific musculoskeletal complaints. The peer advisors role is to give social support and to use their local knowledge of the work place to facilitate staying at work for colleagues with health complaints.
Primary Outcome Measure Information:
Title
Sick leave, unit level
Description
Sick leave at unit level will be collected through registry data from the Norwegian Labour and Welfare administration (NAV). Thus, we will collect data from all employees in participating units (approximately 100 units), not only the employees responding to questionnaires.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Coping Expectancies; Theoretically Originated Measure of the Cognitive Activation Theory of Stress, TOMCATS
Description
All employees will be asked to complete questionnaires, one before the intervention and at 12 months follow-up.
Time Frame
1 year
Title
Health; self-rated health, Subjective Health Complaints Inventory, SHC, Hopkins Symptom Checklist, HSCL-10
Time Frame
1 year
Title
Job Satisfaction; Global Job Satisfaction, GJO, Demand-Control-Support-Questionnaire, short Swedish version
Time Frame
1 year
Title
Social Support; Non directive and Directive Support Survey, NDSS-16.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
67 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Norwegian primary education unit.
Participants must be employed in one of the Norwegian primary education units participating in the study.
Participants must have sufficient Norwegian reading and writing skills.
Exclusion Criteria:
The organization has received the atWork intervention at an earlier time.
Participants are not employed in one of the participating organizations.
Participants do not have sufficient Norwegian reading and writing skills.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Torill H Tveito, PhD
Organizational Affiliation
Uni Research Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Torill Helene Tveito
City
Bergen
Country
Norway
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
29785466
Citation
Johnsen TL, Eriksen HR, Baste V, Indahl A, Odeen M, Tveito TH. Effect of Reassuring Information About Musculoskeletal and Mental Health Complaints at the Workplace: A Cluster Randomized Trial of the atWork Intervention. J Occup Rehabil. 2019 Jun;29(2):274-285. doi: 10.1007/s10926-018-9786-6.
Results Reference
derived
PubMed Identifier
28820017
Citation
Johnsen TL, Eriksen HR, Indahl A, Tveito TH. Directive and nondirective social support in the workplace - is this social support distinction important for subjective health complaints, job satisfaction, and perception of job demands and job control? Scand J Public Health. 2018 May;46(3):358-367. doi: 10.1177/1403494817726617. Epub 2017 Aug 18.
Results Reference
derived
PubMed Identifier
27542921
Citation
Johnsen TL, Indahl A, Baste V, Eriksen HR, Tveito TH. Protocol for the atWork trial: a randomised controlled trial of a workplace intervention targeting subjective health complaints. BMC Public Health. 2016 Aug 19;16(1):844. doi: 10.1186/s12889-016-3515-x.
Results Reference
derived
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Effect Evaluation of a Workplace Intervention Targeting Subjective Health Complaints
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