- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03634410
SeniorWorkingLife (Danish Title: SeniorArbejdsLiv) (SAL2018)
Study Overview
Status
Detailed Description
Due to demographic changes across Europe there are strong political interests in maintaining the labour force by prolonging working life, i.e. increasing retirement age. The present study investigates push and stay mechanisms for labor market attachment among older workers or people who have recently retired. The study is a questionnaire survey, which is already funded. The ambition is to apply for further funding to do a cohort that is repeated every 2-3 years, as well as long-term register follow-up in Danish national registers about health and work.
The study has 4 target groups:
- employed
- unemployed
- early retirement
- disability pension
The questionnaire survey is sent to 30,000 Danish citizens and contains the following 14 areas:
- Basic information (demographics, employment status etc.)
- Broad overview of factors that may influence labor market attachment (health, working conditions, economic factors)
- Role of the workplace
- Age-discrimination
- Economy
- Specific questions about the possibility for 'early retirement' among employed and unemployed
- Gradual retirement (e.g. possibility for reduced time or responsibility)
- Competencies and continuing education/training of skills
- Return-to-work
- New technologies at the workplace
- Job satisfaction and well-being
- Working environment (physical, psychosocial etc.)
- Lifestyle
- Health and functional capacity
The study is supported by a grant from TrygFonden
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Copenhagen, Denmark, 2100
- National Research Centre for the Working Environment
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
Labor market status of:
- employed (employed at least 20/37 hours per week 1.quarter of 2018) OR
- unemployed (unemployed at least 20/37 hours per week 1.quarter of 2018) OR
- early retirement OR
- disability pension
Exclusion Criteria:
- those that do not fullfill the above inclusion criteria
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
Employed
people aged +50 and currently employed
|
Unemployed
people aged +50 and currently unemployed
|
Early retirement
people aged +50 and currently on early retirement
|
Disability pension
people aged +50 and currently on disability pension
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Psychosocial Working Environment
Time Frame: Through study completion, an average of 2 year
|
Psychosocial Working Environment is measured using questionnaire
|
Through study completion, an average of 2 year
|
Physical Working Environment
Time Frame: Through study completion, an average of 2 year
|
Physical Working Environment is measured using questionnaire
|
Through study completion, an average of 2 year
|
Role of the workplace
Time Frame: Through study completion, an average of 2 year
|
Role of the workplace is measured using questionnaire
|
Through study completion, an average of 2 year
|
Age-discrimination
Time Frame: Through study completion, an average of 2 year
|
Age-discrimination is measured using questionnaire
|
Through study completion, an average of 2 year
|
Economy
Time Frame: Through study completion, an average of 2 year
|
Economic status is measured using questionnaire
|
Through study completion, an average of 2 year
|
Early retirement
Time Frame: Through study completion, an average of 2 year
|
Specific questions about the possibility for 'early retirement' among employed and unemployed
|
Through study completion, an average of 2 year
|
Gradual retirement
Time Frame: Through study completion, an average of 2 year
|
Gradual retirement (e.g.
possibility for reduced time or responsibility).
Questionnaire
|
Through study completion, an average of 2 year
|
Competencies
Time Frame: Through study completion, an average of 2 year
|
Competencies, education/training of skills will be evaluated using questionnaire
|
Through study completion, an average of 2 year
|
Return-to-work
Time Frame: Through study completion, an average of 2 year
|
Possibilities for returning to work for those currently not employed will be evaluated using questionnaire
|
Through study completion, an average of 2 year
|
New technologies
Time Frame: Through study completion, an average of 2 year
|
New technologies at the workplace will be evaluated using questionnaire
|
Through study completion, an average of 2 year
|
Job satisfaction
Time Frame: Through study completion, an average of 2 year
|
Job satisfaction will be evaluated using questionnaire
|
Through study completion, an average of 2 year
|
Sickness absence
Time Frame: Through study completion, an average of 2 year
|
Sickness absence will be evaluated through Danish registers
|
Through study completion, an average of 2 year
|
Disability pension
Time Frame: Through study completion, an average of 2 year
|
Disability pension will be evaluated through Danish registers
|
Through study completion, an average of 2 year
|
Mortality
Time Frame: Through study completion, an average of 5 year
|
Mortality will be evaluated through Danish registers
|
Through study completion, an average of 5 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Lifestyle
Time Frame: Through study completion, an average of 2 year
|
Lifestyle will be evaluated using questionnaire
|
Through study completion, an average of 2 year
|
Health
Time Frame: Through study completion, an average of 2 year
|
Health will be evaluated using questionnaire
|
Through study completion, an average of 2 year
|
Functional capacity
Time Frame: Through study completion, an average of 2 year
|
Functional capacity will be evaluated using questionnaire
|
Through study completion, an average of 2 year
|
Collaborators and Investigators
Publications and helpful links
General Publications
- Vinstrup J, Sundstrup E, Andersen LL. Psychosocial stress and musculoskeletal pain among senior workers from nine occupational groups: Cross-sectional findings from the SeniorWorkingLife study. BMJ Open. 2021 Mar 29;11(3):e043520. doi: 10.1136/bmjopen-2020-043520.
- Blafoss R, Skovlund SV, Lopez-Bueno R, Calatayud J, Sundstrup E, Andersen LL. Is hard physical work in the early working life associated with back pain later in life? A cross-sectional study among 5700 older workers. BMJ Open. 2020 Dec 7;10(12):e040158. doi: 10.1136/bmjopen-2020-040158.
- Skovlund SV, Blafoss R, Sundstrup E, Thomassen K, Andersen LL. Joint association of physical work demands and leg pain intensity for work limitations due to pain in senior workers: cross-sectional study. BMC Public Health. 2020 Nov 18;20(1):1741. doi: 10.1186/s12889-020-09860-6.
- Andersen LL, Sundstrup E. Study protocol for SeniorWorkingLife - push and stay mechanisms for labour market participation among older workers. BMC Public Health. 2019 Jan 31;19(1):133. doi: 10.1186/s12889-019-6461-6.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 70103
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Due to the requirements for anonymity of participants in research projects in Denmark, it has not yet been decided how to share the data.
People interested in performing analysis on the data should contact the research leader, Professor Lars L. Andersen, LLA@NRCWE.DK
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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