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NCT03481426 Clinical Trial

The Effect of Workplace Interventions on the Treatment of Low-back Pain

Back Pain Clinical Trial

Official title:
Workplace Interventions Supporting Employees to Continue at Work: Participatory Actions Organized by OH Physiotherapist

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03481426
Other study ID # ESormunen
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2017
Est. completion date August 30, 2019

Study information
Verified date April 2021
Source Finnish Institute of Occupational Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study evaluates the effect of workplace interventions on work ability promotion among workers with back problems. The half of participant will receive Information, advice and guidance for back problems in addition to participatory workplace actions organized by Occupational Health Physiotherapist. The other half will receive only Information, advice and guidance without workplace intervention.

Description:

Musculoskeletal symptoms, especially back pain, account for the majority of days lost. In order to enhance the health and working careers of people with MSD, it is important that work can be arranged in such a way that they can remain in work life despite MSD.In the field of work ability promotion, various stakeholders; the worker, employer, professionals in occupational health services (OHS) interact to optimize actions and practices to prevent absences from work and promote remaining at work. This study aims to investigate participatory working practices and modles of co-operation among OHS and workplaces.

Recruitment information / eligibility
Status Completed
Enrollment 107
Est. completion date August 30, 2019
Est. primary completion date April 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Back pain for at least two weeks or frequently occuring periods within the past 12 months Exclusion Criteria: - Back problems with forcoming surcical operation

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Workplace intervention
The study contains normal services of occupational health. Both intervention groups are based on voluntary will, and the normal care and services are guaranteed. In the intervention group new working method which improve co-operation between occupational health services and workplaces.

Locations
Country Name City State
Finland Finnish Institute of Occupational Health Helsinki

Sponsors (1)
Lead Sponsor Collaborator
Finnish Institute of Occupational Health

Country where clinical trial is conducted

Finland, 

Outcome
Type Measure Description Time frame Safety issue
Primary work ability The present self estimated work ability versus the life time best (0-10) through study completion, up to 12 months
Secondary intensity of pack pain The present self estimated back pain, no pain - the worst pain through study completion, up to 12 months
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