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Trial of Health At Work Workplace Health Intervention

A Pilot Controlled Feasibility Trial of Early Health At Work Workplace Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00858533
Acronym
H@W
Enrollment
63
Registered
2009-03-10
Start date
2008-06-30
Completion date
2010-03-31
Last updated
2024-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Workplace Health

Keywords

early intervention, sickness absence, return to work, primary care

Brief summary

This pilot study will compare workplace health intervention delivered by advisors based in GP practices with normal GP care to assess the usefulness of the concept and its potential for wider use in a larger randomised controlled trial.

Detailed description

The aim of this pilot study is to examine the impact of H@W intervention(s) on job retention and return to work and compare outcomes with those from normal GP care. The target population for this study is people still at work but experiencing a work-related health problem as well as those off work. For the purpose of the study, short term sickness absence is defined as a period of 4 weeks or less and long term sickness absence defined as a period of 4 weeks or longer. Hypothesis That H@W intervention in comparison to standard care: * promotes work retention * enables a quick and sustained return to work for those on short term sick leave (4 weeks or less) * achieves sustained return to work for those on long term sick leave of 4 weeks or more. This could include a phased return to work. * achieves positive outcomes which could mean leaving one job and starting another.

Interventions

BEHAVIORALHealth at Work workplace health advice and support

The intervention group will receive additional support from a H@W Workplace Health Advisor who will deliver an intervention aimed at sickness absence prevention or sustained return to work, depending on individual circumstances. The intervention will be standardized as far as possible to show types of activity undertaken with participants, their GP, line managers, human resources departments and trade union representatives.

Sponsors

University of Liverpool
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* People with work related health problems registered with GP practices in Liverpool Primary Care Trust.

Exclusion criteria

* People registered with GP practices outside Liverpool Primary Care Trust. * Vulnerable adults and those considered by their GP to be unsuitable for the trial.

Design outcomes

Primary

MeasureTime frame
Number of days off work through sickness absence after index consultation, which will also apply to people at work with a work-relevant condition1 year

Secondary

MeasureTime frame
Secondary outcome measure: time to first return to work (RTW) allowing for phased return.1 year

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026