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Effect Evaluation of the Work Rehabilitation Effort Best iLag

Effect Evaluation of the Work Rehabilitation Effort Best iLag

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02945397
Enrollment
168
Registered
2016-10-26
Start date
2015-01-31
Completion date
2019-04-01
Last updated
2019-10-01

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

Conditions

Burnout, Professional, Musculoskeletal Pain, Work Related Illnesses

Keywords

Return to work, Work rehabilitation, Sick-leave

Brief summary

The study compares the effect of a group-based activity with an individual work-out activity on work participation.

Detailed description

The study is an RCT comparing the effect of a group-based intervention with an individual work-out intervention on work participation. The target group is persons who are at risk of leaving the work force due to health issues, and people currently outside the work force. The interventions have a time-span of 3 months. Survey data will be collected at baseline, after three months (after intervention has ended), and after 15 months. Survey data include information on lifestyle, self-reported health, subjective health complaints and readiness for work. Register data on employment and welfare benefits will be collected from two years in advance of inclusion, and five years after inclusion. According to power calculations, the study will need 322 participants. In addition to the effect evaluation, a process evaluation will also be performed. The process evaluation will examine content quality and adherence to guidelines, as well as feasibility of the group intervention. The process evaluation will consist of some survey data as well as interviews with service providers and participants.

Interventions

BEHAVIORALGroup-based activity

Regular follow-up from welfare authority as well as a 3 month group activity with weekly gatherings, focusing on coping, goal-setting and relevant information regarding available public services.

BEHAVIORALIndividual activity

Regular follow-up from welfare authority as well as a 3 month membership card at a given gym.

Sponsors

Norwegian Labour and Welfare Administration Tromso
CollaboratorUNKNOWN
NORCE Norwegian Research Centre AS
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Desire to work * Understand Norwegian sufficiently to complete surveys

Exclusion criteria

* Not able to participate in the interventions due to personal or health-related constraints.

Design outcomes

Primary

MeasureTime frame
Number of days at work during follow-up period measured through data from the Norwegian Labour and Welfare Administration´s databases.7 years

Secondary

MeasureTime frameDescription
Fatigue measured through questionnaire data.15 monthsChalder fatigue questionnaire
Self-rated health measured through questionnaire data.15 monthsGlobal health question
Sleep measured through questionnaire data.15 monthsSleep (single items)
Alcohol use measured through questionnaire data.15 monthsThe Alcohol Use Disorders Identification Test
Quality of life measured through questionnaire data.15 monthsEQ-5D (Health-related quality of life + visual analogue scale)
Subjective health complaints measured through questionnaire data.15 monthsSubjective health complaints inventory
Bullying measured through questionnaire data.15 monthsBullying (single items)
Social support measured through questionnaire data.15 monthsNon-directive and Directive Support Survey
Coping measured through questionnaire data.15 monthsTheoretically Originated Measure of Cognitive Activation Theory of Stress
Work readiness measured through questionnaire data.15 monthsReadiness for Return to Work Scale.
Regular exercise measured through questionnaire data.15 monthsRegular exercise (single items)

Countries

Norway

Outcome results

None listed

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