Vital@Work: Reintegration Program for Employees with Stress-related Complaints

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-68
SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

About this trial

The objective of this study, Vital@Work reintegration program, is to support sick-listed workers with stress-related complaints in their return to work based on a personalized program. Therefore, the aim of this study is test whether participants supported by a tailored eHealth program, and if needed, additionally supported by a structured and stepwise Participatory Approach (PA) involving the sick-listed worker, their direct supervisor and a neutral party, show a faster and sustainable return to work as compared to participants in the control condition. This program is investigated in four different organizations, which differ in sector, size (small and large organizations), type of organization (private or public) and type of work.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Sick-listed employees from participating organisations (Amsterdam UMC, GGZ inGeest, Rijksschoonmaakorganisatie [RSO], and Transavia)

Aged 18-68

Between 2 and 12 weeks on sick leave

Suffering from stress-related complaints

Disqualifiers

Non-sick-listed employees

Suffering from severe psychiatric disorders (e.g., suicidality, mania, psychosis, schizophrenia) or other chronic conditions (e.g., terminal illness) that could significantly affect the employee's mental health and, hence, prevent the return-to work process

Being pregnant or less than three months after delivery

Sick-listed for more than 12 weeks

Trial design

Design model

Parallel

Treatments tested in this trial

  • Return to work program

    Other intervention

    The eHealth modules focus on psychoeducation, perceptions of return to work based on a personal plan including problem-solving exercises, relapse prevention, and continuous monitoring. If needed, followed by the participatory approach, a stepwise, collaborative approach to analyse and solve bottlenecks to develop a consensus-based plan for return to work.

Treatment groups

208 Participants
are divided into 2 treatment groups
Group A: eHealth with Participatory Approach if neededExperimental treatment 1 intervention
Group B: Control conditionNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Lasting return to work

Lasting return to work of at least 28 consecutive days without (partial or full) relapse

Time frame
Baseline - 3 months - 6 months -12 months

Secondary outcomes

1

Stress-related complaints

Stress-related complaints (e.g., type of disease, severity of symptoms) by means of the 4DKL (Terluin, 2008), Promis (Terwee et al. 2015).

Time frame
Baseline - 3 months - 6 months -12 months
2

Psychosocial job characteristics

Psychosocial job characteristics (e.g., mental workload, decision latitude, social support, physical demands, job insecurity) by means of the JCQ (Karasek, Houtman et al. 1995)

Time frame
Baseline - 3 months - 6 months - 12 months
3

Behaviour change

Behaviour change (e.g., attitude, social influence, self-efficacy); by means of the ASE (Damoiseaux et al. 1998), RTW-SE (Volker et al. 2015).

Time frame
Baseline - 3 months - 6 months - 12 months

Other outcomes

Sponsors and contacts

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