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VRelax at work

Virtual Reality relaxation for work-related stress - a multiple baseline intervention study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23543
Enrollment
50
Registered
2021-03-09
Start date
2021-03-10
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Burn-out

Interventions

Daily 20-minute use of self-management VR relaxation tool at home during three weeks.

Sponsors

University Medical Center Groningen, Groningen, the Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - >18 years of age. - Parttime or fulltime employed. - At least moderate level of self-reported psychosocial stress. - At least mild burn-out symptoms, judgement of occupational health service worker.

Exclusion criteria

Exclusion criteria: - IQ <70. - Poor vision. - Actual epilepsy (convulsion during past 12 months).

Design outcomes

Primary

MeasureTime frame
As the primary outcome data has a multilevel structure (multiple VAS session scores within participants), VAS scores are analyzed with mixed model multilevel regression analyses (MIXED command), including factor time (length of baseline and before vs. after session). Models have a random intercept for participant. The estimation method is set to restricted maximum likelihood and the covariance structure to unstructured. The immediate effects of VRelax is analyzed by comparing mean VAS scores between multiple baseline and intervention periods, and before and after sessions. Covariates include sociodemographic characteristics and baseline level of stress, symptoms and functioning.

Secondary

MeasureTime frame
Mean scores on the questionnaires will be compared between baseline and end of treatment, using repeated measures ANOVA. Use of medication and substances will be compared between baseline and end of treatment with repeated measures ANOVA. Other parameters used as covariates in analyses of primary and secondary outcomes.

Contacts

Public ContactBart Lestestuiver

UMCG

b.p.lestestuiver@umcg.nl0503615466

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)