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Effectiveness of a Multi-Modal Workplace Rest Cabin on Worker Well-Being

NCT07322354 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 82

Last updated 2026-01-08

No results posted yet for this study

Summary

This study examines whether access to a rest cabin in the workplace supports employee well-being. Employees of a Canadian insurance company are randomly assigned to one of two groups: immediate access to the rest cabin or a waiting-list control group that receives access after one month. The rest cabin is installed directly in the workplace and can be reserved for short sessions during the workday. It offers multiple relaxation options, including guided meditation, massage therapy, light therapy, and a zero-gravity chair. Employees choose which options to use during each session. Participants complete questionnaires before group assignment and again one month later. Employees who receive immediate access to the cabin also complete additional follow-up questionnaires at later time points. The study compares changes in general well-being and work-related outcomes between employees who have access to the cabin and those who do not during the initial study period.

Conditions

  • Employee Well-being
  • Work-related Outcomes

Interventions

DEVICE

Recharjme Multi-Modal Rest Cabin

Enclosed workplace cabin with guided meditation, massage, luminotherapy, and zero-gravity chair.

Sponsors & Collaborators

  • Mitacs

    collaborator INDUSTRY

  • Laval University

    lead OTHER

Principal Investigators

  • Simon Coulombe, PhD · Laval University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-05-01
Primary Completion
2025-04-10
Completion
2025-04-10

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07322354 on ClinicalTrials.gov