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Clinical Trials/NCT02241070
NCT02241070
Completed
N/A

The Potential for Mindfulness-Based Intervention in Workplace Mental Health Promotion: Results of a Randomized Controlled Trial

Chung Shan Medical University1 site in 1 country144 target enrollmentJune 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Mental Health Wellness 1
Sponsor
Chung Shan Medical University
Enrollment
144
Locations
1
Primary Endpoint
psychological distress
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The aims of the study are to determine the effectiveness of Mindfulness-Based Interventionas a workplace health promotion program on psychological distress, prolonged fatigue, job strain (job control and job demand), and perceived stress and to explore the influences of personal characteristics (including gender, age, education, and occupation) on the outcomes of the intervention with time.

Detailed Description

This study was one component of the Taiwan Workplace Mental Health Promotion Scheme. The study adopted a study design of a randomized controlled trial. Two large-scale manufacturing factories were chosen for this study. All of the factories' 3270 full-time employees were requested to fill in a questionnaire comprising questions regarding mental health and job strain. Of these employees, 2849 individuals were willing to complete the questionnaire. A total of 431 employees (15.13%) were found to be in psychological distress with job strain. The screening procedure was carried out between June and July in 2011. A letter of invitation with an introduction to MBI was sent to these employees. Of these 431 employees, only 144 responded that they would be willing to take part voluntarily in the study. These 144 workers were allocated randomly into the intervention group (Group I, n=72) or the waiting-list control group (Group C, n=72). All the participants were measured five times with an interval of four weeks between measurements. These measurements were taken at pre-intervention (T1), at mid-intervention (T2), at the completion of intervention (T3), four weeks after intervention (T4), and eight weeks after intervention (T5). The data related with the effectiveness of the intervention were obtained between August and December in 2011.

Registry
clinicaltrials.gov
Start Date
June 2011
End Date
December 2011
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

GCRC

Chung Shan Medical University

Chung Shan Medical University

Eligibility Criteria

Inclusion Criteria

  • Healthy employees with psychological distress and job strain
  • Full-time paid workers

Exclusion Criteria

  • Age \< 18y or \> 65y
  • Part-time workers
  • The workers are not willing to take part in the study

Outcomes

Primary Outcomes

psychological distress

Time Frame: four months

Psychological distress was measured by the Chinese Health Questionnaire (CHQ-12), a well-validated instrument

Secondary Outcomes

  • prolonged fatigue(Four months)
  • job strain(four months)
  • perceived stress(four months)

Study Sites (1)

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