Tokyo, May 2 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061405) titled 'A Study on Factors That Inhibit Well-Being in Workplace Environments' on May 1.

Study Type: Interventional

Study Design: Basic Design - Single arm Randomization - Non-randomized Blinding - Open -no one is blinded Control - Uncontrolled

Primary Sponsor: Institute - National Institute of Advanced Industrial Science and Technology (AIST)

Condition: Condition - Not applicable Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - This research project focuses on social communication-such as workplace meetings and discussions-which serves as a primary context in which stressors arise in workplace environments. Through in-situ measurements conducted during everyday meetings as well as controlled experiments using simulated meeting settings, the project aims to develop technologies for alleviating workplace stressors, thereby reducing workers' stress and contributing to improvements in their Quality of Life (QoL) and overall well-being. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - This study does not involve any specific intervention requiring participants to engage in additional physical activities or tasks beyond their normal routines. Data are collected during regularly conducted workplace meetings. Similarly, simulated meeting sessions are designed to reflect everyday meeting settings, in which participants are provided with typical agendas and roles and are asked to demonstrate meetings as they would normally occur in daily life.

Eligibility: Age-lower limit - 18 years-old

Gender - Male and Female Key inclusion criteria - Participants classified as internal members must meet all of the following criteria: 1) Be employed at the research implementing institution 2) Be able to provide written informed consent to participate in the study of their own free will 3) Be between 18 and under 70 years of age at the time consent is obtained 4) Be familiar with operating a personal computer (PC)

Participants classified as external members must meet all of the following criteria: 1) Be able to provide written informed consent to participate in the study of their own free will 2) Be between 18 and under 70 years of age at the time consent is obtained 3) Have experience in theatrical performance (acting) 4) Be able to travel independently to the experimental site 5) Be familiar with operating a personal computer (PC) Key exclusion criteria - Not applicable Target Size - 1100

Recruitment Status: Recruitment status - Enrolling by invitation Date of protocol fixation - 2025 Year 12 Month 02 Day Date of IRB - 2026 Year 03 Month 06 Day Anticipated trial start date - 2026 Year 05 Month 18 Day Last follow-up date - 2030 Year 03 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070242

Disclaimer: Curated by HT Syndication.