Tokyo, Dec. 31 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000060127) titled 'A Feasibility Study of a Mobile Application for Promoting Workplace Well-being Among Healthcare Professionals at St. Marianna University Hospital' on Dec. 31.

Study Type: Interventional

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

Primary Sponsor: Institute - St. Marianna University School of Medicine

Condition: Condition - healthcare professionals working at St. Marianna University Hospital Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - This study aims to preliminarily evaluate the feasibility of a mobile application, eMind for Business, customized for healthcare professionals at St. Marianna University Hospital, to promote mental health and well-being in the workplace. This study will assess the acceptability of the application (installation and usage rates) and its perceived usefulness (subjective evaluations and effects on work-related and psychological outcomes), to conduct an initial examination of its practicality and utility for implementation among healthcare professionals. Basic objectives2 - Others

Intervention: Interventions/Control_1 - Study participants will download the mobile application eMind for Business to their own smartphones. The application is designed to promote mental health and well-being in the workplace. During the intervention period, participants may use the following functions at their discretion: (1) a stress coping consultation function (AnyTalk) and (2) a health monitoring function (HeartPoint).

Eligibility: Age-lower limit - 20 years-old

Gender - Male and Female Key inclusion criteria - 1 Healthcare professionals working at St. Marianna University Hospital, including physicians, nurses/midwives, and pharmacists. 2 Individuals aged 20 years or older and under 75 years at the time of study enrollment. 3 Individuals who own a smartphone capable of installing the study application. 4 Individuals who are able to provide written informed consent to participate in the study. Key exclusion criteria - 1. Individuals for whom continued participation until the end of the intervention period is clearly difficult, such as those planning to resign or leave their position in the near future.

2. Individuals whom the investigators judge to be unsuitable for study participation due to health conditions or safety concerns. Target Size - 240

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2025 Year 11 Month 01 Day Anticipated trial start date - 2026 Year 01 Month 19 Day Last follow-up date - 2027 Year 03 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000068767

Disclaimer: Curated by HT Syndication.