Ignite Creation Date:
2024-05-06 @ 4:10 PM
Last Modification Date:
2024-10-26 @ 2:05 PM
Study NCT ID:
NCT04897165
Status:
COMPLETED
Last Update Posted:
2021-06-08
First Post:
2021-05-18
Brief Title:
Resilience Training for Work-related Stress in Employees and the Influence of the Lecture Format on Training Success
Sponsor:
ARCIM Institute Academic Research in Complementary and Integrative Medicine
Organization:
ARCIM Institute Academic Research in Complementary and Integrative Medicine
Study Overview
Official Title:
Resilience Training With Mobile Heart Rate Variability Biofeedback for Work-related Stress in White-collar Employees and the Influence of the Lecture Format Digital vs Live on Training Success
Status:
COMPLETED
Status Verified Date:
2021-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
A study to analyze the psychophysiological effects of a preventative 4-week resilience training with mobile heart rate variability biofeedback HRV-BfB in a workplace setting and the influence of the lecture format digital vs live on the training success
Detailed Description:
This was a three-arm non-randomized controlled trial to examine the effects of a preventative 4-week resilience training with mobile HRV-BfB on work-related stress in white-collar employees Participants were asked to exercise autonomously three times per day for five minutes with the mobile HRV-BfB device They additionally attended three lectures at the beginning of the first third and forth week The aim of the lectures was to mediate a theoretical knowledge and to prepare the participants for the autonomous training To examine the potential influence of the lecture format one group attended live lectures blended learning condition and one group received access to online lectures e-learning condition Results of studys outcome measures were compared with a waitlist control group Outcome measures were assessed at baseline T0 after the 4-week intervention T1 and at 4-week follow-up T2
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None