Ignite Creation Date:
2024-10-26 @ 3:41 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06613529
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-08-29
Brief Title:
Effectiveness of Online Mindfulness Platform in Improving Anxiety Depression and Stress in Adult
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Effectiveness of Online Mindfulness Platform in Improving Anxiety Depression and Stress in Adults During the COVID-19 Pandemic a Randomized Control Trial
Status:
COMPLETED
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
During the COVID-19 pandemic adults may experience emotional stress and impact To reduce the risk of cross-infection this study aims to use online mindfulness training to improve emotional well-being during the pandemic and assess their effectiveness
Detailed Description:
he COVID-19 pandemic had a detrimental global impact on the health of most populations It causes and also generates further damage to physiology and psychology Mindfulness is recognized as an effective method for improving the symptoms of physical and mental problems The purpose of this review will explore the efficacy of an online mindfulness intervention for individuals or groups that impacted symptoms of physiology and psychology in adults during the pandemic base on the principle of evidence-based medicine At the same time a set of mindfulness intervention plans will be developed based on the best evidence searched and a pilot study will be conducted Therefore this research design will be divided into two stages In the first stage six electronic bibliographic databases will be comprehensively searched for randomized controlled trials that have been published from February 2020 to currently published articles The research subjects are adults who live in the community and accept online mindfulness intervention Quality assessment will be performed according to the Cochrane Collaborations Risk of Bias tool will be used for randomized controlled clinical trials RCTs A meta-analysis of the intervention timing and measurements will be performed using Review Manager 51 software The second phase will be a randomized controlled trial pilot study of mindfulness interventions The research subjects will be divided into two groups namely the mindfulness intervention experimental group E and the control group C The researcher uses structured questionnaires to collect data before intervention To and at 4 weeks T1 8 weeks T2 after the intervention Data will be analyzed using the Generalized Estimating Equation to analyze the repeated measurements and intention-to-treat analysis for reducing attrition bias
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None