Ignite Creation Date:
2024-05-06 @ 1:21 AM
Last Modification Date:
2024-10-26 @ 11:03 AM
Study NCT ID:
NCT01796054
Status:
COMPLETED
Last Update Posted:
2022-05-11
First Post:
2013-02-15
Brief Title:
Stress Free Now a Mind-body Reduction Program for Nurses
Sponsor:
The Cleveland Clinic
Organization:
The Cleveland Clinic
Study Overview
Official Title:
Effectiveness of a Mind-body Stress Reduction Program for Nurses A Randomized Controlled Study
Status:
COMPLETED
Status Verified Date:
2022-05
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:
SFN-Nurses
Brief Summary:
Mindful meditation sessions have been associated with an improvement in mindfulness perceived stress psychological well-being anxiety hostility and depression Meditation has been associated with a decrease in autonomic sympathetic activity heart rate oxygen consumption and energy expenditure Randomized controlled trials of online mindfulness and relaxation programs have been studied in patients with conditions such as irritable bowel syndrome headache depression fibromyalgia and insomnia Nurses may benefit from such programs given levels of job stress This study will determine whether an online stress reduction program that incorporates meditation with and without concomitant group support reduces burnout among nurses including emotional exhaustion and depersonalization The proposed research study will utilize Stress Free Now an online stress reduction program developed by Cleveland Clinic Wellness Institute
Detailed Description:
This is a randomized controlled single-center research study of an online intervention with peer group support to reduce stress in nurses All participants will be assigned to the intervention or control groups by random number allocation The duration of the intervention is 6 weeks follow-up is at 6 and 24 weeks the duration of the study is 6 months 24 weeks Total individual participant time commitment will depend on particular intervention or control group assignment Both intervention and control groups will be requested to complete a set of questionnaires at weeks 0 6 and 24 The questionnaires will take an estimated 45 minutes to complete
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