Testing daily smartphone-delivered interventions in individuals with workstress
Recruiting
- Conditions
- Individuals who experience work stress, defined as an effort-reward imbalance ratio of >1
- Registration Number
- NL-OMON29391
- Lead Sponsor
- eiden University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 180
Inclusion Criteria
Dutch speaking individuals who are employed, are 18 years or older, have an effort-reward imbalance ratio of >.89, and who have sufficient knowledge of how to work with a smartphone.
Exclusion Criteria
Person is not currently employed, has a latex allergy, currently being treated for a psychological or psychiatric disorder, has or has had a cardiovascular disease, substance abuse, no current or recent reports of suicidal ideation, history or presence of severe psychological disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ambulatory measured heart rate variability, timepoint: post-intervention (i.e., 4-weeks)
- Secondary Outcome Measures
Name Time Method •Ambulatory measured heart rate variability, timepoint: 2-weeks.<br /><br>•Ambulatory measured heart rate, timepoint: 2-weeks, post-intervention.<br /><br>•Implicit Positive and Negative Affect as measured with Implicit Positive and Negative Affect Test, timepoint: 2-weeks, post-intervention.<br /><br>•Implicit stress as measured with the Implicit Association Test, timepoint: 2-weeks, post-intervention.<br /><br>•Explicit positive and negative affect as measured with the four basic emotions, timepoint: 2-weeks, post-intervention.<br /><br>•Five Facet Mindfulness Questionnaire score, timepoint: 2-weeks, post-intervention.<br /><br>•Effort-Reward Imbalance score, timepoint: post-intervention<br /><br>•Trait worry, as measured by Penn State Worry Questionnaire, timepoint: 2-weeks, post-intervention.<br /><br>•Anxiety symptoms as measured by GAD-7, timepoint: 2-weeks, post-intervention. <br /><br>•Depressive symptoms as measured by PHQ-9, timepoint: 2-weeks, post-intervention. <br>