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Testing a daily smartphone-delivered intervention in individuals with work stress

Testing an intervention directed at reducing unconscious perseverative cognition

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28067
Enrollment
120
Registered
2014-10-01
Start date
2014-11-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stress, work load

Interventions

Experimental condition: problem-solving techniques, worry postponement, mindfulness exercises •Dose: daily, 5 times a day (between 9 AM – 11 PM) •Duration: 4 weeks (29 days) •Mode of administration

Sponsors

Leiden University
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: Person is not currently employed, currently being treated for a psychological or psychiatric disorder, substance abuse, no current or recent reports of suicidal ideation, history or presence of severe psychological disorders

Design outcomes

Primary

MeasureTime frame
•Implicit Positive and Negative Affect as measured with Implicit Positive and Negative Affect Test, time-point: post-intervention (i.e., 4-weeks). •Implicit stress as measured with the Implicit Association Test, time-point: post-intervention.

Secondary

MeasureTime frame
•Implicit Positive and Negative Affect as measured with Implicit Positive and Negative Affect Test, time-point: 2-weeks. •Implicit stress as measured with the Implicit Association Test, time-point: 2-weeks. •Explicit positive and negative affect as measured with the four basic emotions, time-point: 2-weeks, post-intervention. •Five Facet Mindfulness Questionnaire score, time-point: 2-weeks, post-intervention. •Effort-Reward Imbalance score, time-point: post-intervention •Trait worry, as measured by Penn State Worry Questionnaire, time-point: 2-weeks, post-intervention. •Anxiety symptoms as measured by GAD-7, time-point: 2-weeks, post-intervention. •Depressive symptoms as measured by PHQ-9, time-point: 2-weeks, post-intervention.

Contacts

Public ContactA. Versluis

Wassenaarseweg 52

A.versluis@fsw.leidenuniv.nl071-527 6343

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)