MedPath

o Fun No Glory

Completed
Conditions
anhedonie
verlies van plezier
loss of pleasure
anhedonia
Registration Number
NL-OMON25879
Lead Sponsor
niversity Medical Center Groningen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

* Age 18-24 years

* Fluent in Dutch

Exclusion Criteria

* Inability to keep an electronic diary three times a day

* Current professional treatment for psychiatric problems

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The main study endpoint of the intervention study is the level of pleasure, as measured in the daily questionnaires. Change in pleasure will be evaluated both intraindividually (time series approach) and interindividually (multilevel approach).
Secondary Outcome Measures
NameTimeMethod
Secondary endpoints concern possible intervention effects in monthly-reported pleasure in different dimensions (motivational, anticipatory, consummatory) and different domains (perceptual, physical, social). Other endpoints that will be explored are changes in potential biomarkers, perceived physical and mental health, and positive and negative affect. Furthermore, the extent to which the lifestyle advice will lead to actual lifestyle change will be investigated by comparing the level and slope of the lifestyle variables in the pre- and post-intervention period.
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