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No Fun No Glory: lifestyle and loss of pleasure

No Fun No Glory: lifestyle and loss of pleasure - No Fun No Glory: lifestyle and loss of pleasure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON42043
Enrollment
132
Registered
2015-03-10
Start date
2015-03-16
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

anhedonia loss of pleasure

Interventions

The group of 60 individuals without anhedonia will serve as a control group only during the observation month of the diary study, in which no intervention takes place, and will not partake in the in

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Screening;- 18-24 years old - Fluent in Dutch;Intervention;Anhedonic group: - persistent (> 2 months) anhedonia - willing to perform a tandem skydive;Control group: - no anhedonia - willing to perform a tandem skydive

Exclusion criteria

Exclusion criteria: Intervention - Inability to keep an electronic diary three times a day - Current professional treatment for psychiatric problems - Current use of psychopharmaca - Epilepsy - Pregnancy - Conditions that make it impossible to be attached to the tandemmaster (loose prostheses) - Height of more than 2 meters - Weight of more than 95 kg - Inability to raise ones legs 90 degrees (needed for save landing after tandem skydive) - Significant visual or hearing impairments - Previous experience with skydiving, bungee jumping, or base jumping - Cardiovascular complaints/problems

Design outcomes

Primary

MeasureTime frame
The main study endpoint of the intervention study is the level of pleasure, as measured in the daily questionnaires. We will follow two approaches to evaluate the effectiveness of the intervention. First, we will examine each individual series of observations to assess individual response patterns in pleasure scores. Second, to explore group-level patterns of change, we will evaluate possible differences between intervention groups in daily-reported pleasure.

Secondary

MeasureTime frame
Intervention study: As a secondary endpoint we will explore possible differences between intervention groups in monthly-reported pleasure in different dimensions (i.e., motivational, anticipatory, and consummatory dimensions) and different domains (i.e., physical, sexual, social, aesthetic, and intellectual domains).In addition to the level of pleasure endpoints, the effects of the intervention will also be examined with regard to changes in blood and saliva levels of potential biomarkers. Blood samples are taken at six different time points and saliva samples are taken four times on the day of the skydive intervention. Other secondary parameters that could affect the effectiveness of the intervention are (epi)genetic factors, 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. Furthermore, the dairy study will provide ample opportunity to examine the relations between mental and physical health, substance intake (i.e. food, alcohol, coffee, drugs) and sleep quality. Survey: Apart from as a screening tool, data from the survey will also be used to elucidate the various faces of pleasure loss, how often and in which combinations they occur in the general population, and how they relate to other variables such as lifestyle factors, (mental) health problems, personality, self-efficacy, emotion recognition skills and social position.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)