Healthy sample
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age: 18-29 years Enrolled in university or technical college Normal or corrected vision
Exclusion criteria
Exclusion criteria: Contraindication to exercise (captured by PAR-Q; Adams, 1999). >1x/week >30 min of exercise of at least moderate intensity at a time, regularly, in the past three months (captured by SIMPAQ; Schilling et al., 2018) A total of =150 min of moderate-intensity or =75 min of vigorous-intensity physical activity, on average, per week, in the past three months (captured by SIMPAQ; Schilling et al., 2018)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome is executive functions (inhibition: stop-signal-reaction task, working memory: n-back task, set-shifting: trail making test Part B). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are symptoms of depression, anxiety, and stress (Depression, Anxiety, Stress Scale DASS-21) and subjectively perceived quality of life (World Health Organization Quality of Life - BREF questionnaire on quality of life; WHOQOOL-BREF) at the time point post-intervention and at the time of catamnesis. A further secondary outcome is the difference in executive functions between groups at the time of catamnesis. Control variables will be demographic variables and preferred intervention (at pre-intervention), self-reported exercise (Simple Physical Activity Questionnaire; SIMPAQ) and physical fitness (Shuttle-Run-Test, SRT) (at pre, post, catamnesis) and change in affect (SAM-Mannekin) during the intervention (at three time-points: first session, seventh session, twelfth session). Attendance and average, minimum, and maximum heart rates during the intervention will be recorded at each intervention session. | — |
Countries
Germany
Contacts
Eberhard Karls-Universität Tübingen, Wirtschafts- und Sozialwissenschaftliche Fakultät, Institut für Sportwissenschaft