Moodpep
BehavioralSee arm description
NCT Number: NCT07030244
Depressive symptoms are prevalent among college students and often remain untreated. E-health interventions may help overcome treatment barriers by offering accessible and flexible support. This study will evaluate the effects of Moodpep, a guided online intervention for college students with depressive symptoms, and will examine predictors of treatment success and adherence.
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Notify Me16 year and older
All sexes
Interventional
Not applicable
VU Amsterdam, Amsterdam, Netherlands
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Eligible for Moodpep were students from the participating universities and universities of applied sciences: VU Amsterdam, Leiden University, Maastricht University, Utrecht University, Erasmus University Rotterdam, University of Amsterdam, InHolland University of Applied Sciences, Avans University of Applied Sciences and Rotterdam University of Applied Sciences.
The following inclusion criteria for Moodpep were used:
This last criterion was removed on May 9, 2023. After data collection, for statistical and content-related reasons, PhD students were removed from the analysis, just as students below 18 and above 30 years old, students who indicated their gender was other and students who completed less than 1 module of the intervention. This was done because the focus of the study was on students and not PhD students who are employees in the Netherlands, most students are between 18 and 30 years old, not enough students of another gender participated to include them separately in the analyses, and we were interested in the effects of Moodpep for students who started the intervention.
See arm description
Time frame: T0 (baseline), T1 (6 weeks post-baseline), T2 (6 months post-baseline)
Patient Health Questionnaire-9 (PHQ-9; Kroenke et al., 2001). Total scores range from 0 to 27 with higher scores indicating more depressive symptoms.
Time frame: T1 (6 weeks post-baseline)
Number of modules completed (1-8). For the logistic regression analysis, 2 categories will be made: participants who completed 1 module and participants who completed 2-8 modules.
Time frame: T0 (baseline)
Age, gender (male, female), nationality (Dutch, international), current psychotropic medication use (yes, no), and current psychotherapy (yes, no).
Universiteit Leiden
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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