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Effectiveness of Moodpep and SpiralUp! for student depression

Effectiveness of two guided internet-based self-help programs in reducing depressive symptoms in university students: Randomized controlled trial - Effectiveness of two guided internet-based interventions versus waitlist control on depressive symptoms in university students: an RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58537
Enrollment
429
Registered
2025-05-21
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Depressive symptoms, subthreshold depression, elevated depressive mood, mild to moderate depression, psychological distress Mood problems in students

Interventions

The interventions under investigation are two digital, cognitive behavioral therapy (CBT)-based programs delivered through the MoodLift platform, developed for university students. 1.&nbsp
&nbsp
Moodpep is a guided online self-help program that spans approximately 6 to 8 weeks. It includes core CBT components such as behavioral activation, cognitive restructuring, and relaxation techniques. P
SpiralUp! is a brief, single-session intervention also based on CBT principles, with a focus on behavioral activation and goal-setting. Participants receive one-time written feedback from a coach afte

Sponsors

Vrije Universiteit
Lead Sponsor

Eligibility

Age
16 Years to 64 Years

Inclusion criteria

Inclusion criteria: Participants must meet all of the following criteria to be eligible for the study:Aged 18 years or olderCurrently enrolled as a Bachelor’s, Master’s, or PhD student at one of the nine participating universitiesSufficient proficiency in Dutch or EnglishSelf-reported mood problems, operationalized as a score of =10 on the Patient Health Questionnaire-9 (PHQ-9)

Exclusion criteria

Exclusion criteria: Participants will be excluded from the study if they do not respond to the intake call with a study researcher prior to the start of the intervention.

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is the level of self-reported depressive symptoms, measured using the Patient Health Questionnaire-9 (PHQ-9). The main study parameter is the change in PHQ-9 scores from baseline to follow-up (2 and 8 weeks post-randomization), compared between the intervention groups (Moodpep and SpiralUp!) and the waitlist control group.Outcomes will be assessed at three time points: baseline (T0), 2 weeks post-randomization (T1), and 8 weeks post-randomization (T2).

Secondary

MeasureTime frame
Secondary outcomes include: •    Perceived stress, measured using the Perceived Stress Scale (PSS-10), •    Behavioral activation, measured with the Behavioral Activation for Depression Scale (BADS), •    Participant satisfaction, assessed through the Client Satisfaction Questionnaire (CSQ-8) and the Working Alliance Inventory for guided internet interventions (WAI-I), •    Academic performance, measured via self-reported academic functioning and study outcomes. All outcomes will be assessed at three time points: baseline (T0), 2 weeks post-randomization (T1), and 8 weeks post-randomization (T2).

Countries

Netherlands

Contacts

Public ContactNN Nas

Vrije Universiteit

n.f.nas@vu.nl+4917684170827

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: May 1, 2026