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Improving a training for youth with depressive symptoms.

Optimizing a modular approach for youth with depressive symptoms - Optimizing a modular approach for youth with stress, anxiety, and depressive symptoms

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON58273
Enrollment
30
Registered
2025-12-04
Start date
2025-10-09
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Subclinical depression Depressive symptoms

Interventions

The STARr-training is a modular prevention program based on cognitive behavioral therapy for youth with depressive symptoms. The STARr-training consists of four modules that are based on the elements
In the current study, we assess the simplified, adapted STARr training. The workbooks contain less text, written at a B1 level, and include more examples that are more inclusive of cultural background

Sponsors

Zorgonderzoek Nederland (ZON)
Lead Sponsor

Eligibility

Age
12 Years to 64 Years

Inclusion criteria

Inclusion criteria: To be eligible to participate in this study, a subject needs to meet the following criteria: • Aged between 12 and 20 years old; • Register for the STARr training at one of the two organizations• Provided informed consent (if a participant is between 12 and 16 years old, their parent(s) should also provide consent)

Exclusion criteria

Exclusion criteria: A subject who meets any of the following criteria will be excluded from participation in this study: • When acute and severe suicidal thoughts and/or intentions occur, expressed as a score of 2 on CDI-2 item ‘a desire to kill oneself, if given the chance’ followed by a total score of 12 or higher on the suicide items of the VOZZ, the researcher will share this with the trainer. After that, the protocol of the organizations regarding suicidal ideation and intent will be followed. The participants are informed about sharing this information in the information letter and are asked for consent in the informed consent letter.

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is the mean level difference of depressive symptoms between the baseline  phase and the effect phase. 

Secondary

MeasureTime frame
Secondary outcomes are mean level differences of anxiety, stress, and individual and societal functioning.

Countries

Netherlands

Contacts

Public ContactD. Bodden

Universiteit Utrecht

d.bodden@uu.nld.bodden@uu.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 3, 2026