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Effectiveness of a Guided Mobile App Intervention for Depression and Anxiety in University

Background: Symptoms of depression and anxiety are prevalent among Spanish university students. Minimally guided online interventions have shown promise in reducing symptomatology and preventing increased mental distress. There is a need to evaluate the effectiveness of guided preventive mental health interventions for

Condition(s)Depressive Symptoms, Anxiety
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryBackground: Symptoms of depression and anxiety are prevalent among Spanish university students. Minimally guided online interventions have shown promise in reducing symptomatology and preventing increased mental distress. There is a need to evaluate the effectiveness of guided preventive mental health interventions for depression and anxiety in university students. Methods: two-arm multicenter randomized controlled trial (RCT), addressed to undergraduate students from 6 public universities with symptoms of depression and/or anxiety. Students will be evaluated through an online survey assessing mental health problems, use of mental health services, sociodemographic variables, self-perceived health, childhood and adolescent adversities, recent stressful events, social networks, personality a
Who can participateInclusion Criteria: * Eligible participants are all undergraduate students at the 6 participating universities and students followed in the PROMES-U observational study * Having 18 years of age or more * Having literacy in Spanish * Having access to a smartphone (Android or Apple) * With mild or moderate depression and/or anxiety symptoms screened (i.e., depression (5≤ (PHQ-9) ≤14); and/or anxiety (5≤ GAD-7 ≤14). Exclusion Criteria: * Moderately severe or severe depression and/or anxiety (i.e., PHQ-9≥15 and/or GAD-7≥15) * High suicide risk * A history of severe psychiatric disorder (e.g., bipolar, psychosis) * Being on mental health treatment (i.e., medication, psychotherapy or other intervention) Students with high suicide risk will receive a clinical alert recommending them to visit a sp
Ages18 Years
SexAll
Lead sponsorUniversity of the Balearic Islands
LocationsPalma de Mallorca, Balearic Islands, Spain
Start date2024-10-25
NCT IDNCT06078007
Official listinghttps://clinicaltrials.gov/study/NCT06078007

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