Actively Recruiting
Effectiveness of a Guided Mobile App Intervention for Depression and Anxiety in University Students (PROMES-U Study)
Led by University of the Balearic Islands · Updated on 2024-10-31
600
Participants Needed
1
Research Sites
53 weeks
Total Duration
On this page
Sponsors
U
University of the Balearic Islands
Lead Sponsor
H
Hospital del Mar Research Institute (IMIM)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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 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 and university experiences. A total of 600 students will be randomly assigned to: intervention group (guided E-health prevention intervention) or control group (treatment as usual with self-monitoring). The intervention, in app format, is based on principles of cognitive behavioral therapy, includes weekly feedback based on content and participation from a psychologist and self-monitoring. Assessments will take place post-intervention (up to 6 weeks), at 6 months and 12 months after randomization. The primary outcome will be the reduction of depressive or anxiety symptoms post-intervention, assessed with the Patient Health Questionnaire-9 (PHQ-9), the Generalized Anxiety Disorder-7 (GAD-7) and the Patient Health Questionnaire-Anxiety and Depression Scale (PHQ-ADS). Secondary outcomes of the RCT will be mental wellbeing, academic stress, comorbid symptoms, and adherence. Analyses will be conducted on an intention-to-treat and per protocol basis. Discussion: The results of the PROMES-U RCT will provide valuable information on a guided preventive online intervention that could be delivered in the campus context. In addition, results will provide information on the positive impact of the intervention on other relevant factors involved in mental health among university students.
CONDITIONS
Official Title
Effectiveness of a Guided Mobile App Intervention for Depression and Anxiety in University Students (PROMES-U Study)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be an undergraduate student at one of the six participating universities or in the PROMES-U observational study
- Be 18 years of age or older
- Be literate in Spanish
- Have access to a smartphone (Android or Apple)
- Have mild or moderate depression and/or anxiety symptoms (PHQ-9 score between 5 and 14 and/or GAD-7 score between 5 and 14)
You will not qualify if you...
- Have moderately severe or severe depression and/or anxiety (PHQ-9 score 15 or higher and/or GAD-7 score 15 or higher)
- Have a high suicide risk
- Have a history of severe psychiatric disorders such as bipolar disorder or psychosis
- Currently be receiving mental health treatment including medication, psychotherapy, or other interventions
AI-Screening
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Trial Site Locations
Total: 1 location
1
Miquel Roca
Palma de Mallorca, Balearic Islands, Spain, 07122
Actively Recruiting
Research Team
J
Jordi Alonso
CONTACT
P
PROMES-U Study
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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