ClinicalTrials.gg
CompletedNCT06224647Updated Aug 28, 2024

Evaluation of a Transdiagnostic Mobile App Intervention Among University Students

An interventional study of Mobile Transdiagnostic Emotion Regulation Intervention in Emotion Regulation, Stress and Resilience, sponsored by Erasmus University Rotterdam. Completed at 1 site in Netherlands. Open to participants aged 18 Years to 32 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-08-28.

Sponsored by Erasmus University Rotterdam · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
202
Allocation
Randomized
Ages
18 Years to 32 Years
Sex
All
01

Study summary

This study is a two-armed randomized controlled trial (RCT) aimed at evaluating the effectiveness and adoption of a transdiagnostic mobile app intervention that focuses is on enhancing adaptive emotional regulation (ER) skills among university students.

Read the detailed description

Globally, an estimated 30% of university students struggle with mental health issues, primarily anxiety, depression, and substance abuse. Recent trends have highlighted the potential of online interventions for accessible, low-threshold support in preventing these issues among this demographic.

At Erasmus University Rotterdam (EUR), a transdiagnostic mobile app is being developed as part of a student wellbeing program. This app provides a range of tools aimed at improving mental health by teaching students adaptive emotional regulation strategies. It incorporates exercises from various therapeutic modalities, addressing factors like negative thoughts, rumination, and prolonged negative emotions. Delivered through a smartphone, the app includes 24 therapeutic exercises focusing on techniques such as enhancing positive emotions, mindfulness, cognitive defusion, cognitive restructuring, relaxation, breathing, and self-compassion.

The present study is a 12-week two-armed RCT study with outcomes assessed at the baseline, and three follow-ups at weeks 3, 8, and 12. It compares a group of distressed students with access to the mobile app intervention against a waitlist control group.

The main goal of the study is to assess the impact of the intervention on stress symptoms and emotional regulation skills. The secondary outcomes of the study, include an evaluation of the intervention's impact on depression, anxiety symptoms, and students' resilience levels. Lastly, the study examines the app's uptake, including engagement patterns and user experiences, and evaluates the real-life application of the skills learned through the app.

02

Conditions studied

  • Emotion Regulation
  • Stress
  • Resilience
  • Depressive Symptoms
  • Anxiety

Keywords

  • Transdiagnostic intervention
  • Digital intervention
  • Mental health
  • University Students
  • Randomized Controlled Trial
03

In context

Emotional Regulation

239 studies on the registry are indexed under Emotional Regulation; 124 are open to participants now.

This study's enrollment of 202 is above the median of 75 across 226 interventional studies indexed under Emotional Regulation.

Browse Emotional Regulation studies →

Lead sponsor

Erasmus University Rotterdam is the lead sponsor of 4 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 32 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Willing to participate and provide informed consent
  • Access to smartphone and internet
  • Feels comfortable with English language for verbal and written communication and interaction with the app
  • Scores \<13 on the Perceived Stress Scale (PSS-10)

Exclusion criteria

Exclusion Criteria:

  • Scores >20 on the Patient Health Questionnaire (PHQ-9)
  • Having a medical diagnosis of psychosis or bipolar disorder, severe clinical depression or anxiety disorder
  • Undergoing psychopharmacological treatment or treatment with experimental drugs
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
202 participants (actual)

Study arms

  • Experimental
    Access to the intervention

    Participants assigned to the intervention group will have full access to the mobile app intervention, namely ROOM app, for the whole duration of the 12-week trial. As part of the app's onboarding process, participants will receive tips on optimal app usage and can decide to take part in a 21-day challenge where they are encouraged to assess their emotional states on a daily basis and complete one exercise per day. During the onboarding process, participants are encouraged to explore different emotional regulation exercises offered in the app and to save the ones they find most beneficial in their "virtual Room", curating a personalized well-being toolkit. While daily notifications prompt regular app engagement, no additional efforts are made to further promote its use.

    Behavioral: Mobile Transdiagnostic Emotion Regulation Intervention

  • No intervention
    Waitlist control condition

    Participants allocated to the control group will be put on a waitlist and granted access to the mobile intervention after the trial concludes. They will then receive the same intervention with the identical onboarding process as the intervention group.

Interventions

  • BehavioralMobile Transdiagnostic Emotion Regulation Intervention

    The intervention aims to provide a tailored and engaging way for users to manage and comprehend their emotional well-being. It consist of 5 components: 1. Daily tracking of emotions 2. A suite of exercises placed in six categories facilitating adaptive emotion regulation skills (i.e., upregulation of positive effect, self-compassion, cognitive defusion and cognitive restructuring, mindfulness, breathing techniques), 3. A self-assessment module where users can complete surveys evaluating their states (e.g., wellbeing) and traits (e.g., perfectionistic tendencies), 4. A personal toolkit area (i.e., each exercise is represented by an object commonly found in a student's room. Users can collect objects of favoured exercises in the virtual ROOM, enabling them quick access to exercises they liked / found helpful), 5. A recommendation system linking users to the content based on their specific needs or preferences

    Also known as: ROOM app

06

What researchers measure

Primary outcomes

  1. Changes in stress symptoms

    Perceived Stress Scale (PSS-10) is used to evaluate participants' stress levels. Participants are asked to specify how often they felt or thought a certain way over the last month on a scale from 0 \[never\] to 5 \[very often\]. The score ranges from 0 - 40, with higher scores indicating higher levels of perceived stress symptoms.

    Time frame: At baseline and days 21, 56, and 84.

  2. Changes in ER skills

    The Emotion Regulation Skills Questionnaire (ERSQ) will be used to assess emotion regulation skills. This instrument includes seven distinct emotion regulation skills: awareness, sensation, clarity, understanding, acceptance, tolerance, compassionate self-support, confrontation readiness, and modification of negative emotions. It consists of 27 items, each scored on a scale ranging from 0 (not at all) to 4 (almost always). Higher scores on both the ERSQ subscales and the aggregate ERSQ score are indicative of higher emotion regulation skills.

    Time frame: At baseline, and days 56 and 84.

Secondary outcomes

  1. Changes in depressive symptoms

    Depressive symptoms are measured with the Patient Health Questionnaire (PHQ-9). Participants are asked to indicate how often they have been bothered by a certain symptom over the past two weeks on a scale from 0 (not at all) to 3 (nearly every day). PHQ-9 scores range from 0-27. Higher scores indicate higher levels of depressive symptoms.

    Time frame: At baseline and day 84

  2. Changes in anxiety symptoms

    Anxiety symptoms are measured with the Generalized Anxiety Disorder (GAD-7) questionnaire. Participants are asked to indicate how often they have been bothered by a certain symptom over the last two weeks on a scale from 0 (not at all) to 3 (nearly every day). The scores on GAD-7 range between 0-21, with higher scores indicating higher levels of anxiety.

    Time frame: At baseline and day 84

  3. Changes in resilience levels

    Resilience levels are evaluated with the 10-item Connor-Davidson Resilience Scale (CD-RISC-10). Items are scored on a scale ranging from 0 (not true at all) to 4 (true nearly all the time). Total scores range between 0 and 40 with higher scores indicating greater resilience.

    Time frame: At baseline and day 84

  4. Objective engagement patterns

    Objective engagement patterns include exercise completion and non-completion (i.e., exercise started but not finished) rates, average time spent on each exercise, engagement in self-assessment module (i.e., number of questionnaires and Ecological Momentary Assessments completed), the number of objects collected in the "virtual room", the number of times the app was accessed. Log data is used to evaluate objective engagement patterns.

    Time frame: Day 1 - 84

  5. Subjective engagement: Exercise likeability and helpfulness

    Exercise likeability and helpfulness is evaluated on a 5-point Likert scale ranging from 1 (not at all) to 5 (very much) every time a participant completes an exercise. * How much did you like the exercise? * How helpful did you find the exercise?

    Time frame: Day 1-84

  6. Subjective engagement: Likeability and helpfulness of Self-assessment component

    The likeability and helpfulness of the Self-assessment module (MapMyself) is evaluated on a scale from 1 (not at all) to 5 (very much) * How much did you like the self-assessment (MapMyself) feature in the app? * How helpful did you find the self-assessment (MapMyself) feature in the app?

    Time frame: Day 56

  7. Subjective engagement: Likeabilty of Virtual Collectibles Room

    The likeability of the Virtual Collectibles Room component is assessed on a scale ranging from 1 (not at all) to 5 (very much) \- How much do you like collecting objects in the ROOM app?

    Time frame: Day 56

  8. Subjective engagement: Usefulness and perceived effectiveness of recommendation system

    Participants are asked to evaluate the recommendation system by rating the following two questions on a scale from 1 (not at all) to 5 (very much) * How useful do you find the in-app recommendations of the exercises? * How well do the in-app recommendations of exercises align with your self-reported moods?

    Time frame: Day 56

  9. Subjective engagement: User experience with the app

    User experiences are evaluated with a User Experience Questionnaire (UEQ) measuring the Attractiveness, Perspicuity, Efficiency, Dependability, and Novelty of the app. The questionnaire includes 26 items measured on a semantic differential (e.g., attractive - unattractive). The items are scored from -3 (the most negative answer) to +3 (the most positive answer), with 0 representing a neutral answer.

    Time frame: Day 56

  10. Engagement with the exercises outside of the app: In app counter

    The mobile intervention includes a feature (i.e., an exercise counter) where users can log in the number of times they completed an exercise outside of the app. This counter is used to evaluate the number of exercises performed independently from the app.

    Time frame: Day 1-84

  11. Engagement with ER techniques outside of the app

    Participants are asked to evaluate how often they applied ER techniques (e.g., self-compassion, breathing pattern, savouring, being mindful, reframing unhelpful thoughts) in their daily life over the past month on a scale from 0 (not at all) - 4 (daily). \- Over the past month, how frequently have you spontaneously used any of the techniques you've learned in ROOM app either to manage your emotions during challenging times or to improve your overall mood?

    Time frame: Day 21, 56, 84

  12. Likability and helpfulness of transfer strategies offered in the app

    For evaluation of the learning transfer features in the app, participant will be asked to rate the following questions on a scale from (0 - Not at all; 100 - Very much or So far I haven't used this feature). * How much do you like action planning with 'when-then' statements? * How helpful do you find the action planning with 'when-then' statements? * How much do you like to use stickers to create cues to practice the techniques? * How helpful do you find stickers to create cues to practice the techniques? * How much do you like the 'practice semi-guided' feature of the app? * How helpful do you find the 'practice semi-guided' feature of the app?

    Time frame: Day 56

07

Study locations

1 site
  • Erasmus University Rotterdam
    Rotterdam, South Holland 3062 PA, Netherlands
08

References and documents

Publications

  • Laure T, Engels RCME, Remmerswaal D, Spruijt-Metz D, Konigorski S, Boffo M. Optimization of a Transdiagnostic Mobile Emotion Regulation Intervention for University Students: Protocol for a Microrandomized Trial. JMIR Res Protoc. 2023 Oct 27;12:e46603. doi: 10.2196/46603. PubMed 37889525 ↗

Individual participant data

Plan to share: Yes — Data [and code] produced in the project will be shared in a research data repository [EUR Data Repository (EDR) and Open Science Framework (OSF)]. A DCMI (Dublin Core Metadata Initiative) standard will be used to document this research. There will be a temporary restriction on re-using of the data (Embargo period of 6 months). Data (and code) that will be shared in a research data repository are: Anonymized survey data, Codebook and Blank Questionnaires, Readme text file (general description of the data, including date of collection, selection procedure of participants, tools used to collect the data etc.), and scripts of data analysis.

Supporting information: Study protocol, Statistical analysis plan, Clinical study report, Analytic code

Time frame: The data will come available after the embargo period of 6 months

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 28, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06224647
Lead sponsor
Erasmus University Rotterdam
Responsible party
Marilisa Boffo (Assistant professor of Clinical Psychology and eHealth, Erasmus University Rotterdam) — Principal investigator
First posted
Jan 25, 2024
Start date
Feb 5, 2024
Primary completion
Jul 1, 2024
Completion
Jul 1, 2024
Last update
Aug 28, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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