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Evaluating an Online Wellness Intervention for Greek Adolescents

Evaluating an Online Single-session Intervention for Mental Health and Wellness of Greek Adolescents

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04815681
Enrollment
0
Registered
2021-03-25
Start date
2021-03-31
Completion date
2022-12-31
Last updated
2025-06-11

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

Conditions

Anxiety, Depressive Symptoms, Happiness

Brief summary

The investigators are evaluating the effects of an online single-session mental health intervention (the Common Elements Toolbox; COMET). To evaluate COMET, the investigators are conducting a randomized controlled trial with Greek adolescents attending high school in the Attica region in Greece. Students will be randomized to the COMET condition or to an active control condition. Primary outcome measures (depressive symptoms, anxiety symptoms, subjective well-being) will be measured at two weeks post-intervention and four weeks post-intervention. The investigators will evaluate COMET as a universal intervention (using the full sample) and as a targeted intervention (analyzing those who reported elevated depressive symptoms or anxiety symptoms at baseline).

Interventions

COMET is an online unguided self-help intervention that lasts approximately 40-50 minutes.

BEHAVIORALActive Control

The active control condition includes an online self-awareness program that lasts approximately 40-50 minutes. Participants in the control condition will receive access to the intervention after data collection for the study has been completed.

Sponsors

National and Kapodistrian University of Athens, Greece
CollaboratorUNKNOWN
University Mental Health, Neurosciences and Precision Medicine Research Institute Costas Stefanis, Greece
CollaboratorUNKNOWN
University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
13 Years to 20 Years
Healthy volunteers
Yes

Inclusion criteria

* Between 13 and 20 years old and a student at a participating Greek high school. Access to the internet.

Design outcomes

Primary

MeasureTime frameDescription
Change in Patient Health Questionnaire-8 (PHQ-8)Up to 4 weeks post-interventionDepression questionnaire. Scores range from 0 to 24. Lower scores indicate less depression.
Change in Generalized Anxiety Disorder Screener-7 (GAD-7)Up to 4 weeks post-interventionAnxiety questionnaire. Total scores range from 0-21. Lower scores indicate less anxiety.
Change in the Short Warwick-Edinburgh Mental Well-being Scale (SWEMWBS)Up to 4 weeks post-interventionSubjective Well-being questionnaire. Total scores range from 7 to 35. Higher values indicate higher well-being scores.

Secondary

MeasureTime frameDescription
Perceived UtilityImmediately after interventionParticipants will be asked to rate three items relating to the perceived utility of each module. Specifically, the investigators asked participants: How helpful the module was; How engaging the module was; How much they will continue applying content from the module. If items are at least moderately correlated (r \> .5) the investigators will combine them in a single measure of perceived utility. Higher scores indicate greater perceived utility.
Ratings on the Acceptability of Intervention Measure (AIM)Immediately after the interventionQuestionnaire measuring the acceptability of an intervention. Acceptability refers to the perception that a given treatment is agreeable or satisfactory. The total score ranges from 4 to 20. Higher scores indicate higher acceptability ratings.
Positive and Negative Affect Schedule (PANAS)Up to 4 weeks post-interventionQuestionnaire measuring positive affect and negative affect. Scores on the positive affect subscale range from 10-50, with higher scores representing higher levels of positive affect. Scores on the negative affect subscale range from 10-50, with lower scores representing lower levels of negative affect.
Ratings on the Intervention Appropriateness Measure (IAM)Immediately after the interventionQuestionnaire measuring the appropriateness of an intervention. Appropriateness refers to the perceived fit or relevance of an intervention. The total score ranges from 4 to 20. Higher scores indicate higher appropriateness.
Secondary ControlUp to 4 weeks post-interventionThe investigators will ask participants three items to assess secondary control (Weisz et al., 2010). The items are scored on a 4-point Likert scale, ranging from 0 (Very false) to 3 (Very true). The three items are: When something bad happens, I can find a way to think about it that makes me feel better. After a really hard day, I can make myself feel better by remembering some good things that happened. When bad things happen to me that I can't control, there are lots of things I can do to feel better. Higher scores indicate greater secondary control.

Countries

Greece, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026