Skip to content

Brief App-based Mood Monitoring and Mindfulness Intervention for First-year College Students

Brief App-based Mood Monitoring and Mindfulness Intervention for First-year College Students

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06348277
Enrollment
130
Registered
2024-04-04
Start date
2018-01-02
Completion date
2020-06-17
Last updated
2024-04-04

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

Conditions

Depression, Anxiety, Self-Injurious Behavior

Keywords

mindfulness, rumination, worry

Brief summary

The investigators examined whether brief, app-based interventions were helpful in alleviating mental health symptoms during the transition to college. In particular, the investigators were interested in whether a brief mobile-app mindfulness intervention combined with mood monitoring was more effective in alleviating first-year students' psychological distress than mood monitoring alone.

Detailed description

The transition to college is associated with worsening mental health symptoms. This study tested whether a brief mobile-app mindfulness intervention combined with mood monitoring was more effective in alleviating first-year students' psychological distress than mood monitoring alone. Participants were 130 first-year students. The investigators randomly assigned 88 students to a mindfulness-plus-mood-monitoring or a mood-monitoring-only group and asked them to use an app 3 times a day for 3 weeks. They, along with an assessment-only control group (n=42), completed self-report questionnaires at baseline, post-intervention, and 6 and 12 weeks later.

Interventions

BEHAVIORALMindfulness plus mood monitoring

mobile app that provides guided mindfulness exercises in addition to prompting for mood monitoring three times per day

BEHAVIORALMood monitoring

mobile app that prompts for mood monitoring three times per day

Sponsors

Lawrence University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* enrolled first-year student at university

Exclusion criteria

* serious suicidal concerns

Design outcomes

Primary

MeasureTime frameDescription
Worryimmediately after the interventionPenn State Worry Questionnaire; higher scores indicate greater worry
Depressive Symptomsimmediately after the interventionBeck Depression Inventory; higher scores indicate greater depression
Anxiety Symptomsimmediately after the interventionBeck Anxiety Inventory; higher scores indicate greater anxiety
Urges to Self-injureimmediately after the interventionAlexian Brothers Urges to Self-Injure scale; higher scores indicate greater urges
Ruminationimmediately after the interventionRuminative Response Scale; higher scores indicate higher rumination

Secondary

MeasureTime frameDescription
Depressive Symptoms6 weeks following the interventionBeck Depression Inventory; higher scores indicate greater depression
Anxiety Symptoms6 weeks following the interventionBeck Anxiety Inventory; higher scores indicate greater anxiety
Urges to self-injure6 weeks following the interventionAlexian Brothers Urges to Self-Injure scale; higher scores indicate greater urges
Rumination6 weeks following the interventionRuminative Response Scale; higher scores indicate higher rumination
Worry6 weeks following the interventionPenn State Worry Questionnaire; higher scores indicate greater worry

Countries

United States

Outcome results

None listed

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