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A Mobile App to Address Student Loneliness

Using a Mobile App to Address Student Loneliness Among College Students: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04164654
Enrollment
221
Registered
2019-11-15
Start date
2019-09-09
Completion date
2021-05-06
Last updated
2022-09-15

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

Conditions

Loneliness

Brief summary

The purpose of this trial is to assess the effects of a positive psychology and CBT-based skills intervention-delivered through a mobile app called Nod-on loneliness and other mental health and institutional satisfaction outcomes. The primary outcome is self-reported loneliness at 2 and 4-weeks post baseline.

Detailed description

This study is a pilot eight-week randomized controlled intervention. It employs a waitlist control strategy for the first 4 weeks of the study (considered to be the active study period). Randomization will be to one of two conditions: 1. Experimental group: Immediate access to the Nod app 2. Waitlist control group: Participants will be granted access to the app four weeks after the experimental group Assessments will occur at baseline, 2, 4, and 8 weeks follow up. Assessments will include measures of loneliness, and other mental health and institutional satisfaction measures listed in the secondary outcome measures section.

Interventions

BEHAVIORALLoneliness Intervention

28 days of engagement with the Nod app, which consists of interactive exercises drawn from cognitive behavioral therapy (e.g behavioral activation and cognitive reframing exercises), positive psychology (e.g. acts of kindness), and mindful self-compassion programs (e.g. loving-kindness meditations)

Sponsors

HopeLab Foundation
CollaboratorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
University of Oregon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Incoming college first years * Live away from home without parents/guardians upon beginning college * Read English * Between 18 and 25 years of age * Own a smartphone

Exclusion criteria

* Do not read English * Under 18 years of age * Over 25 years of age * Do not own a smartphone

Design outcomes

Primary

MeasureTime frameDescription
Condition differences in self-reported loneliness2-weeks post baselineTotal score on the UCLA-8. Scores range from 8-32, higher scores indicate worse depression.

Secondary

MeasureTime frameDescription
Depressive symptoms2 and 4 weeks post baselineTotal score on the Patient Health Questionnaire 9-item scale. Scores range from 0-27, higher scores indicate worse depression.
Anxiety2 and 4 weeks post baselineTotal score on the Generalized Anxiety Disorder 7-item scale. Scores range from 0-21, higher scores indicate worse anxiety.
Social Anxiety2 and 4 weeks post baselineTotal score on the Mini Social Phobia Inventory. Scores range from 0-12, higher scores indicate worse social anxiety.
Self-reported intention to remain enrolled at the University of Oregon in the next academic year2 and 4 weeks post baselineSelf-reported intention to remain enrolled at the University of Oregon in the next academic year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026