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The Lived Experiences Measured Using Rings Pilot Study (LEMURS-P)

University of Vermont logo

University of Vermont

Status and phase

Completed
Phase 2

Conditions

Depression
Anxiety
Sleep
Stress

Treatments

Behavioral: Nature Experiences
Behavioral: Physical Activity
Behavioral: Moodlifters

Study type

Interventional

Funder types

Other

Identifiers

NCT05841979
LEMURS S23

Details and patient eligibility

About

The transition to college is a period of elevated risk for a range of mental health conditions. For students with pre-existing mental health diagnoses, the added pressures can exacerbate challenges. Although colleges and universities strive to provide mental health support to their students, the high demand for these services makes it difficult to provide scalable cost-effective solutions. To address these issues, the present study aims to compare the efficacy of three different treatments using a large cohort of 600 students transitioning to college. Interventions were selected based on their potential for generalizability and cost-effectiveness on college campuses. The randomized controlled trial will assign 150 participants to one of four arms: 1) group-based therapy, 2) physical activity program, 3) nature experiences group, or 4) self-monitoring condition as the control group. In addition, biometric data will be collected from all participants using a wearable device to develop algorithmic predictions of mental and physical health functioning. Once recruitment is complete, modeling strategies will be used to evaluate the outcomes and effectiveness of each intervention. The findings of this study will provide evidence as to the benefits of implementing scalable and proactive interventions using technology with the goal of improving well-being and success of new college students.

Enrollment

188 patients

Sex

All

Ages

18 to 25 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Current undergraduate student in their first year of school
  • own a mobile device

Exclusion criteria

  • None

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

188 participants in 4 patient groups

group-based therapy
Experimental group
Description:
Group therapy delivered via moodlifters
Treatment:
Behavioral: Moodlifters
physical activity
Experimental group
Description:
Physical Activity and Exercise
Treatment:
Behavioral: Physical Activity
nature experience
Experimental group
Description:
Nature Experiences
Treatment:
Behavioral: Nature Experiences
self-monitoring
No Intervention group
Description:
Placebo control

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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