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Longitudinal Well-Being Study

F

Flourish Science, Inc.

Status

Not yet enrolling

Conditions

Healthy

Treatments

Device: Digital toolkit
Other: National mental health resources

Study type

Interventional

Funder types

Industry

Identifiers

NCT06668532
Flourish2024-01

Details and patient eligibility

About

The goal of this clinical trial is to evaluate the effectiveness of the Flourish app-a digital toolkit providing science-based well-being practices-in enhancing mental health among students. The main questions it aims to answer are:

  • Does regular use of the Flourish app improve well-being, emotional resilience, and stress management?
  • Is more frequent use of the Flourish app associated with greater improvements in these outcomes?

Researchers will compare outcomes between participants using the Flourish app and a control group receiving curated national mental health resources to assess the app's impact.

Participants will:

  • Complete an initial 15-minute survey to establish baseline mental health
  • Those in the Flourish app condition will use the app at least twice weekly, while those in the control condition will receive weekly mental health resources and reflect on their application
  • Complete biweekly follow-up surveys over six weeks, with a final survey three months later

Enrollment

200 estimated patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Currently a student
  • Fluent in English
  • No uncontrolled mental health condition that significantly impacts daily life
  • Prolific approval rate within the 95-100% range
  • Minimum of 20 previous Prolific submissions

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

200 participants in 2 patient groups

Flourish app condition
Experimental group
Description:
Participants in this condition will gain access to the Flourish app and be instructed to use it at least twice a week for 6 weeks.
Treatment:
Device: Digital toolkit
Control Condition
Active Comparator group
Description:
Participants in the control condition will gain access to mental health resources each week for 6 weeks and be instructed to reflect on how the information in the resources can be applied to their own lives.
Treatment:
Other: National mental health resources

Trial contacts and locations

0

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Central trial contact

Xuan Zhao, PhD; Julie Y Cachia, PhD

Data sourced from clinicaltrials.gov

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