Actively Recruiting

Phase Not Applicable
Age: 19Years - 40Years
All Genders
NCT07130734

Digital Intervention for Physical Activity

Led by Auburn University · Updated on 2025-09-18

50

Participants Needed

1

Research Sites

31 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The present study will assess the effects of a four-week digitally delivered intervention on physical activity and depressive symptoms among adults experiencing at least moderate depressive symptoms. The main questions this research aims to answer are: * Does a digitally-delivered intervention increase physical activity levels? * Does a digitally-delivered intervention reduce symptoms of depression? Researchers will compare an intervention promoting physical activity to a passive control (does not receive the intervention) group to see if the intervention reduces depressive symptoms and increases physical activity levels. Participants will: * Visit the laboratory at two separate time points before group assignment, separated by one week of physical activity monitoring * Be randomly assigned to complete four weeks of a digital intervention prompting engagement in physical activity or have their mental health symptoms monitored over four weeks (i.e., passive control group) * Visit the laboratory at two separate time points after the intervention, separated by one week of physical activity monitoring

CONDITIONS

Official Title

Digital Intervention for Physical Activity

Who Can Participate

Age: 19Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Between the ages of 19 and 40 years
  • Verbally fluent in English (must be able to speak or understand English)
  • No uncorrected visual or hearing impairment
  • Moderate depressive symptoms or greater with a Patient Health Questionnaire-8 score of 10 or higher
  • Eligible to participate in physical activity
  • Physically inactive, engaging in less than 150 minutes of weekly moderate-to-vigorous physical activity
  • Owns an Apple or Android mobile device and willing to download and use the Pathverse app during the study
  • Not currently pregnant
Not Eligible

You will not qualify if you...

  • Does not meet all the above inclusion criteria

AI-Screening

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Trial Site Locations

Total: 1 location

1

Kinesiology Building

Auburn, Alabama, United States, 36849

Actively Recruiting

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Research Team

C

Christopher J Brush, Ph.D.

CONTACT

K

Karly A Knudson, B.S.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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