Recruiting

Digital Intervention for Physical Activity

ClinicalTrials.gov IDNCT07130734

PhaseNA

Enrollment50

SponsorAuburn University

Age19 Years

SexALL

I'm interested View official listing

Conditions studied

Depression - Major Depressive Disorder, Anxiety, Stress

About this study

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

Interventions

Behavioral: Digital Physical Activity — The Pathverse mobile application platform will be downloaded on each participant's smartphone. Participants will be guided on how to download and use the application, as well as how to interact with the application during the intervention period. Participants will choose approximately five types of physical activity they enjoy before the intervention and will be prompted to complete these physical activities throughout the intervention. Participants will also self-report the duration and type of physical activity performed each day of the intervention.

Primary outcomes

Depressive Symptoms (pre-intervention, at the two-week time point during the intervention, and immediately after the intervention)
Moderate-to-vigorous physical activity (pre-intervention and immediately after the intervention)

Eligibility information

Inclusion Criteria: * Between the ages of 19 and 40 years * Verbally fluent in English (i.e., must be able to speak or understand English) * No uncorrected visual or hearing impairment * Moderate depressive symptoms or greater of at least 10 or higher on the Patient Health Questionnaire-8 screening instrument * Eligible to participate in physical activity * Physically inactive (i.e., engaging in less than 150 min of weekly moderate-to-vigorous physical activity) * Owns an Apple or Android mobile device, willing to download the Pathverse app , and willing to keep the device on during the study period * Not currently pregnant Exclusion Criteria: \- Participants will not qualify for the current study if they do not meet the above inclusion criteria.

Study locations

Kinesiology Building, Auburn, Alabama 36849 United States

Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.

Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-09-27.