Digital Intervention for Physical Activity
Recruiting now · Not applicable
Conditions studied: Depression - Major Depressive Disorder, Anxiety, Stress
In brief
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
Key facts
- Study ID
- NCT07130734
- Run by
- Auburn University
- People needed
- 50
- Starts
- 2025-09-22
- Expected to finish
- 2026-05-01
- Last updated by the study team
- 2025-09-18
Who can join
Age: 19 and older, up to 40. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- Participants will not qualify for the current study if they do not meet the above inclusion criteria.
Where it is running
- Kinesiology Building — Auburn, Alabama, United States (enrolling)
Full record on ClinicalTrials.gov
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