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NCT07130734Recruiting

Digital Intervention for Physical Activity

Digitally-Delivered Intervention to Prompt Physical Activity

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
11 Aug 2025
Start date
20 Oct 2025
Primary completion date
May 2027
Lead sponsor
Auburn University
Diseases
Depression
NCT number
NCT07130734

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 20 Oct 2025 to the primary completion date, May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \- Participants will not qualify for the current study if they do not meet the above inclusion criteria.

Who the study is looking for

  • 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

Age in the registry: 19 years to 40 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Kinesiology Building
Coordinator of this site? Confirm its status
AuburnUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.