Under construction – not a live service
Sign in
Taking people in United StatesNo phase

Digital program encouraging physical activity for adults with depression symptoms

Tests a digital program prompting activity in adults with depressive symptoms.

Plain-language title generated from the registry record
Registry title: Digital Intervention for Physical Activity

Key facts

Where
Auburn, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 19 and 40 years old?

Source: NCT07130734, who can take part

Where in United States

  • Kinesiology BuildingAuburn, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Auburn University
Trial code
NCT07130734
Record updated
28 October 2026
Original description
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:Read full original descriptionShow less

Digitally-Delivered Intervention to Prompt Physical Activity

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

Inclusion: 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: Participants will not qualify for the current study if they do not meet the above inclusion criteria.

ClinicalTrials.gov NCT07130734