Digital Intervention for Physical Activity

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19-40
SponsorAuburn University

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Digital Physical Activity

    Behavioral

    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.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Digital Intervention GroupExperimental treatment 1 intervention
Group B: Passive Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Depressive Symptoms

Depression, Anxiety, and Stress Scale (DASS-21) will be used to assess changes in symptoms of depression. The DASS-21 includes 7 items that assess for depression. Total scores for depression range from 0-42, with higher scores indicating greater depression severity.

Time frame
pre-intervention, at the two-week time point during the intervention, and immediately after the intervention
2

Moderate-to-vigorous physical activity

Physical activity will be assessed using a wrist-worn accelerometer before and after the intervention. Physical activity outcomes will be calculated as amount of time spent in a specific intensity.

Time frame
pre-intervention and immediately after the intervention

Secondary outcomes

Other outcomes

Sponsors and contacts

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