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De klinische studie NCT07130734 (DPA) voor Depression - Major Depressive Disorder, angst, Stress is recruterend. Bekijk de kaartweergave van de Klinische Studies Radar en de AI-ontdekkingstools voor alle details. Of stel hier een vraag.
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Kaartweergave

Digital Intervention for Physical Activity (DPA)

Recruterend
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De klinische studie NCT07130734 (DPA) is een interventioneel studie bij Depression - Major Depressive Disorder, angst, Stress met de status recruterend. Het doel is om 50 deelnemers te includeren vanaf 22 september 2025. De studie wordt geleid door Auburn University en de voltooiing is gepland op 1 mei 2026. Laatste update op ClinicalTrials.gov: 18 september 2025.
Beknopte samenvatting

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
Uitgebreide beschrijving
Procedures include four laboratory visits: two visits before the intervention and two visits after the intervention.

Participants will be randomly assigned to either four weeks of a digital intervention that prompts participants to engage in physical activity or a waitlist (passive) control condition. Participants will be randomized using a stratified approach using depressive symptoms and physical activity measured at pre-intervention as strata.

The digital intervention group will be instructed to download a Pathverse mobile application on their Apple or Android smartphone device. The Pathverse mobile application will be used as a research delivery platform that can send participants daily push notifications to engage in physical activity of their choice. During the second pre-intervention visit, each participant will select approximately five types of physical activity they find enjoyable that they would like to engage in over the four-week intervention. Participants will report on the physical activity they completed, along with the duration and intensity of each activity. Participants will have the choice of time of day as to when they would like to receive daily notifications on their device.

Members of the passive control group will be informed that their mental health will be monitored over four weeks as a control condition. After the study, they will be offered the digital PA intervention, if desired.

Officiële titel

Digitally-Delivered Intervention to Prompt Physical Activity

Aandoeningen
Depression - Major Depressive DisorderangstStress
Andere studie-ID's
  • DPA
  • 00000675
NCT-ID
Startdatum (Werkelijk)
2025-09-22
Laatste update geplaatst
2025-09-18
Verwachte einddatum
2026-05
Inschrijving (Geschat)
50
Studietype
Interventioneel
FASE
N.v.t.
Status
Recruterend
Trefwoorden
Physical Activity
Digital Intervention
Depression
Mobile Application
Primaire doel
Behandeling
Toewijzing
Gerandomiseerd
Interventiemodel
Parallel
Blindering
Dubbelblind
Armen / Interventies
Deelnemersgroep/StudiearmInterventie/Behandeling
ExperimenteelDigital Intervention Group
Participants allocated to this group will be instructed to download a Pathverse mobile application on their Apple or Android smartphone device. The Pathverse mobile application will be used to send participants daily push notifications to engage in physical activity of their choice. During on-boarding at pre-intervention, each participant will choose approximately five types of physical activity they find enjoyable that they would like to engage in throughout the four-week intervention. They will report on the physical activity they completed, along with the duration and intensity of each activity. Participants will have the choice of when they would like to receive their daily notifications on their smartphone device.
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.
Geen interventiePassive Control Group
Participants will be informed that their mental health will be monitored over four weeks as a control condition. After the study, they will be offered the digital PA intervention, if desired.
N.v.t.
Primaire uitkomst
UitkomstmaatBeschrijving van de uitkomstmaatTijdsbestek
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.
pre-intervention, at the two-week time point during the intervention, and immediately after the intervention
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.
pre-intervention and immediately after the intervention
Geschiktheidscriteria

Leeftijd van deelnemers
Volwassene
Minimumleeftijd
19 Years
Geslachten die in aanmerking komen voor de studie
Allen
  • 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

- Participants will not qualify for the current study if they do not meet the above inclusion criteria.
Auburn University logoAuburn University
Verantwoordelijke instantie
Christopher Brush, Hoofdonderzoeker, Assistant Professor, Auburn University
Centraal Contactpersoon
Contact: Christopher J Brush, Ph.D., 334-844-4483, [email protected]
Contact: Karly A Knudson, B.S., [email protected]
1 Studielocaties in 1 landen

Alabama

Kinesiology Building, Auburn, Alabama, 36849, United States
Administrator, Business & Admin Services School of Kinesiology, Contact, 334-844-1450, [email protected]
Recruterend