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Depression, Experiential Diversity, and Behavioral Novelty

Depression, Experiential Diversity, and Behavioral Novelty: A Mobile Sensing Experimental Paradigm

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05767554
Enrollment
77
Registered
2023-03-14
Start date
2023-04-21
Completion date
2024-03-31
Last updated
2024-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Depression

Keywords

Behavioral activation, Mobile sensing

Brief summary

The purpose of the study is to test whether changes in behavioral patterns are related to changes in depression. Depression is a psychological condition that involves persistent sad mood and/or an inability to enjoy pleasurable activities. Very stable behavioral patterns may be related to symptoms of depression. The aim of this study is to learn more about the relationship between symptoms of depression and behavioral patterns that are collected via global positioning system location data from a smart phone.

Interventions

BEHAVIORALBrief modified behavioral activation

The clinician will deliver psychoeducation about the nature of depression and the rationale behind the behavioral activation model (i.e. increasing level of activation can begin a positive feedback cycle of reward and improvements in mood state). Participants will be encouraged to add new, enjoyable activities to their daily schedules. Clinicians will emphasize the importance of novelty and increased engagement with the surrounding environment in the psychoeducational portion and in activity scheduling.

Sponsors

University of Texas at Austin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-25 * Possession and daily use of a smart phone * Able to speak and read English * Patient Health Questionnaire -8 (PHQ-8) \> 10 * Behavioral Activation for Depression (BADS) Activation Subscale \< 16 * Ability to complete all study procedures

Exclusion criteria

* Self-reported lifetime diagnosis of agoraphobia or bipolar disorder * Severe neurodevelopmental disorder * Major travel plans within study period

Design outcomes

Primary

MeasureTime frameDescription
Change in Patient Health Questionnaire-8 Total Score over 5 WeeksBaseline and 5 weeksLevel of depression symptoms assessed weekly by the Patient Health Questionnaire - 8 via smart phone survey. The PHQ-8 ranges from 0-24 with higher scores indicating more severe symptoms of depression.

Secondary

MeasureTime frameDescription
Change in Behavioral Activation for Depression Scale over 5 WeeksBaseline and 5 weeksLevel of behavioral activation as measured by the Behavioral Activation for Depression Scale (BADS). The BADS ranges from 0-150 with higher scores indicating better functioning.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026