Evidence map›Paper›PMID 39012691›Full record

ArticleJMIR research protocols2024

Identifying Person-Specific Drivers of Depression in Adolescents: Protocol for a Smartphone-Based Ecological Momentary Assessment and Passive Sensing Study.

Mei Yi Ng, Jennifer A Frederick, Aaron J Fisher, Nicholas B Allen, Jeremy W Pettit, Dana L McMakin

Abstract read
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Article in JMIR research protocols, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Mei Yi NgDepartment of Psychology and Center for Children and Families, Florida International University, Miami, FL, United States.ORCID 0000-0002-1399-0133
Jennifer A FrederickDepartment of Psychology and Center for Children and Families, Florida International University, Miami, FL, United States.ORCID 0000-0001-9411-4284
Aaron J FisherDepartment of Psychology, University of California, Berkeley, Berkeley, CA, United States.ORCID 0000-0001-9754-4618
Nicholas B AllenDepartment of Psychology, University of Oregon, Eugene, OR, United States.ORCID 0000-0002-1086-6639
Jeremy W PettitDepartment of Psychology and Center for Children and Families, Florida International University, Miami, FL, United States.ORCID 0000-0002-7426-9411
Dana L McMakinDepartment of Psychology and Center for Children and Families, Florida International University, Miami, FL, United States.ORCID 0000-0002-6954-4204

Funding

Identifying Person-Specific Drivers of Adolescent Depression via Idiographic Network Modeling of Active and Passive Smartphone DataR21MH126394 · NIMH · FLORIDA INTERNATIONAL UNIVERSITY · PI NG, MEI YI · 2021 to 2022
$422k
NIMH NIH HHS R21 MH126394
6 · The paper itself

Abstract

backgroundAdolescence is marked by an increasing risk of depression and is an optimal window for prevention and early intervention. Personalizing interventions may be one way to maximize therapeutic benefit, especially given the marked heterogeneity in depressive presentations. However, empirical evidence that can guide personalized intervention for youth is lacking. Identifying person-specific symptom drivers during adolescence could improve outcomes by accounting for both developmental and individual differences.

objectiveThis study leverages adolescents' everyday smartphone use to investigate person-specific drivers of depression and validate smartphone-based mobile sensing data against established ambulatory methods. We describe the methods of this study and provide an update on its status. After data collection is completed, we will address three specific aims: (1) identify idiographic drivers of dynamic variability in depressive symptoms, (2) test the validity of mobile sensing against ecological momentary assessment (EMA) and actigraphy for identifying these drivers, and (3) explore adolescent baseline characteristics as predictors of these drivers.

methodsA total of 50 adolescents with elevated symptoms of depression will participate in 28 days of (1) smartphone-based EMA assessing depressive symptoms, processes, affect, and sleep; (2) mobile sensing of mobility, physical activity, sleep, natural language use in typed interpersonal communication, screen-on time, and call frequency and duration using the Effortless Assessment of Risk States smartphone app; and (3) wrist actigraphy of physical activity and sleep. Adolescents and caregivers will complete developmental and clinical measures at baseline, as well as user feedback interviews at follow-up. Idiographic, within-subject networks of EMA symptoms will be modeled to identify each adolescent's person-specific drivers of depression. Correlations among EMA, mobile sensor, and actigraph measures of sleep, physical, and social activity will be used to assess the validity of mobile sensing for identifying person-specific drivers. Data-driven analyses of mobile sensor variables predicting core depressive symptoms (self-reported mood and anhedonia) will also be used to assess the validity of mobile sensing for identifying drivers. Finally, between-subject baseline characteristics will be explored as predictors of person-specific drivers.

resultsAs of October 2023, 84 families were screened as eligible, of whom 70% (n=59) provided informed consent and 46% (n=39) met all inclusion criteria after completing baseline assessment. Of the 39 included families, 85% (n=33) completed the 28-day smartphone and actigraph data collection period and follow-up study visit.

conclusionsThis study leverages depressed adolescents' everyday smartphone use to identify person-specific drivers of adolescent depression and to assess the validity of mobile sensing for identifying these drivers. The findings are expected to offer novel insights into the structure and dynamics of depressive symptomatology during a sensitive period of development and to inform future development of a scalable, low-burden smartphone-based tool that can guide personalized treatment decisions for depressed adolescents. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/43931.

Indexed as

DepressionEcological Momentary AssessmentSmartphoneActigraphyAdolescentFemaleHumansMaleMobile Applicationsactigraphyadolescentsdepressiondigital phenotypingecological momentary assessmentidiographic assessmentmobile sensingnetwork modelingsmartphonestreatment personalization

Identifiers

PMID39012691
PMCPMC11289582

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.