Evidence map›Paper›PMID 42330698›Full record

ArticleJournal of psychiatric research2026

Balancing burden and resolution: Effects of EMA survey schedule on compliance and study evaluation in suicide-focused research.

Miguel Blacutt, Connor M O'Brien, Ross Jacobucci, Brooke A Ammerman

Abstract read
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Article in Journal of psychiatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Miguel BlacuttDepartment of Psychology, University of Notre Dame, Corbett Family Hall, 18931 Moose Krause Cir, Notre Dame, IN, 46556, United States. Electronic address: mblacutt@nd.edu.
Connor M O'BrienDepartment of Psychology, University of Wisconsin - Madison, Brogden Hall, 1202 W Johnson St, Madison, WI, 53706, United States. Electronic address: cmobrien7@wisc.edu.
Ross JacobucciCenter for Healthy Minds, University of Wisconsin - Madison, 625 W Washington Ave, Madison, WI, 53703, United States. Electronic address: jacobucci@wisc.edu.
Brooke A AmmermanDepartment of Psychology, University of Wisconsin - Madison, Brogden Hall, 1202 W Johnson St, Madison, WI, 53706, United States. Electronic address: baammerman@wisc.edu.

Funding

Advancing Real-Time Suicide Risk Detection Through the Digital Phenotyping Smartphone Application ScreenomicsR21MH129688 · NIMH · UNIVERSITY OF NOTRE DAME · PI AMMERMAN, BROOKE A, JACOBUCCI, ROSS · 2022 to 2023
$430k
Improving momentary suicide risk identification through adaptive time samplingR21MH131978 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI AMMERMAN, BROOKE A, JACOBUCCI, ROSS · 2023 to 2024
$418k
NIMH NIH HHS R21 MH129688NIMH NIH HHS R21 MH131978
6 · The paper itself

Abstract

INTRODUCTION/

backgroundEcological momentary assessment (EMA) enables fine-grained, real-time prediction and monitoring of suicidal ideation and related experiences, but participant burden and declining compliance pose challenges. This study examined how EMA survey schedules influence EMA compliance, response likelihood, and participant burden.

methodsParticipants (N = 137) with recent suicidal ideation completed 28 days of EMA under one of three schedules: fixed (six surveys/day), 4+burst (four/day with one week of 10/day), or randomly varying (3-15 surveys/day). Bayesian mixed-effects and logistic regression models examined the effects of schedule type and time on overall and momentary compliance. Associations between compliance and schedule type with perceived burden, emotional reactions, and satisfaction were examined.

resultsSchedule type was not associated with overall compliance; however, time-by-schedule interactions showed that 4+burst and randomly varying conditions exhibited less decline over time than the fixed condition. Prior survey completion increased momentary response likelihood, while time in study decreased the likelihood of responding. Higher compliance was associated with fewer perceived drawbacks; no other effects of compliance or study schedule were found. DISCUSSION: Although overall compliance did not differ across schedules, those that incorporated some variability in survey frequency showed more sustained compliance over time. Responding to the previous survey increased response likelihood, indicating a momentum effect, whereas longer study participation reduced momentary compliance, consistent with cumulative survey fatigue.

conclusionIncorporating variability in survey frequency sustained greater compliance over time without increasing perceived burden, suggesting that varying EMA schedules may help mitigate study fatigue.

Indexed as

Ecological Momentary AssessmentPatient ComplianceSuicidal IdeationAdolescentAdultBayes TheoremFemaleHumansMaleYoung AdultComplianceEcological momentary assessmentIntensive longitudinal designSuicidal ideationSuicideSurvey methodology

Identifiers

PMID42330698
PMCPMC13520070

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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.