Evidence map›Paper›PMID 40312714›Full record

ArticleBMC psychiatry2025

Smartphone-based Monitoring and cognition Modification Against Recurrence of Depression (SMARD): An RCT of Memory Bias Modification Training vs. Cognitive Control Training vs. Attention Bias Modification Training in remitted recurrently depressed patients with 1.5 year follow-up.

N Ikani, A Tyborowska, N Kohn, N Günther, G J Siegle, A H Schene, J A S Vorstman, C J Harmer, M J Kas, J N Vrijsen and 1 more

Abstract readClinical Trial Protocol
In one paragraph

Article in BMC psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Observational
  2. Article
4 · The record

Corrections and comments

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

11 authors.

N IkaniDepartment of Psychiatry, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center, Nijmegen, The Netherlands. n.ikani@tilburguniversity.edu.
A TyborowskaDepartment of Psychiatry, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center, Nijmegen, The Netherlands.
N KohnCognitive Neuroscience Department, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center, Nijmegen, The Netherlands.
N GüntherDepartment of Psychiatry, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center, Nijmegen, The Netherlands.
G J SiegleDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA.
A H ScheneDepartment of Psychiatry, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center, Nijmegen, The Netherlands.
J A S VorstmanProgram in Genetics and Genome Biology, The Hospital for Sick Children Research Institute, Toronto, ON, Canada.
C J HarmerUniversity Department of Psychiatry, Warneford Hospital, Oxford, UK.
M J KasGroningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, The Netherlands.
J N VrijsenDepartment of Psychiatry, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center, Nijmegen, The Netherlands.
H G RuhéDepartment of Psychiatry, Donders Institute for Brain, Cognition and BehaviourRadboud University Medical Center, Nijmegen, The Netherlands.

Funding

Hersenstichting HA2015.01.07
6 · The paper itself

Abstract

backgroundMajor Depressive Disorder (MDD) has a 50-80% recurrence rate highlighting the urgent need for more efficient recurrence prevention programs. Currently, recurrences are often identified too late, while existing preventive strategies may not sufficiently address ethio-patho-physiological mechanisms for recurrence. Negative memory bias (the tendency to better remember negative than positive events), negative attention bias (selective attention favoring mood-congruent information), and cognitive control deficits are important factors involved in the onset, maintenance, and recurrence of depressive episodes.

methodsHere we describe the protocol for the Smartphone-based Monitoring and cognition Modification Against Recurrence of Depression (SMARD) study, aiming to investigate different forms of cognitive training programs administered via smartphones, in order to develop a second-generation recurrence prevention program. In addition, we will gather Experience Sampling Method (ESM) assessments during a 6-day period, and during the follow-up period we will obtain behavioral data on (social) activities with BEHAPP, a smartphone-based Mobile Passive Monitoring application for remote behavioral monitoring to identify behavioral changes indicative of an imminent depressive episode. In a randomized controlled trial, SMARD will compare the effects of a smartphone-based Memory Bias Modification Training (MBT), Cognitive Control Training (CCT), and Attention Bias Modification Training (ABT) versus cognitive domain-specific (active-) sham trainings in 120 remitted MDD-patients with recurrent-MDD. Over the course of three weeks, participants receive multiple daily training sessions. Thereafter, participants will be followed up for 1.5 years with 3-monthly interviews to assess recurrences. DISCUSSION: The SMARD study aims to 1. assess the effects of the cognitive training programs versus their training-specific (active-) sham conditions on changes in memory, cognitive control dysfunction and attention; 2. relate training effects to neural networks previously identified in (recurrence of) MDD (therefore we obtain functional Magnetic Resonance Imaging ((f)MRI) scans before and after the training in a subset of participants); 3. link baseline and change in memory, cognitive control, attention and neural functioning, and ESM data to prospective recurrences; 4. examine whether passive smartphone-use monitoring can be used for prediction of recurrences.

trial registrationNL-OMON26184 and NL-OMON27513. Registered 12 August 2021-Retrospectively registered,  https://onderzoekmetmensen.nl/en/trial/26184 en https://onderzoekmetmensen.nl/en/trial/27513 .

Indexed as

Attentional BiasCognitive Behavioral TherapyMajor Depressive DisorderSecondary PreventionSmartphoneAdultAttentionFemaleFollow-Up StudiesHumansMaleMemoryMobile ApplicationsRandomized Controlled Trials as TopicRecurrenceCognitive biasCognitive trainingMajor depressive disorderNeural networksRecurrenceSmartphone-based mobile passive monitoring and modification

Identifiers

PMID40312714
PMCPMC12046686

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.