Evidence map›Paper›PMID 32423941›Full record

ArticleBMJ open2020

Internet-based cognitive-behavioural therapy for prevention of depression during pregnancy and in the post partum (iPDP): a protocol for a large-scale randomised controlled trial.

Daisuke Nishi, Kotaro Imamura, Kazuhiro Watanabe, Erika Obikane, Natsu Sasaki, Naonori Yasuma, Yuki Sekiya, Yutaka Matsuyama, Norito Kawakami

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
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

19 citing papers in PubMed, 32 citations in OpenAlex.

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  6. Time-varying restless legs syndrome and risk of incident perinatal depression.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2026
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  19. Perinatal mental health and COVID-19 in Japan.Psychiatry and clinical neurosciences · 2020
    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

9 authors at 1 institution in 1 country.

Daisuke NishiDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan d-nishi@m.u-tokyo.ac.jp.ORCID 0000-0001-9349-3294
Kotaro ImamuraDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Kazuhiro WatanabeDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Erika ObikaneDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Natsu SasakiDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Naonori YasumaDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID 0000-0002-1216-7639
Yuki SekiyaDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Yutaka MatsuyamaDepartment of Biostatistics, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
Norito KawakamiDepartment of Mental Health, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.ORCID 0000-0003-1080-2720
The University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe objective of this randomised controlled trial (RCT) is to examine the effects of smartphone-based cognitive-behavioural therapy (CBT) in preventing the onset of major depressive episodes (MDE) among pregnant women. METHODS AND ANALYSIS: The target study population will be pregnant women of 16-20 weeks gestation who are currently users of 'Luna Luna Baby', the most widely used app for pregnant women in Japan. Those who meet the eligibility criteria will be randomly allocated to the 6-module internet CBT programme that was newly developed for pregnant women (n=2500), or to a treatment-as-usual control group (n=2500). Participants in the intervention groups will be required to complete the programme by 32 weeks gestation. The primary outcomes are the number of new onsets of MDE, measured by using WHO Composite International Diagnostic Interview 3.0 at 32 weeks gestation and 3 months post partum. Survival analysis will be conducted to test for the effectiveness of the intervention on the time to the onset of MDE. ETHICS AND DISSEMINATION: The study plan has been approved by the Research Ethics Review Board of the Graduate School of Medicine/Faculty of Medicine, the University of Tokyo (2019150NI). If the intervention programmes are found to produce a significant positive effect in this RCT, these programmes can be made available for all users of the app in the future. TRIAL REGISTRATION NUMBER: UMIN000038190; Pre-results.

Indexed as

Cognitive Behavioral TherapyDepressionFemaleHumansInternetJapanPostpartum PeriodPregnancyRandomized Controlled Trials as Topicdepression & mood disordersmental healthpreventive medicine

Identifiers

PMID32423941
PMCPMC7239549
OpenAlexW3024025758

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.