Evidence map›Paper›PMID 30244687›Full record

ReviewCNS spectrums2019

Conducting clinical studies targeting cognition in psychiatry: guiding principles and design.

Tamsyn E Van Rheenen, Kathryn E Lewandowski, Jessica M Lipschitz, Katherine E Burdick

Open access · bronzeAbstract readReview
In one paragraph

Review in CNS spectrums, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. MICEmi: A method to identify cognitive endophenotypes of mental illnesses.European psychiatry : the journal of the Association of European Psychiatrists · 2022
    Review
  5. 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

4 authors at 3 institutions in 2 countries.

Tamsyn E Van Rheenen1Department of Psychiatry,Melbourne Neuropsychiatry Centre,University of Melbourne,Melbourne,Australia.
Kathryn E Lewandowski4Schizophrenia and Bipolar Disorder Program,McLean Hospital,Belmont,Massachusetts,USA.
Jessica M Lipschitz5Department of Psychiatry,Harvard Medical School,Boston,Massachusetts,USA.
Katherine E Burdick5Department of Psychiatry,Harvard Medical School,Boston,Massachusetts,USA.
Brigham and Women's Hospital · USHarvard University · USMonash University · AU

Funding

Understanding the Neurocognitive Heterogeneity in Bipolar DisorderR01MH100125 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BURDICK, KATHERINE ELIZABETH · 2013 to 2017
$2.1M
1/2-Pramipexole in Bipolar Disorder:Targeting Cognition (PRAM)-BDR01MH102257 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BURDICK, KATHERINE ELIZABETH · 2014 to 2016
$1.2M
Neurocognitive Heterogeneity in Patients with Psychosis _ A Dimensional ApproachI01CX000995 · VA · JAMES J PETERS VA MEDICAL CENTER · PI BURDICK, KATHERINE ELIZABETH · 2014 to 2019
–
CSRD VA I01 CX000995NIMH NIH HHS R01 MH100125NIMH NIH HHS R01 MH102257
6 · The paper itself

Abstract

Cognitive dysfunction is common in many psychiatric disorders. While it has long been described as a core feature in schizophrenia, more recent data suggest qualitatively similar impairments in patients with bipolar disorder and major depressive disorder. There is compelling evidence to suggest that cognitive impairment contributes directly to functional disability and reduced quality of like across these disorders. As current treatments focus heavily on "primary" symptoms of mood and psychosis, the standard of care typically leaves cognitive deficits unmanaged. With this in mind, the field has recently begun to consider intervening directly on this important symptom domain, with several ongoing trials in schizophrenia. Fewer studies have targeted cognition in bipolar disorder and still fewer in MDD. With progress toward considering this domain as a target for treatment comes the need for consensus guidelines and methodological recommendations on cognitive trial design. In this manuscript, we first summarize the work conducted to date in this area for schizophrenia and for bipolar disorder. We then begin to address these same issues in MDD and emphasize the need for additional work in this area.

Indexed as

CognitionAntipsychotic AgentsBipolar DisorderClinical Trials as TopicHumansMajor Depressive DisorderNootropic AgentsSchizophreniaAntipsychotic AgentsNootropic AgentsBipolar disorderclinical trialcognitiondepressionschizophreniatreatment

Identifiers

PMID30244687
PMCPMC6414246
OpenAlexW2893953981

What OpenQuestion holds

Textmetadata
LicenceTDM
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.