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Antioksidansi za liječenje smanjene plodnosti u muškaraca

3 years 7 months ago
Antioksidansi za liječenje smanjene plodnosti u muškaraca Istraživačko pitanje Poboljšavaju li oralni antioksidansi kao dodaci prehrani uspješnost liječenja smanjene plodnosti u muškaraca, u usporedbi s placebom, izostankom liječenja ili drugim antioksidansima? Dosadašnje spoznaje Može se smatrati da par ima problema s plodnošću ako bezuspješno pokušava začeti više od godinu dana. Mnogi muškarci sa smanjenom plodnošću koji se liječe od neplodnosti uzimaju i dodatke prehrani u nadi da će im oni poboljšati plodnost. Liječenje neplodnosti može biti stresno razdoblje života, kako za muškarce...

Global Evidence Summit – Postponed to 9 – 13 September 2024

3 years 7 months ago

Dear Friends and Colleagues

Due to the continued global impact of COVID-19 (coronavirus) with ongoing reduced/restricted travel from many regions, and the advent of geo-political instability and risks in the European region, we have taken the decision to postpone the Global Evidence Summit (GES 2), due to be hosted in Prague between 2 – 6 October 2023.

The Global Organising Committee (comprising four partners:  Cochrane, JBI, GIN and Campbell) concluded, with the agreement of our local host - CEBHC-KT and Masaryk University, that the most appropriate decision is to postpone the Summit until 9 – 13 September 2024. As global leaders in evidence-informed healthcare, the partners take very seriously our responsibility and duty of care to our communities in the face of continuing risks.

However, we are committed to working together, along with additional organizations, to present the third Annual World EBHC Day on 20 October, 2022. This is a global initiative that raises awareness of the need for better evidence to inform healthcare policy, practice and decision making to improve health outcomes globally.

This second postponement of the second Global Evidence Summit is disappointing news for all of us and we would like to thank the vast number of people, including our local hosts, who have been working hard on preparations over the past year. We are in no doubt that we will be able to build successfully on the work accomplished so far to ensure that when GES 2 does go ahead in September 2024 in Prague it will be everything we anticipated: a world-class scientific event and a memorable gathering of the evidence-based healthcare community. 

We thank you for your ongoing support and commitment to the Global Evidence Summit and will look forward to meeting again for this unique event in 2024. 

Recent developments have shown the world can be volatile and unpredictable, requiring us to remain vigilant and responsive – collaborations such as this are even more important.   We hope that you all remain safe and well during these extraordinary times. 

Miloslav Klugar
Director, CEBHC-KT (Czech Cochrane, JBI and GRADE centres), Chair of the GES Scientific Committee

Judith Brodie
Interim CEO, Cochrane

Zoe Jordan
Executive Director, JBI

Elaine Harrow
CEO, Guidelines International Network

Vivian Welch,
Interim CEO, The Campbell Collaboration

Wednesday, May 4, 2022
Muriah Umoquit

Global rollout of rapid molecular tests for tuberculosis over the last 12 years: Cochrane Review summarizes research on recipient and provider views

3 years 7 months ago

A potential game-changer in the tuberculosis epidemic was how the tuberculosis community viewed rapid molecular tests for tuberculosis and tuberculosis drug resistance. This was 12 years ago, with the launch of Xpert MTB/RIF, which gives results in less than two hours, simultaneously diagnosing tuberculosis and testing if the bacteria have rifampicin resistance, a type of drug-resistant tuberculosis. Multidrug-resistant tuberculosis is caused by resistance to at least both rifampicin and isoniazid, the two most effective first-line drugs used to treat tuberculosis. 

Yet, diagnostic tests only have an impact on health if they are put to use in a correct and timely manner. To ensure diagnostics are accessible and utilized, we need to understand the views of recipients and providers who have used these tests, and a new qualitative evidence synthesis review published by the Cochrane Infectious Diseases Group (CIDG) pulls together all relevant research to date on Xpert MTB/RIF and similar tests. The authors also wanted to understand the implications of the review findings on effective implementation and health equity.

Rapid molecular tests have been shown to be accurate in diagnosing tuberculosis and rifampicin resistance and are recommended by the World Health Organization as the initial test in people with presumptive tuberculosis, replacing sputum microscopy, a test from the 19th century. These tests have many benefits, including the fact that they do not require well-equipped laboratories and skilled personnel, and can be carried out in community health settings, nearer to where people live. This is particularly relevant in low- and middle-income countries, settings with a high burden of tuberculosis.

Examining the evidence from 32 included studies, the review author team identified aspects of these tests that users valued  most and challenges to realizing those values.  People with tuberculosis valued an accurate diagnosis (knowing what is wrong with me), avoiding delays, and keeping diagnostic-associated cost low. Similarly, healthcare providers valued test accuracy and confidence in results (which helps in starting treatment), rapid results, and keeping cost to people seeking a diagnosis low. In addition, providers valued diversity of sample types (for example, gastric aspirate specimens and stool in children) and ability to detect drug resistance early. Laboratory professionals appreciated the improved ease of use compared to microscopy and increased staff satisfaction.

Reported challenges included reluctance to test for tuberculosis owing to stigma or cost concerns; health system inefficiencies such as poor quality of specimens, difficulty in transporting specimens, lack of sufficient staff or equipment, increased workload for providers, inefficiencies in integrating the test into clinic routines and clinicians relying too much on the test result at expense of their own experience with diagnosing tuberculosis; as well as implementation processes hampered by insufficient  data about real-life situations, lack of inclusion of all relevant stakeholders (local decision-makers, providers or people seeking a diagnosis), and conflicts of interest between donors and people implementing the tests.

Nora Engel, lead author of the review, explains: 

“The findings reveal a fundamental paradox between supporting technological innovations but not in parallel investing in health system infrastructure strengthening. The view that these low-complexity diagnostics are a solution to overcome deficiencies in laboratory infrastructure and lack of skilled professional is misleading. Implementation of new diagnostic technologies, like those considered in this review, will need to tackle the challenges identified in this review including weak infrastructure and systems, and insufficient data on ground level realities prior and during implementation, as well as problems of conflicts of interest in order to ensure quality care and equitable use of resources.”

The review authors called for future research to examine the implications of repurposing diagnostic infrastructure and equipment for COVID-19 and the issue of competition for diagnostic resources more generally.

Engel N, Ochodo EA, Karanja PW, Schmidt BM, Janssen R, Steingart KR, et al. Rapid molecular tests for tuberculosis and tuberculosis drug resistance: a qualitative evidence synthesis. Cochrane Database of Systematic Reviews 2022, Issue 4. Art. No.: CD014877. DOI: 10.1002/14651858.CD014877.pub2

This news article was first published on the LSTM website.

Monday, May 2, 2022
Muriah Umoquit

Cochrane releases RevMan Web software for non-Cochrane systematic reviews

3 years 7 months ago

Cochrane is delighted to announce the availability for the first time of RevMan Web, its popular, web-based systematic-review production software, to the wider community beyond Cochrane – to support evidence synthesis development and evidence-based medicine education. Cochrane expects interest in use of the tool from those in guideline and Health Technology Assessment organisations, universities and medical schools, and many other research sectors.

RevMan Web facilitates the creation of meta-analyses, forest plots, risk-of-bias tables, and other systematic review elements. It is acknowledged to be easy-to-use – and is also widely used in learning or training about systematic review production.

Cochrane is making RevMan Web available for use by institutions or individuals for their own systematic review development work. The product is presented on a Software-as-a-Service basis: Cochrane offers a hosted service, comprising the software and cloud storage of all review data uploaded. 

Charlotte Pestridge, Cochrane’s Director of Publishing and Technology, says this is a hugely exciting opportunity:

“Making RevMan Web more widely available is an important element in Cochrane’s contribution to healthcare research and our mission to deliver evidence-informed policy and practice through the production of systematic reviews. It is important for Cochrane to be able to support the production of high-quality reviews using Cochrane standards and methodologies. Many review-producing organisations, including key Cochrane stakeholders, already use RevMan.”

 RevMan Web is now available by subscription to government and commercial organizations. Availability for academic institutions and individual subscribers is expected to come on stream before the end of 2022. Free access will be available in Reseach4Life Hinari low and middle-income countries.

To find out more:

Wednesday, June 1, 2022
Muriah Umoquit

Cochrane seeks Evidence Synthesis Development Editor - UK

3 years 7 months ago

Specifications: Permanent
Salary: circa £45,000 per annum
Location: UK
Application Closing Date:  5 June 2022

The Evidence Production and Methods Directorate in Cochrane is made up of three departments that are responsible for the efficient and timely production of high-quality Cochrane Reviews addressing research questions that are most important to decision makers.

As Evidence Synthesis Development Editor in the Methods and Evidence Synthesis Development team, you will be working on new and updated Cochrane Reviews prior to their completion and submission for editorial process. The role-holder will need to ensure that protocols and new or updated reviews will meet Cochrane’s quality standards.

The role-holder will need to be able to recognise when to refer methodological questions to colleagues with specialist methods expertise in the Methods Support Unit or Cochrane Methods Groups for further advice, especially around the assessment of bias and statistical methods.

Cochrane is a global independent network of health practitioners, researchers, patient advocates and others, responding to the challenge of making the vast amounts of evidence generated through research useful for informing decisions about health. We do this by identifying, appraising and synthesizing individual research findings to produce the best available evidence on what can work, what might harm and where more research is needed.

How to apply

  • For further information on the role and how to apply, please click here
  • The deadline to receive your application is by 5 June 2022. 
  • The supporting statement should indicate why you are applying for the post, and how far you meet the requirements, using specific examples.
  • Note that we will assess applications as they are received, and therefore may fill the post before the deadline.
  • Read our Recruitment Privacy Statement 

Tuesday, May 24, 2022 Category: Jobs
Lydia Parsonson

Pružanje skrbi i strategije samostalne skrbi djece s epilepsijom

3 years 7 months ago
Pružanje skrbi i strategije samostalne skrbi djece s epilepsijom Dosadašnje spoznaje Epilepsija je poremećaj koji utječe na živčani sustav djece i odraslih. Do epileptičkih napadaja dolazi zbog pretjerane i abnormalne aktivnosti mozga, a učestalost napadaja ne može se predvidjeti. Lijekovi protiv napadaja i drugi oblici liječenja mogu spriječiti većinu napadaja, ali epilepsija može uzrokovati probleme u društvu, školi ili na radnome mjestu te time otežava samostalan život. Osobe koje pate od napadaja često imaju fizičke probleme (npr. prijelome, modrice i nešto veći rizik od iznenadne...

Oblozi uz negativni tlak za zatvorene kirurške rane

3 years 7 months ago
Oblozi uz negativni tlak za zatvorene kirurške rane Ključne poruke Terapija rane negativnim tlakom (TRNT) vjerojatno smanjuje više infekcija kirurških rana nego standardni oblozi u osoba sa zatvorenim ranama nakon operacije. TRNT vjerojatno ne utječe na broj osoba kod kojih je došlo do ponovnog otvaranja rane (dehiscencije) nakon operacije i može imati neznatan ili nikakav utjecaj na broj umrlih. TRNT može povećati broj osoba s plikovima na koži nakon operacije, ali može imati neznatan ili nikakav utjecaj na druge ishode. Isplativost TRNT-a i pouzdanost ovih zaključaka ovisi o vrsti...

Korištenje probiotika za sprječavanje Hirschsprungova enterokolitisa

3 years 7 months ago
Korištenje probiotika za sprječavanje Hirschsprungova enterokolitisa Istraživačko pitanje Koje su prednosti i rizici korištenja probiotika za sprječavanje Hirschsprungova enterokolitisa (engl. Hirschsprung-associated enterocolitis, HAEC)? Ključne poruke Uspoređeni su randomizirani kontrolirani pokusi (RCT) koji su koristili probiotike i placebo (ili bilo koje drugo liječenje u kojem se ne koriste probiotici) za prevenciju Hirschsprungova enterokolitisa. Trenutno nema dovoljno dokaza za procjenu učinkovitosti ili sigurnosti probiotika za prevenciju Hirschsprungova enterokolitisa. Što je...

Cochrane launches report summarising what we have heard from our diversity and inclusion listening and learning exercise

3 years 7 months ago

Cochrane wants to welcome people, no matter who they are or where they live. The more varied perspectives we have, the better we can provide evidence to help inform health and healthcare decisions.

In October 2021, we launched our listening and learning exercise that aimed to gather data, views and experiences regarding diversity and inclusion in Cochrane. Between October and January we heard from over 1,300 people and we are pleased to publish the findings in this new report.

We encourage everyone to read this report and we have made a summary of the report available in multiple languages to increase accessibility.

Chris Champion, Head of People Services, says

“Cochrane is a worldwide organisation that aspires to be diverse and inclusive. We want everyone to be able to participate in Cochrane, regardless of who they are and where they come from. This matters to Cochrane, because if we are more inclusive, we will be able to provide better and more relevant evidence to our users who are at the heart of our vision.”


Thank you to everyone who contributed to this important process. It is clear that we can do a lot more to be a diverse and inclusive organisation, so the important work starts now as we take action in response to these findings.

Monday, April 25, 2022
Muriah Umoquit

Operacija na oba oka istog dana ili na zasebne dane: što je bolje za liječenje katarakte na oba oka?

3 years 7 months ago
Operacija na oba oka istog dana ili na zasebne dane: što je bolje za liječenje katarakte na oba oka? Ključne poruke - trenutni dokazi pokazuju kako postoje neznatne razlike između operacija očiju istog dana (engl. immediate sequential bilateral surgery, ISBCS) ili na zasebne dane (engl. delayed sequential bilateral surgery, DSBCS) za sljedeće kliničke ishode: očne infekcije (endoftalmitis, ozbiljna i opasna za vid, ali rijetka komplikacija), korekcijske naočale nakon operacije (refrakcija), komplikacije vida s korekcijskim naočalama (prema potrebi) te za ishode koje opisuju pacijenti (engl....

Psihoterapijsko liječenje depresije i anksioznosti u pacijenata s demencijom i blagim kognitivnim oštećenjem

3 years 7 months ago
Psihoterapijsko liječenje depresije i anksioznosti u pacijenata s demencijom i blagim kognitivnim oštećenjem Ključni rezultati - Psihoterapija u obliku kognitivno-bihevioralne terapije (koja je usmjerena na promjenu mišljenja i ponašanja) vjerojatno ima mali pozitivan učinak na depresiju, kvalitetu života i svakodnevne aktivnosti ljudi s demencijom ili blagim kognitivnim oštećenjem. - Nema dovoljno dokaza za donošenje zaključaka o učinkovitosti psihoterapije u liječenju anksioznih poremećaja kod osoba s demencijom ili blagim kognitivnom oštećenjem. - Potrebno je više dokaza o različitim...

Obogaćivanje soli željezom i jodom ili samim jodom za poboljšanje statusa željeza i joda

3 years 7 months ago
Obogaćivanje soli željezom i jodom ili samim jodom za poboljšanje statusa željeza i joda Ključne poruke Dvostruko obogaćena sol (sol obogaćena željezom i jodom) u usporedbi sa samo jodiranom soli može poboljšati vrijednosti povezane s konzumacijom željeza i joda, poput koncentracije hemoglobina (tvari koja daje boju crvenim krvnim stanicama) i zaliha željeza u organizmu. No to može smanjiti koncentraciju joda u mokraći i imati slab ili nikakav utjecaj na koncentraciju feritina (proteina za pohranu zalihe željeza) i receptora transferina (proteina koji utječu na unos željeza). U usporedbi s...

Cochrane Infectious Diseases Group seeks Research Associate - Liverpool, UK

3 years 7 months ago

Salary: £35,326 per annum
Contract type: Full-time Fixed term until March 2024
Closing date: 15 May 2022

LSTM’s Centre for Evidence Synthesis in Global Health runs the “Research, Evidence and Development Initiative” (READ-It) and contains the Cochrane Infectious Diseases Group (CIDG). The CIDG was established in 1995. They are world leaders in evidence synthesis related to public health in the tropics. They have a wide portfolio of Cochrane reviews in malaria and neglected tropical diseases, amongst other topics.

Teams are already in place for some of the reviews and they have experienced technical specialists in all areas. The successful candidate will assure the delivery of a portfolio of high-quality Cochrane reviews according to LSTM’s strategic plan.   You will be part of the READ-It Management Team and assure the delivery of the CIDG Partners deliverables.

Key Responsibilities are (but not limited to):

  • Provide editorial feedback to the Managing Editor throughout the review life cycle
  • To stay up to date with Cochrane methods, standards, and procedures and ensure reviews are in compliance
  • Work with the CIDG team in ensuring efficient and effective editorial processes are in place
  • Assessing technical and academic aspects of reports from READ-It Partners, and the draft READ-It annual reports to funders
  • Actively manage review delivery and report and discuss progress of Liverpool associated outputs with the READ-It Management Team
  • Participate in READ-It Management Team meetings, Partner meetings, and Advisory Group meetings
  • Liaise with READ-It Liverpool staff and the Head of the Department of Clinical Sciences (DoCS) to assure appropriate line management including the performance conversation process
  • Assure delivery of the CIDG strategic plan in relation to reviews by supporting teams and helping overcome review production obstacles
  • Work with stakeholders, editors, and the CRG strategic advisory group in taking on new topics and teams in line with priorities, stakeholder needs and CIDG capacity
  • Deliver seminars for Diploma and Master students
  • Actively contribute to submissions for grant funding

The Candidate will ideally be:

Candidates must be experienced in Cochrane systematic reviews to work in our Liverpool team and with our global partners to help assure the delivery of the CIDG strategic plan. 

  • Hold a Postgraduate professional qualification, such as the Diploma of Tropical Medicine, or health-related Masters’ degree
  • Have knowledge of systematic reviews and RCT trial basics
  • Have knowledge and an interest in LMICs and infectious disease problems
  • Understand qualitative and quantitative research methods
  • Be experienced in the critical appraisal of medical literature at postgraduate level

For a confidential discussion about this role, please contact Paul Garner at: Paul.Garner@lstmed.ac.uk(link sends e-mail)

Additional benefits of joining LSTM:

  • 30 days annual leave, plus bank holidays, plus Christmas closure days
  • Generous occupational pension schemes
  • Government backed “cycle to work” scheme.
  • Affiliated, discounted staff membership to the University of Liverpool Sports Centre
  • Plus, a host of additional family friendly policies

Closing Date: 15th May 2022 
More information and to apply: https://www.lstmed.ac.uk/research-associate-66636

Tuesday, April 19, 2022 Category: Jobs
Muriah Umoquit

Pomaže li liječenje bolesti desni u kontroli razine šećera u krvi osobama sa šećernom bolešću?

3 years 8 months ago
Pomaže li liječenje bolesti desni u kontroli razine šećera u krvi osobama sa šećernom bolešću? Cilj sustavnog pregleda Glavno pitanje ovog Cochraneovog sustavnog pregleda: koliko je učinkovito liječenje desni u kontroliranju razine šećera u krvi (kontrola glikemije) u osoba s dijabetesom u odnosu na nikakvo aktivno liječenje ili uobičajenu skrb? Dosadašnje spoznaje Cilj liječenja parodontitisa je smanjenje oticanja i infekcije te stabilizacija stanja zubnog mesa i potporne kosti. Razina šećera u krvi u osoba s dijabetesom je previsoka pa je ključni problem održavanje razine šećera u krvi pod...

Može li usredotočena svjesnost pomoći ljudima da prestanu pušiti?

3 years 8 months ago
Može li usredotočena svjesnost pomoći ljudima da prestanu pušiti? Ključne poruke - Trenutno nema jasnih dokaza da liječenje temeljeno na usredotočenoj svjesnosti pomaže ljudima da prestanu pušiti ili da poboljšava njihovo mentalno zdravlje i dobrostanje. - Međutim, naše je povjerenje u dokaze vrlo nisko, a daljnji dokazi vjerojatno će promijeniti naše zaključke. Što je usredotočena svjesnost (engl. mindfulness)? Usredotočena svjesnost uključuje usmjeravanje pažnje na svoje misli i osjećaje te njihovo promatranje bez osuđivanja dok nastaju i prolaze. Vjeruje se da usredotočena svjesnost...

Cochrane seeks Editorial Assistant - Flexible location, remote

3 years 8 months ago

Specifications: Full Time 1 year Fixed Term contract/Consultancy contract
Salary:  £25,540 per annum
Location: Flexible (remote)
Application Closing Date: 22 April 2022 (midnight GMT)

Cochrane has established a Central Editorial Service to support the efficient and timely publication of high-quality systematic reviews in the Cochrane Library. The reviews that are published through the Central Editorial Service address some of the research questions considered to be the most important to decision makers. The Central Editorial Service is also instrumental in running a pilot aiming to improve editorial independence and efficiency within Cochrane. The Editorial Assistant role will play a key role in operationalising this pilot.

The Editorial Assistant will perform editorial tasks to support the smooth running of the Editorial Service. Tasks will include, but are not limited to: performing checks on manuscripts on submission and before publication; supporting the peer-review process including inviting peer reviewers and tracking progress; assisting authors and peer reviewers to use Cochrane’s Editorial Management System; running editorial reports for the Editorial Service Executive Editor; arranging and preparing documents for editorial meetings; and supporting the Head of Editorial in projects aimed at improving or developing editorial systems and processes.
Cochrane is a global independent network of health practitioners, researchers, patient advocates and others, responding to the challenge of making the vast amounts of evidence generated through research useful for informing decisions about health. We do this by identifying, appraising and synthesizing individual research findings to produce the best available evidence on what can work, what might harm and where more research is needed.


For further information on the role and how to apply, please click here.  The supporting statement should indicate why you are applying for the post, and how far you meet the requirements, using specific examples. Note that we will assess applications as they are received, and therefore may fill the post before the deadline.
Deadline for applications: 22 April 2022 (midnight GMT).

Friday, April 8, 2022 Category: Jobs
Lydia Parsonson

Featured review: Control interventions in randomized trials among people with mental health disorders

3 years 8 months ago

New Cochrane Review: Control interventions in randomised trials for people with a mental health disorder

KEY MESSAGES

  • Researchers use many different control interventions in randomized trials on treatments for patients with mental health disorders, but there is little consensus on how to report and adequately design these controls. This practice has widespread consequences for the evidence base underpinning psychiatric treatments
  • The choice, design and reporting of a control intervention is just as important as the experimental treatment in a randomized trial with psychiatric patients. This is not reflected in most randomized trials with mental health patients, as control interventions are often poorly reported upon and lack methodological rigor
  • Some psychiatric treatments may be recommended based on just having compared the treatment with a waitlist or no-treatment control in a randomized trial, which may give a misleading picture of how effective the treatment is

Erlend Faltinsen, lead author,  commented, "There is a need to develop methodological guidelines on how to design and report upon control interventions in randomized trials on psychiatric treatments, as trialists working in the field of mental health do not have a solid evidence-based framework to draw from on this issue."

Why was this review conducted?
The review investigates the beneficial and harmful effects between different control interventions in randomized trials with mental health patients. We wanted to investigate how control interventions differ from each other and to lay the empirical groundwork to develop methodological guidelines on reporting, and the design of control interventions in psychiatric randomized trials.

What did the authors do?
The authors conducted a Cochrane systematic review and meta-analysis to assess the benefits and harms between placebo, usual care (or treatment as usual) and waitlist controls versus receiving no treatment.  In that way they assessed how effective and harmful different control interventions in psychiatric randomized trials are.

What did they find?

  • 96 randomized trials were included and the trials involved 15 different types of mental health disorders
  • When combining three different types of placebos, the beneficial effects compared with no-treatment or wait-list controls was small to moderate
  • There was no significant difference between usual care controls and wait-list or no-treatment on benefits. The same was true for waitlist versus no-treatment controls
  • Psychological placebos (non-active controls used mostly in psychotherapy research) showed moderate effects compared with no treatment whereas placebos used for physical treatments like surgery showed a small effect. We found no significant effects of pharmacological placebos versus no treatment
  • There was little data on harms between the control interventions and the findings on harms were insignificant
  • The control interventions were mostly poorly reported upon and there was little rationale for why a given control was used in most reports

What are the limitations of the evidence?
The certainty of the evidence was rated low to very low, and the risk of bias was rated high in all studies. The authors mostly included randomized trials with three intervention arms to compare two controls, which causes issues with blinding of participants and trial personnel. This limitation was due to the methodological objective of the review and may be viewed as part of the review itself rather than a flaw in the evidence-base. Many of the studies were small, however, leading to risk of small-study effects, which limits the evidence.

What gaps did the authors identify?
There is a need to develop methodological guidelines on control interventions in psychiatric randomized trials, as trialists working in the field of mental health do not have a solid evidence-based framework to work from when choosing and reporting upon controls



What important related questions were not addressed in this review?
The review did not compare usual care with placebo interventions, which would have been relevant. It did not quantify the level of reporting issues and rationale for choosing a control in a psychiatric randomized trial, which also would have been relevant.

Who will find this review most relevant?
Psychiatric researchers and especially those who conduct randomized trials will find the review relevant for their research work. It may also appeal to trialists in general and methodologists.

How up to date is this review?
The search was conducted in March 2018. The researchers were not able to screen records after this date, since the search process was very large and extracting data was exceptionally time-consuming.

Friday, April 8, 2022
Lydia Parsonson