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      Vitamin D supplementation compared to placebo in people with First Episode psychosis - Neuroprotection Design (DFEND): a protocol for a randomised, double-blind, placebo-controlled, parallel-group trial

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          Abstract

          Background

          People experiencing their first episode of psychosis are often deficient in vitamin D. Observational studies have reported an association between low vitamin D concentrations and poorer subsequent health outcomes in psychosis. A vitamin D deficiency in neonates and children has been linked to a later increased risk of schizophrenia and psychotic-like experiences. This trial aims to examine the effect of high-dose vitamin D supplementation on outcomes in early psychosis. We hypothesise that vitamin D supplementation will be associated with better mental health outcomes.

          Methods/design

          The DFEND study is a multicentre double-blind placebo-controlled parallel-group trial of vitamin D supplementation in people with early psychosis. Patients with an ICD-10 diagnosis of functional psychosis will be randomised in a 1:1 ratio to receive either 120,000 IU/month of vitamin D (cholecalciferol) or a matched placebo for 6 months. The primary outcome is the total Positive and Negative Syndrome Scale (PANSS) score at the 6-month follow-up for all patients. Secondary outcomes include assessment of mood (Calgary Depression Scale), general function (Global Assessment of Functioning), cardiovascular risk (body mass index, waist circumference, C-reactive protein, cholesterol and HbA1c) and vitamin D levels at the 6-month follow-up. Additionally, 3- and 6-month total PANSS scores will be analysed for those with inadequate vitamin D levels at the baseline.

          Discussion

          The DFEND study is the first trial to examine whether vitamin D supplementation in early psychosis is associated with better mental health outcomes. The findings of this study may help to resolve the clinical equipoise regarding the benefits and cost-effectiveness of routine vitamin D supplementation in people with psychosis.

          Trial registration

          ISRCTN, ISRCTN12424842. Registered on 25 February 2015.

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          Most cited references41

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          Global assessment of functioning. A modified scale.

          The modified Global Assessment of Functioning (GAF) scale has more detailed criteria and a more structured scoring system than the original GAF. The two scales were compared for reliability and validity. Raters who had different training levels assigned hospital admission and discharge GAF scores from patient charts. Intraclass correlation coefficients for admission GAF scores were higher for raters who used the modified GAF (0.81), compared with raters who used the original GAF (0.62). Validity studies showed a high correlation (0.80) between the two sets of scores. The modified GAF also correlated well with Zung Depression scores (-0.73). The modified GAF may be particularly useful when interrater reliability needs to be maximum and/or when persons with varying skills and employment backgrounds--and without much GAF training--must rate patients. Because of the increased structure, the modified GAF may also be more resistant to rater bias.
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            A brief mental health outcome scale-reliability and validity of the Global Assessment of Functioning (GAF).

            The Global Assessment of Functioning (GAF) is a quick and simple measure of overall psychological disturbance. However, there is little research on the reliability and validity of this measure in severely mentally ill populations. Multidisciplinary keyworkers assessed 103 patients at monthly intervals over a 6-month period. Overall GAF scores were obtained, with additional separate ratings for symptoms and disability. These were compared with changes in antipsychotic medication and support needs over the same period. Satisfactory reliability was obtained for total GAF score and for symptom and disability measures, in spite of raters having only one brief training session. All GAF scores were associated with current support needs of patients. Symptom and disability scores were associated with changes in antipsychotic medication in the previous month. Only symptom score was associated with increases in antipsychotic medication at time of rating. GAF proved to be a reliable and, within the limits of the indicators used, a valid measure of psychiatric disturbance in our sample of the severely mentally ill. Differences in relationships between the three GAF scores and medication/support needs indicate the usefulness of obtaining all three scores for monitoring levels and type of psychiatric disturbance in this population.
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              Physical health disparities and mental illness: the scandal of premature mortality.

              A 20-year mortality gap for men, and 15 years for women, is still experienced by people with mental illness in high-income countries. The combination of lifestyle risk factors, higher rates of unnatural deaths and poorer physical healthcare contribute to this scandal of premature mortality that contravenes international conventions for the 'right to health.'
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                Author and article information

                Contributors
                fiona.p.gaughran@kcl.ac.uk
                dominic.stringer@kcl.ac.uk
                michael.berk@barwonhealth.org.au
                shubulade.smith@kcl.ac.uk
                David.Taylor@slam.nhs.uk
                eromona.whiskey@slam.nhs.uk
                sabine.landau@kcl.ac.uk
                robin.murray@kcl.ac.uk
                philip.mcguire@kcl.ac.uk
                poonam.sood@kcl.ac.uk
                gabriella.wojewodka@kcl.ac.uk
                simone.ciufolini@kcl.ac.uk
                harriet.jordan@kcl.ac.uk
                jessie.clarke@kcl.ac.uk
                lauren.allen@slam.nhs.uk
                amir.krivoy@kcl.ac.uk
                brendon.stubbs@kcl.ac.uk
                lowephilippa@aol.com
                mauricea@easy.com
                Shanaya.Rathod@southernhealth.nhs.uk
                andrew.boardman@cwp.nhs.ukl
                mudasir.firdosi@swlstg.nhs.uk
                j.mcgrath@uq.edu.au
                Journal
                Trials
                Trials
                Trials
                BioMed Central (London )
                1745-6215
                6 January 2020
                6 January 2020
                2020
                : 21
                : 14
                Affiliations
                [1 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, Department of Psychosis Studies, , King’s College London, Institute of Psychiatry, Psychology and Neuroscience, ; 16 De Crespigny Park, London, SE5 8AF UK
                [2 ]ISNI 0000 0000 9439 0839, GRID grid.37640.36, South London and Maudsley NHS Foundation Trust, ; Denmark Hill, London, SE5 8AZ UK
                [3 ]ISNI 0000 0001 2322 6764, GRID grid.13097.3c, Department of Biostatistics and Health Informatics, , King’s College London, Institute of Psychiatry, Psychology and Neuroscience, ; 16 De Crespigny Park, London, SE5 8AF UK
                [4 ]ISNI 0000 0001 0526 7079, GRID grid.1021.2, Deakin University and Barwon Health, ; Ryrie Street, Geelong, Victoria 3220 Australia
                [5 ]ISNI 0000 0000 9653 8171, GRID grid.499484.c, Carer Expert and Chair of Trustees, Rethink Mental Illness, ; 89 Albert Embankment, London, SE1 7TP UK
                [6 ]London, UK
                [7 ]ISNI 0000 0004 0435 8173, GRID grid.416105.7, Clinical Trials Facility, Research Department, Tom Rudd Unit, , Moorgreen Hospital, ; Southampton, SO3 03J UK
                [8 ]Cheshire & Wirral Partnership NHS Trust, Churton House, Countess of Chester Health Park, Chester, CH2 1BQ UK
                [9 ]ISNI 0000 0001 0304 2669, GRID grid.415553.3, South West London and St George’s Mental Health NHS Trust, Queen Mary’s Hospital, ; Roehampton Lane, London, SW15 5PN UK
                [10 ]ISNI 0000 0004 0606 3563, GRID grid.417162.7, Queensland Centre for Mental Health Research, The Park Centre for Mental Health, ; Wacol, QLD 4076 Australia
                [11 ]ISNI 0000 0000 9320 7537, GRID grid.1003.2, Queensland Brain Institute, University of Queensland, ; Brisbane, QLD 4072 Australia
                [12 ]ISNI 0000 0001 1956 2722, GRID grid.7048.b, National Centre for Register-Based Research, , Aarhus University, ; 8000 Aarhus C, Denmark
                Article
                3758
                10.1186/s13063-019-3758-9
                6945550
                b6bdc52e-0343-4fd1-9f8d-8dee7e948cd7
                © The Author(s). 2020

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 27 March 2019
                : 26 September 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100007123, Stanley Medical Research Institute;
                Award ID: 13T-006
                Award Recipient :
                Categories
                Study Protocol
                Custom metadata
                © The Author(s) 2020

                Medicine
                psychosis,first episode,vitamin d,25ohd,randomised controlled trial,positive and negative syndrome scale,mental health

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