Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2811
Title: The efficacy of sodium benzoate as an adjunctive treatment in early psychosis - CADENCE-BZ: Study protocol for a randomized controlled trial
Authors: Group, C. W.
Scott, J.
Baker, A.
Dark, F.
Foley, S.
Gordon, A.
Hatherill, S.
Stathis, S.
Saha, S.
Bruxner, G.
Beckman, M.
Richardson, D.
Berk, M.
Dean, O.
McGrath, J.
Ryan, A.
Issue Date: 2017
Source: 18, (1), 2017
Journal: Trials
Abstract: Background: Psychotic disorders affect up to 3% of the population and are often chronic and disabling. Innovation in the pharmacological treatment of psychosis has remained stagnant in recent decades. In order to improve outcomes for those with psychotic disorders, we present a protocol for the trial of a common food preservative, sodium benzoate, as an adjunctive treatment in early psychosis. Methods: Persons experiencing early psychosis (n=160) will be recruited through hospitals and community mental health services in Queensland, Australia. Patients will be randomized to receive either 12-week treatment with 1000mg (500mg twice daily (BD)) sodium benzoate or placebo. Patients will undergo fortnightly outcome assessments, in addition to weekly ongoing capacity to consent, drug compliance and safety assessments. The primary outcome measure is the Positive and Negative Syndrome Scale (PANSS) total score. Secondary outcomes are Global Assessment of Function (GAF), Assessment of Quality of Life Scale (AQOL), the Activity and Participation Questionnaire (APQ6), International Physical Activity Questionnaires (IPAQ), Simple Physical Activity Questionnaire (SIMPAQ), Physical Activity Questionnaire, Clinical Global Impression (CGI), Hamilton Depression rating Scale-17 items (HDRS), Opiate Treatment Index (OTI) and the Patients' Global Impression of Improvement (PGI-I). As a tertiary objective, changes from baseline to endpoint in to serum markers related to D-alanine, L-alanine, D-serine, L-serine, glycine and glutamate will be investigated. Discussion: Consumers and clinicians are keen to help develop better treatments for those with psychosis. This study, part of the wider Cadence clinical trials platform will examine if a safe and accessible food preservative can help optimize outcomes in those with psychosis. Trial Registration: Australian New Zealand Clinical Trials registry (ANZCTR), ACTRN12615000187549. Registered on 26 February 2015.L6156143022017-05-02
2017-05-09
DOI: 10.1186/s13063-017-1908-5
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L615614302&from=exporthttp://dx.doi.org/10.1186/s13063-017-1908-5 |
Keywords: mental health service;methodology;multicenter study;Opiate Treatment Index;outcome assessment;parallel design;patient compliance;Patients Global Impression of Improvement;Positive and Negative Syndrome Scale;psychosis;quality of life assessment;randomized controlled trial;sample size;Simple Physical Activity Questionnaire;treatment outcome;unspecified side effect;treatment duration;12615000187549benzoic acid;dextro alanine;dextro serine;glutamic acid;glycine;placebo;serine;Activity and Participation Questionnaire;add on therapy;adjuvant therapy;adult;article;Assessment of Quality of Life Scale;Australia;behavior assessment;Clinical Global Impression scale;controlled study;double blind procedure;drug efficacy;drug safety;female;general mental disease assessment;Global Assessment of Functioning;Hamilton Depression Rating Scale;human;international physical activity questionnaire;major clinical study;male
Type: Article
Appears in Sites:Children's Health Queensland Publications

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