Maintenance Notice

Due to necessary scheduled maintenance, the JMIR Publications website will be unavailable from Wednesday, July 01, 2020 at 8:00 PM to 10:00 PM EST. We apologize in advance for any inconvenience this may cause you.

Who will be affected?

Previously submitted to: JMIR Research Protocols (no longer under consideration since May 25, 2023)

Date Submitted: Jun 28, 2022

Warning: This is an author submission that is not peer-reviewed or edited. Preprints - unless they show as "accepted" - should not be relied on to guide clinical practice or health-related behavior and should not be reported in news media as established information.

Plan D- Vitamin D supplementation in psychotic disorders: a placebo controlled randomized trial

  • Mari Nerhus; 
  • Ingrid Melle; 
  • Ketil Hanssen-Bauer; 
  • Thomas D. Bjella; 
  • Ole A. Andreassen; 
  • Nils-Eiel Steen; 
  • Trine Vik Lagerberg

ABSTRACT

Background:

Cognitive impairments and negative symptoms in schizophrenia are associated with poor outcome, and may have common underlying mechanisms, such as psychomotor retardation. Vitamin D is a neuroactive component associated to both cognitive impairments and negative symptoms. The aim of the study is to evaluate the treatment effect of vitamin D supplementation compared to placebo on measures of psychomotor retardation.

Objective:

The primary objective is to investigate whether vitamin D supplementation is superior to placebo in improving processing speed. The secondary objectives are to investigate whether vitamin D supplementation is superior to placebo in improving negative symptoms, social and physical activity.

Methods:

Study design: Randomized placebo-controlled double blind trial. Study population: Men and women, aged 18-65 years, diagnosed with a schizophrenia spectrum disorder, in treatment for their disorder at the Division of Mental Health Services at Akershus University Hospital, and with baseline Vitamin D levels below 75 nmol/l. Intervention: Participants will be randomized 1:1 to either vitamin D3 (50µg capsules) or placebo daily for 12 weeks. The medical product or placebo will be given in addition to treatment as usual. Study measures: Cognitive tests for processing speed, symptom assessments for negative symptoms and blood sampling for vitamin D analyses will be performed at baseline and after 12 weeks intervention. During the 12 week intervention period the participants will use a smart phone application (MinDag) for daily self-report of occupational, social- and physical activity, and biweekly self-report of negative symptoms. Study participants will also wear an actigraph (MotionWatch 8 actigraph from CamNtech) for continuous registration of physical activity.

Results:

The study is currently recruiting. Primary outcome is change in cognitive performance on the symbol coding test from the Brief assessment of Cognition in Schizophrenia (BACS). Secondary outcomes are change in negative symptoms from the clinician rated Brief negative symptom scale (BNSS), and change in self-reported negative symptoms from the scale Self-assessment of Negative Symptoms (SNS). Secondary outcomes also include change in self-reported social activities from the MinDag app and change in actigraph registered physical activity.

Conclusions:

The results from the study will indicate whether vitamin D supplementation could represent a beneficial treatment strategy for impaired processing speed and related symptoms in schizophrenia. Clinical Trial: ClinicalTrials.gov identifier NCT05211635.


 Citation

Please cite as:

Nerhus M, Melle I, Hanssen-Bauer K, Bjella TD, Andreassen OA, Steen NE, Lagerberg TV

Plan D- Vitamin D supplementation in psychotic disorders: a placebo controlled randomized trial

JMIR Preprints. 28/06/2022:40442

DOI: 10.2196/preprints.40442

URL: https://preprints.jmir.org/preprint/40442

Download PDF


Request queued. Please wait while the file is being generated. It may take some time.

© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.