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OpenTrials
Completed

NCT Number: NCT01759485

Vitamin D for Schizophrenia

Background: Despite improvements in medications, treatment delivery and rehabilitation, schizophrenia outcomes remain suboptimal. There are a proportion of 30-40% treatment-resistant schizophrenia patients. Multiple lines of evidence suggest that vitamin D is a neuro-active steroid that acts on brain development, leading to alterations in brain neurochemistry and adult brain function. Early deficiencies have been linked with neuropsychiatric disorders, such as schizophrenia, and adult deficiencies have been associated with adverse brain outcomes, including Parkinson's disease, Alzheimer's disease, depression and cognitive decline. Ecological studies support a potential role for vitamin D in schizophrenia. These data include studies that have explored the association between schizophrenia and winter/spring birth and also the apparent increased incidence and prevalence of schizophrenia at higher latitudes. Objective: To evaluate the effect of vitamin-D supplementation on the mental state of clozapine-treated chronic schizophrenia patients, and the relation of disease severity to serum vitamin D levels. Methods: the investigators will use a prospective, interventional, longitudinal, double blinded, placebo-controlled, randomized design. The investigators will recruit 50 clozapine-treated chronic schizophrenia patients, with low level of serum vitamin-D, that will be randomly assigned (1:1 ratio) to receive either weekly oral drops of vitamin D (Cholecalciferol) or oral drops of placebo for 8 weeks follow-up. Repeated assessments will include: clinical severity scales (PANSS, CGI), side effects (SAS, BARS, clozapine side effects), cognitive (MoCA), metabolic parameters and laboratory data. Patients who were assigned to placebo will be supplemented with vitamin D after the 8 weeks period, and then will be assessed again with the same protocol of vitamin D treated patients. All participants will be assessed again after 24 weeks after vitamin D initiation. Analysis: the investigators will use on-way ANOVA with repeated measures for comparison of vitamin D and control groups. The investigators will apply intention to treat and LOCF.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Geha Mental Health Center

Petah Tikva, 45000, Israel

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and females
  • Age 18-65 years
  • Diagnosis of schizophrenia according to DSM-IV-TR criteria, as confirmed by two senior psychiatrists
  • Total PANSS score > 70
  • CGI-S > 3
  • Clozapine treatment for at least 18 weeks
  • Vitamin D deficiency: plasma 25-OH-Vitamin D <75 nmol/L (20-30 ng/mL)
  • Able to consume oral drops of vitamin-D
  • Able to sign informed consent

Exclusion criteria

  • Mental retardation
  • Organic brain disease
  • Known parathyroid disorder
  • Inborn/acquired vitamin D metabolism disorders
  • Patients already treated with vitamin D supplementation

Treatment and study plan

Vitamin D3

Drug

once weekly oral drops preparation at a daily dose of 2000 IU X 7 = 14,000 IU per week (about 60 drops each week).

Other names: Cholecalciferol

Placebo

Drug

Primary outcomes

  1. Change in Positive and Negative Syndrome Scale total score

    Time frame: Baseline to 8 weeks

Secondary outcomes

  1. Change in the MoCA Cognitive composite score

    Time frame: Baseline to 8 weeks

Other outcomes

  1. Change in Positive and Negative Syndrome Scale sub-scores

    Time frame: Baseline to 8 weeks

Sponsors and collaborators

Lead sponsor

Geha Mental Health Center

Other

Registry information

Official study title

Vitamin D Supplementation as Adjunct to Clozapine-treated Chronic Schizophrenia Patients

Important dates

Study start
2014
Primary completion
2016
Study completion
2017
First posted
Jan 3, 2013
Registry last updated
Apr 13, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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