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Vitamin D for Schizophrenia

Primary Purpose

Clozapine Resistant Schizophrenia

Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Vitamin D3
placebo
Sponsored by
Geha Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Clozapine Resistant Schizophrenia focused on measuring Clozapine, Schizophrenia, Vitamin-D, Treatment-resistant

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

  1. Mental retardation
  2. Organic brain disease
  3. Known parathyroid disorder
  4. Inborn/acquired vitamin D metabolism disorders
  5. Patients already treated with vitamin D supplementation

Sites / Locations

  • Geha Mental Health Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Vitamin D

Placebo

Arm Description

Supplementation of Vitamin D as add-on to the regular anti-psychotic treatment

Placebo as oral drops once weekly as add-on to the regular anti-psychotic treatment

Outcomes

Primary Outcome Measures

Change in Positive and Negative Syndrome Scale total score

Secondary Outcome Measures

Change in the MoCA Cognitive composite score

Full Information

First Posted
December 4, 2012
Last Updated
April 12, 2017
Sponsor
Geha Mental Health Center
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1. Study Identification

Unique Protocol Identification Number
NCT01759485
Brief Title
Vitamin D for Schizophrenia
Official Title
Vitamin D Supplementation as Adjunct to Clozapine-treated Chronic Schizophrenia Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
May 2014 (Actual)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
February 28, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Geha Mental Health Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clozapine Resistant Schizophrenia
Keywords
Clozapine, Schizophrenia, Vitamin-D, Treatment-resistant

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D
Arm Type
Active Comparator
Arm Description
Supplementation of Vitamin D as add-on to the regular anti-psychotic treatment
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo as oral drops once weekly as add-on to the regular anti-psychotic treatment
Intervention Type
Drug
Intervention Name(s)
Vitamin D3
Other Intervention Name(s)
Cholecalciferol
Intervention Description
once weekly oral drops preparation at a daily dose of 2000 IU X 7 = 14,000 IU per week (about 60 drops each week).
Intervention Type
Drug
Intervention Name(s)
placebo
Primary Outcome Measure Information:
Title
Change in Positive and Negative Syndrome Scale total score
Time Frame
Baseline to 8 weeks
Secondary Outcome Measure Information:
Title
Change in the MoCA Cognitive composite score
Time Frame
Baseline to 8 weeks
Other Pre-specified Outcome Measures:
Title
Change in Positive and Negative Syndrome Scale sub-scores
Time Frame
Baseline to 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Geha Mental Health Center
City
Petach-Tikva
ZIP/Postal Code
45000
Country
Israel

12. IPD Sharing Statement

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Vitamin D for Schizophrenia

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