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NCT07579078Enrolling by invitation

Effect of Vitamin D Supplementation on Brain Waves in Female Major Depressive Disorder Patients With Hypovitaminosis D

Effect of Vitamin D Supplementation on Brain Waves in Female Major Depressive Disorder Patients With Hypovitaminosis D : A Quantitative Electroencephalogram Analysis

Source: ClinicalTrials.gov · Last updated 12 May 2026

Brief summary (registry, in English)

Major Depressive Disorder (MDD) is a common mood disorder characterized by persistent sadness, loss of interest and cognitive impairment. Emerging evidence suggests that vitamin D may exert neuroprotective and mood-regulating effects by influencing serotonin synthesis, modulating inflammation and supporting neuronal function. Vitamin D deficiency is frequently observed in MDD patients and has been linked to greater symptom severity and poorer treatment outcomes. Quantitative electroencephalography (QEEG) is a non-invasive tool for assessing brain electrical activity. Alterations in QEEG pattern such as increased theta and reduced alpha power have been reported in patients with MDD , reflecting disrupted cortical processing and emotional regulation. Although interest in the role of vitamin D in mental health is increasing, the direct effect of vitamin D supplementation on QEEG parameters in MDD patients with hypovitaminosis D is not well explored. This study aims to evaluate whether vitamin D supplementation can modulate brain wave activity in female patients with MDD and hypovitaminosis D. Therefore providing insight into its neurophysiological and therapeutic significance.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
34 (estimated)
First submitted
30 Apr 2026
Start date
25 Apr 2026
Primary completion date
31 Dec 2026
Lead sponsor
Bangladesh Medical University
Diseases
Depression
NCT number
NCT07579078

What you commit to

  • Study type: Interventional
  • Planned participants: 34
  • From 25 Apr 2026 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known hypersensitivity to vitamin D
  • Presence of any other serious psychiatric or systemic illness

Other

  • Active smokers
  • Pregnant women
  • Lactating women
  • Women taking hormonal contraceptives.
  • Individuals already taking vitamin D supplements
  • Patients with hypercalcemia

Who the study is looking for

  • • Diagnosed case of MDD by a psychiatrist form the Department of Psychiatry OPD, based on the Diagnostic and Statistical Manual of Mental Disorder, 5th edition (DSM-V) criteria set by the American Psychiatric Association.
    • Hypovitaminosis D ( serum 25 ( OH )D \<30 ng/ml )
    • Age range : 20-40 years
    • Sex: female
    • Patients must be on a stable dose regimen, without any changes in drug type or dosage, for at least 6 months prior to enrollment , to minimize confounding effects on EEG outcomes.
    • Not receiving any medication that affect central nervous system other than anti-depressant drugs

Age in the registry: 20 years to 40 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bangladesh Medical University
Coordinator of this site? Confirm its status
DhakaBangladeshUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.