Sleep Disturbances and Their Association With Serum Magnesium Level in Patients With Major Depressive Disorder

Assiut University

Status: Begins enrollment in 6 months

Conditions: Sleep Disturbances; Depressive Disorder

Study type: Observational

Funder types: Other

Identifiers

NCT07198477

Mg levels in major depression

Details and patient eligibility

About

This cross-sectional study investigates the relationship between serum magnesium levels and the presence of sleep disturbances among patients with major depressive disorder (MDD).

Full description

Major depressive disorder is a highly prevalent psychiatric condition often accompanied by disabling sleep disturbances, including insomnia and hypersomnia. Evidence suggests that magnesium, a vital trace element involved in neurotransmission, stress response, and circadian regulation, may play a crucial role in both mood and sleep. Low serum magnesium levels have been linked to increased depressive symptom severity and disturbed sleep quality. This study seeks to explore whether hypomagnesemia can serve as a biological contributor to sleep dysfunction in MDD. By employing the Beck Depression Inventory-II (BDI-II) and the Pittsburgh Sleep Quality Index (PSQI), as well as laboratory measurement of serum magnesium levels, the study aims to determine whether lower magnesium is significantly associated with greater depressive burden and poor sleep outcomes. The findings may help validate magnesium as a biomarker for early screening and risk stratification in psychiatric care.

Enrollment: 90 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Confirmed diagnosis of major depressive disorder

age 18 years and older

Ability to complete questionnaires (BDI-II and PSQI; validated Arabic versions)

Willing to participate and provide informed consent

Exclusion criteria

• hronic renal failure or metabolic disorders affecting magnesium balance

Current use of medications known to significantly interfere with serum magnesium (e.g., long-term diuretics, proton pump inhibitors) unless stable and documented

Presence of other comorbid psychiatric disorders

Cognitive impairment or language difficulties preventing questionnaire completion

Trial design

90 participants in 1 patient group

Adult patients with major depressive disorder

Description:

The study sample will include 90 psychiatric patients recruited from the outpatient and inpatient clinics of Assiut University Hospital, representing males and females aged 18-60 years. All participants will have a confirmed diagnosis of major depressive disorder based on clinical criteria and will be evaluated using standardized psychiatric assessment tools.