Dementia Clinical Trial
Official title:
A Randomized Placebo-controlled Trial Evaluating the Effect of Melatonin on Sleep Quality in Patients With Dementia
Introduction: Patients with dementia may suffer from poor sleep quality. Disturbance in the
metabolism melatonin may have a role in the pathogenesis of sleep-wake cycle alterations in
dementia.
Objective: To evaluate the efficacy of low dose exogenous melatonin in improving sleep
quality.
Design: A single-center randomized, double-blinded, placebo-controlled study carried out on
outpatients with dementia and sleep alterations.
Participants: The investigators calculated a 40 individuals aged 65 years or over with a
diagnosis of mild-moderate dementia (Clinical Dementia Rating 1-2).
Intervention: Patients were randomized to receive either 5 mg of melatonin or placebo every
night for 8 weeks.
Measurements: The primary outcome was sleep quality according to the Pittsburgh Sleep
Quality Index (PSQI).
This is a single-center study. The study protocol, informed consents, and amendments were
approved in writing by the appropriate local site Independent Ethics Committee
(IEC)/Institutional Review Boards (IRB) (Ethics Committee of the Universidad Autónoma de
Nuevo León, School of Medicine).
The patients were recruited as outpatients from the Geriatrics Clinic. A total of 67
patients were screened out of which 40 male and female patients diagnosed with mild to
moderate dementia were recruited to the study. Following inclusion, all patients underwent
randomization to treatment with melatonin (5 mg orally) or placebo for 8 weeks. To prevent
bias, matching placebo tablets, which were identical in appearance, taste, and odor, were
used. The treatment was double-blinded, with two parallel treatment groups. Selection for a
treatment group was determined by a computer-generated randomization list, in a 1:1 ratio
using the randomized permuted blocks method.
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