睡眠机制知识库

MELODY 试验:辅助褪黑素、数字化失眠认知行为治疗或安慰剂改善心境障碍青年抑郁症状的 12 周随机对照试验研究方案

MELODY trial: study protocol for a 12-week randomised controlled trial of adjunctive melatonin, digital cognitive behavioural therapy for insomnia or pill placebo to improve depressive symptoms in young adults with mood disorders.

原始研究开放获取
作者
Crouse JJ, Shin M, Hockey SJ, Jeon E, Bradshaw N, Nichles A, Zmicerevska N, Chong MK, You H, Wray NR, Scott J, Grunstein RR, Naismith SL, Merikangas KR, Cain SW, Medland SE, Iorfino F, Uebergang TD, McKenna S, Carpenter JS, Tonini E, Bhattacharya N, Hamilton BA, Wallace LM, Henders AK, Scott EM, Song YJC, Brain and Mind Centre Lived Experience Working Group, Hickie IB 等
期刊
BMJ open
出处
2026; 16(8); e114817
DOI
10.1136/bmjopen-2025-114817
PMID
42637255
被引
1

一句话摘要

MELODY 试验方案:单中心 3 期随机对照试验,660 名 18—30 岁重性抑郁或双相 II 型障碍青年随机接受 12 周辅助褪黑素、数字化失眠认知行为治疗(dCBT-I)或安慰剂,主要终点为第 12 周抑郁症状。

为什么重要

直接检验「睡眠与节律治疗能否抗抑郁」这一未决临床问题,是该领域少见的大样本、设盲、以抑郁为主要终点的设计。(本条为研究方案,尚无结果。)

英文摘要原文

Sleep and circadian rhythm disturbances are proposed to be pathophysiological mechanisms underlying some cases of depressive and bipolar (mood) disorders. An unresolved clinical question is whether sleep and circadian-based therapies are effective antidepressants for young adults (18-30 years) with a mood disorder. MELODY (Melatonin for Depression in Youth) is an investigator-initiated, single-centre, phase 3, randomised controlled trial with two blinded pharmacological arms (melatonin vs placebo) and one open-label digital intervention arm (digital cognitive behavioural therapy for insomnia (dCBT-I)). The trial is testing whether 12 weeks of adjunctive melatonin or dCBT-I are more effective than pill placebo at reducing depressive symptoms in 660 young people aged 18-30 years with a Structured Clinical Interview for (Diagnostic and Statistical Manual of Mental Disorders, fifth edition; SCID-5) diagnosis of Major Depressive Disorder or Bipolar Disorder type II, moderate to severe depressive symptoms and significant sleep or sleep-wake complaints. The week 12 primary outcome is depressive symptoms (Quick Inventory of Depressive Symptomatology, Adolescent version). Secondary outcomes include partial remission of the Major Depressive Episode (SCID-5) and change in other mental health symptoms, sleep, functioning or quality of life. A subset of participants will undergo in-home assessment of sleep physiology (Sleep Profiler) and in-lab assessment of circadian rhythms (dim-light melatonin onset) to examine biological changes. A 6-month follow-up will explore durability of treatment effects. Mediation analyses will test whether sleep or circadian rhythm changes play a causal role in antidepressant effects. MELODY has been reviewed and approved by the Human Research Ethics Committee (HREC) of the Sydney Local Health District (HREC Approval Number: X23-0450, Protocol version: 1.4, 7/7/25). The findings of the MELODY trial will be disseminated into the scientific and clinical communities via refereed publications, talks and other professional and media outlets. The Brain and Mind Centre's Lived Experience Working Group will contribute to dissemination of MELODY's findings via youth-friendly methods (eg, social media videos, explainers). ACTRN12624000017527.

所属章节

昼夜节律与视交叉上核、分子钟 睡眠障碍病理生理

随机对照试验 褪黑素 dCBT-I 心境障碍 研究方案

条目编号 P152 · 元数据经 Crossref / Europe PMC 回查