Rolling Julie, Reynaud Eve, Mengin Amaury C, Zanfonato Thomas, Bourgin Patrice, Schroder Carmen M
Department of Child and Adolescent Psychiatry, Strasbourg University Hospitals, Strasbourg, France.
Regional Center for Psychotrauma Great East, Strasbourg University Hospital, Strasbourg, France.
Eur J Psychotraumatol. 2025 Dec;16(1):2474375. doi: 10.1080/20008066.2025.2474375. Epub 2025 Apr 17.
: Sleep disorders in the insomnia spectrum, as well as nightmares, are among the most sensitive and persistent symptoms in children with post-traumatic stress disorder (PTSD). There is currently no reference treatment or specific pharmacological treatment recommendation on the management of sleep disturbances in children and adolescents suffering from PTSD, despite the fact that they have a significant effect on daytime functioning and overall mental health of children as well as on family's health and quality of life. In this respect, paediatric prolonged-release melatonin (PedPRM) has shown significant beneficial effects on insomnia disorders in children with autism spectrum disorders and positive effects on anxiety and depressive symptomatology. Our study will be the first randomized controlled trial to examine the efficacy of PedPRM melatonin on sleep disorders in children and adolescents with PTSD, as well as on PTSD symptoms, associated daytime functioning and overall mental health in these children and their caregivers.: The MelatoSOM-Kids-PTSD study (French national hospital-based clinical research programme) will be a multi-centre prospective double-blind placebo-controlled parallel group clinical trial investigating the efficacy of paediatric prolonged-release melatonin to alleviate sleep disturbances in children and adolescents with PTSD (120 participants recruited over a 24-month period). The experimental group will be treated with active prolonged-release melatonin over 13 weeks (PedPRM). The control group will receive a placebo. The primary endpoint will be the difference in sleep diary derived total sleep time after 13 weeks of treatment in the PedPRM group versus placebo group. Secondary endpoints will be the differences in objective sleep quality parameters and daytime functioning before and after treatment, in children with PTSD and their caregivers.: This paper describes the MelatoSOM-Kids-PTSD protocol, which will evaluate the effectiveness of melatonin, a treatment that has already demonstrated an excellent benefit-risk ratio in the paediatric population over 4 years.
失眠谱系中的睡眠障碍以及噩梦,是创伤后应激障碍(PTSD)儿童中最敏感且持续存在的症状之一。尽管睡眠障碍对儿童的日间功能、整体心理健康以及家庭健康和生活质量有重大影响,但目前对于患有PTSD的儿童和青少年的睡眠障碍管理,尚无参考治疗方法或具体的药物治疗建议。在这方面,儿科缓释褪黑素(PedPRM)已显示出对自闭症谱系障碍儿童的失眠症有显著益处,对焦虑和抑郁症状也有积极作用。我们的研究将是第一项随机对照试验,旨在研究PedPRM褪黑素对患有PTSD的儿童和青少年的睡眠障碍、PTSD症状、相关的日间功能以及这些儿童及其照顾者的整体心理健康的疗效。
MelatoSOM-Kids-PTSD研究(法国国家医院临床研究项目)将是一项多中心前瞻性双盲安慰剂对照平行组临床试验,研究儿科缓释褪黑素缓解患有PTSD的儿童和青少年睡眠障碍的疗效(在24个月内招募120名参与者)。实验组将接受为期13周的活性缓释褪黑素(PedPRM)治疗。对照组将接受安慰剂。主要终点将是PedPRM组与安慰剂组在治疗13周后睡眠日记得出的总睡眠时间差异。次要终点将是患有PTSD的儿童及其照顾者在治疗前后客观睡眠质量参数和日间功能的差异。
本文描述了MelatoSOM-Kids-PTSD方案,该方案将评估褪黑素的有效性,褪黑素在4岁以上儿科人群中已显示出极佳的效益风险比。