首页> 外文期刊>Contemporary Clinical Trials Communications >Prescribing laughter to ameliorate mental health, sleep, and wellbeing in university students: A protocol for a feasibility study of a randomised controlled trial
【24h】

Prescribing laughter to ameliorate mental health, sleep, and wellbeing in university students: A protocol for a feasibility study of a randomised controlled trial

机译:在大学生中提出精神健康,睡眠和福祉的笑声:一种随机对照试验的可行性研究的协议

获取原文
           

摘要

ObjectivesThis research is the first study to investigate the potential effects of a laughter prescription on both psychological health and objective sleep parameters in university students. The primary objective is to evaluate the feasibility of prescribing laughter to inform a larger randomised controlled trial. Secondary objectives are to assess if a two-week laughter prescription improves subjective and objective sleep outcomes, wellbeing, and/or psychological health outcomes.Trial designTo assess the feasibility of a randomised controlled trial for laughter prescription in relation to sleep, psychological health, and wellbeing. Forty university students will be recruited and randomised to one of two conditions (control/experimental).MethodsWrist actigraphy and sleep diaries will be used to estimate sleep outcomes during a one-week baseline testing phase and across the two-week intervention. The experimental group will be shown how to record a Laughie (a 1-min recording of their joyful laughter on their smartphone) and prescribed to laugh with it three times daily for 14 days (the control group will only track sleep). All participants will complete the WHO (Five) Well-being Index, and Hospital Anxiety and Depression Scale pre- and post-intervention. The CONSORT checklist, and the Feasibility, Reach-out, Acceptability, Maintenance, Efficacy, Implementation, and Tailorabilty (FRAME-IT) framework will guide intervention planning and evaluation. Participant interviews will be analysed using Differential Qualitative Analysis (DQA).ResultsThe feasibility of a two-week laughter prescription in university students and its impact on sleep, wellbeing, and/or psychological health outcomes will be assessed.ConclusionsZayed University Research Ethics Committee approved the study in July 2019. The research will be completed following protocol publication.Trial registrationClinicalTrials.gov. ID: NCT04171245. Date of registration: 18 October 2019.
机译:Objectivesthis研究是研究笑声处方对大学生心理健康和客观睡眠参数的潜在影响的研究。主要目标是评估规定笑声的可行性,以通知更大的随机对照试验。次要目标是评估为期两周的笑声处方,提高主观和客观睡眠结果,福祉和/或心理健康结果.TRIAL设计,评估随机对照试验对睡眠,心理健康和心理健康方面的笑声处方的可行性福利。将招募和随机招募四十人学生(控制/实验)。在一周的基线测试阶段和整个两周的干预期间,方法将用于估算睡眠成果。实验组将显示如何记录一个笑(在他们的智能手机上一钟的快乐笑声),并规定每天三次嘲笑14天(对照组只会追踪睡眠)。所有参与者将完成世卫组织(五)福祉指数,以及医院焦虑和抑郁症预测,后期和后期。联盟清单以及可行性,伸展,可接受性,维护,效力,实施和量身框架(框架 - IT)框架将指导干预计划和评估。将使用差分定性分析(DQA)分析参与者访谈。将评估大学生两周笑声处方的可行性及其对睡眠,福祉和/或心理健康成果的影响.Conclusionszay大学研究道德委员会批准2019年7月的研究。该研究将完成以下协议公开.TRIAL CONDIONCLINICALTIALS.GOV。 ID:NCT04171245。日期(注册):2019年10月18日。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号