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临床试验/NCT03363529
NCT03363529
已完成
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ROOM-LIGHT: Dynamic LED-light as Treatment for Depressed Patients in Inpatient Wards: A Feasibility Trial

University Hospital Bispebjerg and Frederiksberg1 个研究点 分布在 1 个国家目标入组 15 人2017年11月16日

概览

阶段
不适用
干预措施
Standard
疾病 / 适应症
Depression
发起方
University Hospital Bispebjerg and Frederiksberg
入组人数
15
试验地点
1
主要终点
Difference in numbers of drop out in the two groups
状态
已完成
最后更新
2个月前

概览

简要总结

Depression is a major health challenge, and despite developments in pharmacotherapy and psychotherapy a substantial part of patients will only recover very slowly and incompletely, and 10-25 % of the patients are resistant to treatment. Therefore, new treatment initiatives are in demand. Chronotherapeutics can regulate diurnal rhythms and sleep, and have shown promising results on antidepressant effects. Among chronotherapeutic treatment modalities, Bright Light Therapy (BLT) has been used in treatment of depression and sleep disorders for several decades with both an antidepressant and a sleep improving effect. BLT has also been shown to augment antidepressant therapy.

Objectives. The objective of this trial is to investigate the feasibility of a combination of LED-light armatures aiming to mimic sunlight, when installed in the patient rooms of a psychiatric inpatient Ward. Investigators has opted for using a randomized design that will subsequently be tested in a larger clinical trial with depression severity as the primary outcome. In this feasibility study investigators will register the stability of the system, the influence of the light on patients regarding tolerability, comfort, depression level, and sleep. Investigators also so want to measure and collect specific light-data on the Non-image-forming light (NIF) by using specially designed light sensors to capture the spectral distribution of the light. Finally investigators will test the electronic case report form (eCRF) that has been designed for the trial.

Design. The design is a randomised controlled feasibility trial with two arms: an active dynamic light trial arm and a standard light trial arm with blinding of depression outcome assessors (Hamilton depression rating scale), data collection, and data analyses. Randomization will be with a rate for active and standard of 2 to 1.

详细描述

Inclusion and exclusion criteria. Inclusion: Major depression disorder, age \> 18 years, informed consent and Danish speaking. Exclusion: Severe suicidality, actual psychotic state, bipolar disorder and if the patient is subject to coercive measures of any kind. Name and description of experimental and control intervention. The experimental intervention is the implementation of a dynamic LED-light system in two patient rooms. The system includes three elements: a window jamb built-in light panel, two ceiling mounted lamps, and a wall mounted lamp. All lamps will have a dynamic, time dependent frequency distribution and intensity of light. The control intervention is constant standard LED-light with two elements: two ceiling mounted lamps and a wall mounted lamp. Primary and secondary outcomes. Primary outcome: 1\. Rate of patients discontinuing the trial due to discomfort from the lighting condition. Secondary outcomes: 1. Mean scores on the visual comfort scale in the intervention period 2. Reduction in HAM-D17 scores from baseline to week 4 Trial size. In total 15 patients. All regulatory approvals has been met from the Danish Data Protection Agency, the regional Ethics Committee Agency, and the Mental Health Services of Copenhagen. Time schedule. The first participant is expected to be enrolled in December 2017. The expected last follow-up of the last participant will be June 2018. Data will be analysed from June 2018 till December 2018. Manuscripts will be prepared from June 2017 and we expect to submit first manuscript January 2019.

注册库
clinicaltrials.gov
开始日期
2017年11月16日
结束日期
2019年3月19日
最后更新
2个月前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
University Hospital Bispebjerg and Frederiksberg
责任方
Principal Investigator
主要研究者

Klaus Martiny

Professor of Clinical Psychiatry

University Hospital Bispebjerg and Frederiksberg

入排标准

入选标准

  • Major depression disorder
  • Age \> 18 years
  • Informed consent and Danish speaking.

排除标准

  • Severe suicidality
  • Actual psychotic state
  • Bipolar disorder
  • Patient is subject to coercive measures of any kind.

研究组 & 干预措施

Standard

This study arm utilizes a standard lighting condition in the patient room

干预措施: Standard

Dynamic

This study arm utilizes a dynamic lighting from special designed lightfixtures in the ceiling and window sill.

干预措施: Dynamic light

结局指标

主要结局

Difference in numbers of drop out in the two groups

时间窗: Week 4

Number of patients in the two groups that drop out due to the standard or experimental lighting condition

次要结局

  • Visual comfort questionaire(Week 4)
  • Change of depression level from baseline to endpoint(Change scores from baseline to week 4)

研究点 (1)

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