Neural and Visual Responses to Light in Bipolar Disorder: A Novel Putative Biomarker
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 91
- 试验地点
- 1
- 主要终点
- visual evoked potentials (VEP) waveforms (mean amplitudes or latencies)
研究概览
简要总结
Objective. Bipolar Disorders (BD) are a major public health problem. The investigators still lack knowledge of the mechanisms which contribute to BD. Hence treatments are few and limited, and clinical decision making is less refined. Currently, the investigators are investigating the effects of midday bright light therapy for the treatment of bipolar depression (University of Pittsburgh IRB approved protocol titled Light Therapy for Bipolar Disorder, IRB#: PRO09020546). In this study, the investigators propose to investigate a possible biological mechanism which might explain response to light treatment in depressed bipolar patients.
详细描述
The study goal is to understand how the response to light therapy relates to changes in vision, brain function and improvement in bipolar symptoms. The aims are to investigate mood levels plus the eye and brain responses to visual contrast stimuli in healthy comparators (HC) and bipolar depressed patients.
Study Design and Methods. Overview. The investigators plan to enroll 18-50 year old adults with BD Type I or II and a current episode of major depression on stable-dosed antimanic drugs, and age and sex-matched HC - without mental disorders. Depressed patients with BD will be assigned randomly to receive active light therapy vs inactive comparator for 6 weeks. The investigators will examine responses to contrast stimuli from measures of visual evoked potentials and electro-retinography in HC and depressed bipolar patients before and after 6-weeks of daily midday light therapy. The investigators will assess repeated measures of mood symptom levels, attention and circadian rhythms.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Ages 18-50 years.
- •DSM-IV BD Type I or II, current major depressive episode
- •Stable-dosed antidepressant drug for 4 weeks or more only with concurrent antimanic drug.
- •Controlled thyroid disease.
- •Subjects with preexisting eye diseases will be included specific exceptions are described in the Exclusion Criteria.
- •Able to provide informed consent.
- •Stable minimum dose of antimanic drug for 4weeks or more.
- •Stable unchanged psychotherapy for 16 weeks or more.
- •Permitted drugs for sleep at low doses.
排除标准
- •Certain specific eye diseases (retinal disease, untreated cataracts or macular degeneration)
- •Photosensitizing drugs such as phenothiazines (chlorpromazine), antimalarial drugs, melatonin and hypericum.
- •Acute psychosis (DSM-IV Criteria)
- •Rapid cycling in the past 1 year
- •Alcohol or substance abuse or dependence in the past 6 months.
- •Current symptoms of hypomania or mania i.e. ManiaRatingScale=5
- •Recent history of a suicide attempt (3 months) or active suicidal ideation (SIGH-ADS item H11=2 or more)
- •Treatment with propranolol (Inderal), exogenous melatonin, chronic NSAIDS.
结局指标
主要结局
visual evoked potentials (VEP) waveforms (mean amplitudes or latencies)
时间窗: Week 0 and Week 6
Visual Evoked Potential (VEP). This is a test which is used to assess visual cortical responses. The VEP recordings will be assessed at different contrast levels (80%, 16% and 7%) for the patient groups (BD vs HC). To assess the change in visual cortical responses, we will compare differences in the VEP responses between Weeks 0 and 6 between the groups.
Electroretinography (ERG) waveforms (mean amplitudes or latencies)
时间窗: Week 0 and Week 6
Electroretinogram (ERG). This is a test which is used to assess electrical responses of the retina. The ERG recordings will be assessed at different contrast levels (80%, 16% and 7%) for the patient groups (BD vs HC). To assess the change in retinal responses, we will compare differences in ERG responses between Weeks 0 and 6 between the groups.
次要结局
未报告次要终点
研究者
Dorothy Sit
Associate Professor of Psychiatry and Behavioral Sciences
Northwestern University