Effect of Bright Light Therapy on Depression Symptoms in Adult Inpatients With Cystic Fibrosis (CF) and Chronic Obstructive Pulmonary Disease (COPD)
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- 入组人数
- 4
- 试验地点
- 4
- 主要终点
- Change in Pre- and Post-intervention Beck's Depression Inventory II Scores (BDI-II)
研究概览
简要总结
This is a project that will determine whether the use of daily bright light therapy has an effect on depressive symptoms experienced by adult inpatients with CF and COPD. The purpose of this project is to apply a daily 30-minute BLT intervention to hospitalized adult CF and COPD patients in order to decrease symptoms of depression as measured by depression inventory scoring.
详细描述
This project will occur on a 29-bed pulmonary step-down unit at a 1,600-bed academic medical center. This unit commonly treats patients with CF, COPD, and other pulmonary complications. The unit's patient care staff will be educated on the bright light lamps in order to prevent interruptions and to encourage compliance.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosed with cystic fibrosis or chronic obstructive pulmonary disease (COPD)
- •Adult age 18 or older
- •Admitted to the pulmonary step-down and transplant unit
- •Score greater than zero on pre-intervention Beck's Depression Inventory-II (BDI-II)
排除标准
- •Pre-existing ophthalmological conditions or photosensitivity
- •Migraines
- •Receiving high dose steroids for transplant rejection (due to mood altering qualities),
- •Antibiotics that increase light sensitivity
- •Diagnosed with bipolar disorder (light therapy may trigger mania)
- •Admissions anticipated to span less than 48 hours
- •Children are being excluded due to the fact that only adult CF and COPD subjects are admitted to University of Pittsburgh Medical Center (UPMC) Presbyterian hospital
结局指标
主要结局
Change in Pre- and Post-intervention Beck's Depression Inventory II Scores (BDI-II)
时间窗: First at time of admission, second at end of 7 day goal or upon discharge.
Change between pre-intervention and post-intervention self-reported answer totals to the 21 scored items on BDI-II (minimum score obtainable=0 (absent symptoms); maximum score obtainable=63 (most severe symptoms).
次要结局
- Number of Days Until Completion of Daily Bright Light Therapy (BLT)(Daily for duration of intervention period (goal/maximum of 7 days).)
研究者
Erica Osborn
Principal Investigator
University of Pittsburgh