Bright Light Treatment of Combat-related PTSD: A Randomized Controlled Trial

被引:16
|
作者
Youngstedt, Shawn D. [1 ,2 ]
Kline, Christopher E. [3 ]
Reynolds, Alexandria M. [4 ]
Crowley, Shannon K. [5 ]
Burch, James B. [6 ]
Khan, Nidha [7 ]
Han, SeungYong [1 ]
机构
[1] Arizona State Univ, Edson Coll Nursing & Hlth Innovat, Phoenix, AZ 85004 USA
[2] Phoenix VA Hlth Care Syst, Phoenix, AZ 85012 USA
[3] Univ Pittsburgh, Dept Hlth & Human Dev, Res Serv, Pittsburgh, PA 15261 USA
[4] Univ Virginia, Dept Psychol, Coll Wise, Wise, VA 24293 USA
[5] North Carolina Wesleyan Coll, Dept Exercise Sci, Dept Hlth Promot, Rocky Mount, NC 27804 USA
[6] Univ South Carolina, Dept Epidemiol & Biostat, Columbia, SC 29208 USA
[7] Univ South Carolina, Dept Environm Hlth Sci, Columbia, SC 29208 USA
关键词
POSTTRAUMATIC-STRESS-DISORDER; SEASONAL AFFECTIVE-DISORDER; SLEEP QUALITY INDEX; NONSEASONAL DEPRESSION; VETERANS; EFFICACY; PLACEBO; DEPLOYMENT; SERTRALINE; INTERVIEW;
D O I
10.1093/milmed/usab014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Post-traumatic stress disorder (PTSD) is a prevalent consequence of combat with significant associated morbidity. Available treatments for PTSD have had limitations, suggesting a need to explore alternative or adjuvant treatments. Numerous rationales for bright light treatment of PTSD include its benefits for common PTSD comorbidities of depression, anxiety, and circadian misalignment and its relative ease of use with few side effects. The primary aims of this research were to examine the effects of bright light treatment for combat-related PTSD and associated morbidity. Materials and Methods A randomized controlled trial was performed in N = 69 veterans with PTSD attributable to combat in Afghanistan and/or Iraq. Following a 1-week baseline, participants were randomized to 4 weeks of daily morning bright light treatment (10,000 lux for 30 min/day) or a control treatment (inactivated negative ion generator). At baseline and at the end of treatment, participants were rated blindly on the Clinician Assessed PTSD Scale (CAPS), the Clinical Global Impressions Scale (CGI), and the Hamilton Depression Scale and rated themselves on the PTSD Checklist-Military (PCL-M). Following baseline and each treatment week, participants completed self-reported scales of state anxiety, depression, and sleep, and sleep and the circadian rhythm of wrist activity were also assessed with wrist actigraphy. Results Compared with the control treatment, bright light elicited significantly greater improvements in the CAPS and CGI-Improvement. The bright light also elicited a significantly greater rate of treatment response (reduction >= 33%) for the CAPS (44.1% vs. 8.6%) and PCL-M (33% vs. 6%), but no participant had remission from PTSD. Changes in depression, anxiety, and sleep did not differ between treatments. Improvement in CAPS was significantly correlated with a phase advance of the circadian rhythm of wrist activity. Conclusions The most comprehensive study on the topic to date indicated significant short-term efficacy of bright light treatment on the primary variables (CAPS and CGI) with clinical relevance (i.e., treatment response) in veterans with chronic PTSD who did not report extremely high habitual light exposure. No significant effects were found for anxiety, depression, or sleep disturbance. Further research is warranted, particularly exploration of circadian phase-shifting mechanisms of bright light for PTSD.
引用
收藏
页码:E435 / E444
页数:10
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