At present, the treatment of Bipolar I disorder (BD-I), especially its depressive episode (bipolar depression), is still limited, because there is no effective treatment for the associated cognitive impairment and perceived stress. NMDA receptor (NMDAR) dysfunction is associated with BD-I, particularly its cognitive impairment and perceived stress. This study aims to examine the efficacy and safety of an NMDA enhancer (NMDAE) in the treatment of cognitive impairment and perceived stress in the patients with bipolar depression.
Bipolar I disorder (BD-I) is a severe brain disorder. At present, the treatment of BD-I, especially its depressive episode (bipolar depression), is still limited, because there is no effective treatment for the associated cognitive impairment and perceived stress. This study aims to examine the efficacy and safety of an NMDA enhancer (NMDAE) in the treatment of cognitive impairment and perceived stress in the patients with bipolar depression. The subjects are bipolar depression patients. They have been treated for bipolar depression for at least four weeks but remain depressive. Participating in this study, they will continue the original treatment, and will be randomized, double-blindly to receive the NMDAE or placebo for 8 weeks. We will measure 6 cognitive domains (including 9 cognitive tests) and quality of life at weeks 0 and 8; and assess the Perceived Stress Scale, Global Assessment of Function (GAF), various scales for clinical symptoms, and side effects at weeks 0, 2, 4, 6, and 8. The efficacies of NMDAE and placebo will be compared. Chi-square (or Fisher's exact test) will be used to compare differences of categorical variables and t-test (or Mann-Whitney test if the distribution is not normal) for continuous variables between treatment groups. Mean changes from baseline in repeated-measure assessments will be assessed using the generalized estimating equation (GEE). All p values for clinical measures will be based on two-tailed tests with a significance level of 0.05.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
90
Use of an NMDA enhancer for the treatment of bipolar depression
Use of placebo as a comparator.
Department of Psychiatry, China Medical University Hospital
Taichung, Taiwan
RECRUITINGChange in Visual Continuous Performance Test
Assessment of sustained attention
Time frame: week 0, 8
Change in Wisconsin Card Sorting Test
Assessment of abstract and shift set
Time frame: week 0, 8
Change in Logical Memory Test of the Wechsler Memory Scale
Assessment of episodic memory
Time frame: week 0, 8
Digit Span
Assessment of verbal working memory
Time frame: week 0, 8
Spatial Span
Assessment of nonverbal working memory
Time frame: week 0, 8
Category Fluency
Assessment of speed of processing
Time frame: week 0, 8
Trail Marking A
Assessment of speed of processing
Time frame: week 0, 8
WAIS-III Digit Symbol-Coding
Assessment of speed of processing
Time frame: week 0, 8
Mayer-Salovey-Caruso Emotional Intelligence Test (MSCEIT) V2.0
Assessment of social cognition
Time frame: week 0, 8
Change in Perceived Stress Scale in Perceived Stress Scale
Assessment of stress and anxiety symptoms Minimum value: 0, maximum value:56, the higher scores mean a worse outcome.
Time frame: week 0, 2, 4, 6, 8
Change in Quality of life (SF-36)
Time frame: week 0, 8
Change in Global Assessmeint of Functioning
Assessment of global improvement. Minimum value: 1, maximum value:100, the higher scores mean a better outcome.
Time frame: Week 0, 2, 4, 6, 8
Change in Hamilton Rating Scale for Depression
Assessment of depressive symptoms. Minimum value: 0, maximum value:52, the higher scores mean a worse outcome.
Time frame: Week 0, 2, 4, 6, 8
Change in Montgomery-Åsberg Depression Rating Scale
Assessment of depressive symptoms. Minimum value: 0, maximum value:60, the higher scores mean a worse outcome.
Time frame: Week 0, 2, 4, 6, 8
Change in Young Mania Rating Scale
Assessment of manic symptoms. Minimum value: 0, maximum value:60, the higher scores mean a worse outcome.
Time frame: Week 0, 2, 4, 6, 8
Change in Beck Scale for Suicide Ideation
Assessment of Suicide Ideation. Minimum value: 0, maximum value:38, the higher scores mean a greater risk of suicide.
Time frame: Week 0, 2, 4, 6, 8
Change in Clinical Global Impression Scale
Time frame: Week 0, 2, 4, 6, 8
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