An Open Label Study of the Genecept™ Assay to Evaluate Efficacy of Using Assay Guided Treatment in Outpatient Adults With Treatment Resistant Depression
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 2
- 主要终点
- Efficacy
研究概览
简要总结
The purpose of this study is to examine the potential impact of the assay in terms of depression severity as measured by change in Clinical Global Impressions (CGI) scale at 3 months.
详细描述
Genomind is sponsoring an open label study of Assay Guided Treatment (AGT) using the Genecept Assay in adult outpatients with Treatment Resistant Major Depressive Disorder. The Genecept Assay is a Clinical Laboratory Improvement Amendments (CLIA) laboratory validated test being researched to determine if having information about genetic variations impacts patient outcomes.
The proposed investigation will examine the potential impact of the Assay in terms of depression severity as measured by change in CGI scale at 3 months. Secondary measures will assess change in Quick Inventory of Depressive Symptoms (QIDS-SR), Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q) and Zung self-rated anxiety scales at 3 months. Additional measures include change in clinician treatment and diagnosis decisions and impact on mediation side effects using the Udvalg for Kliniske Undersøgelser Side Effect Rating Scale (UKU). Participant data will be compared to a matched control cohort to assess the impact of the use of the Genecept Assay on medication adherence and total claims.
Patients with a diagnosis of non-psychotic Major Depressive Disorder will be identified. These patients and their treating clinicians will be recruited. The present study proposes to enroll 1. Subjects (patients who are identified as eligible) and 2. Clinician study participants (clinicians who are identified as responsible for the care of eligible patients). This study will involve the collection of responses from both Subjects and clinician study participants with the intention of correlating this information to Subject genetic data.
Potential subjects and study participants will consent electronically on a secure study portal. Patients and Clinicians must both consent to participate in order to proceed in the study. After both subjects and clinician study participants have consent to participate, they will each be asked to complete an electronic baseline survey. Once the baseline survey is completed, the clinician will receive the Genecept Assay by mail and will then supervise collection of a saliva DNA sample during a routine office visit.
At baseline, month 1 and month 3, patient Subjects will be prompted to complete surveys which include questions about their psychiatric symptoms, quality of life and medication side effects. The 3 month patient assessment will also include a satisfaction questionnaire.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 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 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 18-65 years
- •Ability to complete electronic informed consent
- •access to appropriate technology (i.e. internet-connected device, internet connection),
- •cognitively competent
- •Eligible participants will have one or more of the following diagnoses for 12 months or longer: 296.2x, 296.3x
- •Must have had self-insured Aetna Behavioral Health, Medical, and Pharmacy benefits for that 12-month period.
- •QIDS-SR score of at least 10 (i.e., moderate depression) at initial visit
- •Must have had an initial prescription plus two refills of two antidepressants from different GPI4 levels.
- •Must have access to the secure web-portal to complete self-assessments
排除标准
- •Clinician selected in conjunction with the patient chooses not to participate
- •Psychotic features in the current episode, based upon clinical assessment
- •Inpatient behavioral health hospitalization within six months prior to the study
- •Four or more failed pharmacologic interventions in the current major depressive episode [response rates for these Subjects is likely to be extremely low and would require a substantially larger-scale study to identify treatment effects]
- •Current substance use disorder assessed as being of a severity that requires inpatient or outpatient detoxification
- •Pregnant women or women of child bearing potential who are not using a medically accepted means of contraception
- •Women who are breastfeeding
- •Serious suicide or homicide risk, as assessed by evaluating clinician
- •Unstable medical illness including cardiovascular, hepatic, renal, respiratory, endocrine, neurological, or hematological disease, based on review of medical history, physical examination, and screening laboratory tests
- •Patients who have taken an investigational psychotropic drug within the last three months
- •Clinician Study Participants:
- •Inclusion Criteria :
- •Treating clinician for potential Patient subjects identified for the study
- •Valid NPI number
- •Signed electronic informed consent
- •Exclusion Criteria:
- •Inability to complete online surveys
- •Patient selected in conjunction with the clinician chooses not to participate
结局指标
主要结局
Efficacy
时间窗: 3 Months
To determine the efficacy of assay-guided treatment (AGT) in terms of illness severity as measured by change from baseline in Clinical Global Impressions (CGI) scale at 3 months.
次要结局
- Medication Adherence(3 months)
- Resource Utilization(3 months)
- Side Effects(3 months)
- Efficacy(3 months)
- Impact of Specific Genetic Variants(3 months)