1/2-Optimizing PTSD Treatments
1/2-优化 PTSD 治疗
基本信息
- 批准号:8402639
- 负责人:
- 金额:$ 52.58万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2004
- 资助国家:美国
- 起止时间:2004-01-01 至 2015-01-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAftercareBiologicalCaringChronicClientCombined Modality TherapyComplexDiagnosisDiagnosticEffectivenessExposure toFemaleGeneticHydrocortisoneIndividualInstitute of Medicine (U.S.)InterventionKnowledgeLong-Term EffectsMajor Depressive DisorderMeasuresMedicineModalityOutcomeParticipantPatient CarePatient PreferencesPatientsPharmacological TreatmentPharmacotherapyPost-Traumatic Stress DisordersProcessPsychopathologyPsychotherapyRandomizedRecruitment ActivityRelative (related person)ReportingResearchRoleSamplingSertralineSocial supportStrategic PlanningSurvivorsSymptomsTherapeuticTraumaTreatment EffectivenessZoloftactive methodbiopsychosocialcost effectivenessfollow-upfunctional disabilitymalepreferencepsychologicpsychosocialrandomized trialresponse markertreatment adherencetreatment effecttreatment response
项目摘要
DESCRIPTION (provided by applicant): Although it is well established that both pharmacological and psychological therapies are relatively effective in treating chronic posttraumatic stress disorder (PTSD), the recent Institute of Medicine (IOM, 2007) report highlights vast gaps in our current knowledge noting a lack of knowledge regarding factors influencing treatment acceptance and completion, the combined effectiveness of these pharmacological and psychological treatment, and their efficacy in common subpopulations (e.g., those with diagnostic co-occurrence). To address these gaps, we propose the first large-scale trial to directly focus on individualizing PTSD care across several key parameters: choice of treatment, the effects of combined psychotherapy and pharmacological PTSD treatment, and the presence of co-occurring major depression. Building on our previous psychotherapy and pharmacotherapy trial on PTSD treatment, we will conduct a doubly randomized preference trial in which female and male trauma survivors with chronic PTSD will be randomly assigned to either choice or no choice treatment conditions. In the choice condition, patients will choose between prolonged exposure (PE) and prolonged exposure plus sertraline (PE + SER). In the no choice condition, patients will be randomly assigned to either prolonged exposure alone (PE) or prolonged exposure plus sertraline (PE + SER). In addition, we will specifically recruit and examine patients with co-occurring major depressive disorder (MDD). Outcome, as measured by both psychopathology and broader functioning measures, will be assessed at post-treatment and through 24-month follow-up. We will also examine biopsychosocial markers of response, psychotherapy change processes, and cost-effectiveness of these treatments. The Specific Aims are: 1) To compare the short-term and long-term effectiveness of PE to that of PE + SER; 2) To systematically compare patients who have chosen their treatment to those who have not in terms of treatment adherence, treatment completion, and effectiveness; and 3) To compare individuals with PTSD alone to those with PTSD and co-occurring major depression. In line with the NIMH's strategic plan, this application focuses on more personalized medicine, focusing on patients' choices and better understanding individual trajectories of outcome.
描述(由申请人提供):尽管已经有充分的确定,药理学和心理疗法在治疗慢性创伤后应激障碍(PTSD)方面均相对有效,但最近的医学研究所(IOM,2007年)报告说,在我们当前的知识中,在我们当前缺乏有关治疗治疗的知识方面的知识的差距很大,这些知识缺乏这些因素,这些因素的综合治疗方法和概念性的效率,以及在这些知识方面的依据,并具有成就,并具有促进性的效率,并具有促进性,并具有成就的效率,并具有成就的影响,并具有促进性的效率,并具有促进性的效率,并具有促进性的效率,并具有促进性的良性,并具有促进性的效率,并具有促进性的效率,并具有良好的知识。 (例如,具有诊断性共发生的人)。为了解决这些差距,我们提出了第一个大规模试验,以直接关注几个关键参数的PTSD护理:治疗的选择,联合心理治疗和药理学PTSD治疗的效果以及共同发生的重大抑郁症的存在。在我们先前的心理治疗和PTSD治疗中的药物治疗试验的基础上,我们将进行一项双随机偏好试验,其中患有慢性PTSD的男性和男性创伤幸存者将被随机分配给选择或没有选择治疗条件。在选择条件下,患者将在长时间暴露(PE)和长时间暴露以及舍曲林(PE + SER)之间进行选择。在别无选择的条件下,患者将被随机分配到长时间暴露(PE)或长时间暴露加上舍曲林(PE + SER)。此外,我们将专门招募并检查患有重大抑郁症(MDD)的患者。通过心理病理学和更广泛的功能措施来衡量的结果将在治疗后和24个月的随访中进行评估。我们还将检查这些治疗方法的反应,心理治疗变化过程以及成本效益的生物心理社会标志。具体目的是:1)将PE与PE + Ser的短期和长期有效性进行比较; 2)系统地将选择治疗的患者与没有治疗依从性,治疗完成和有效性的患者进行比较; 3)仅将PTSD的个体与PTSD和同时发生的重度抑郁症进行比较。根据NIMH的战略计划,该应用集中在更个性化的医学上,重点是患者的选择,并更好地了解各个结果的轨迹。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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{{ truncateString('NORAH C FEENY', 18)}}的其他基金
Treatment of Stress-Related Psychopathology: Targeting Maladaptive and Adaptive Event Processing
压力相关精神病理学的治疗:针对适应不良和适应性事件处理
- 批准号:
10495422 - 财政年份:2020
- 资助金额:
$ 52.58万 - 项目类别:
Treatment of Stress-Related Psychopathology: Targeting Maladaptive and Adaptive Event Processing
压力相关精神病理学的治疗:针对适应不良和适应性事件处理
- 批准号:
10188644 - 财政年份:2020
- 资助金额:
$ 52.58万 - 项目类别:
TREATMENT FOR PTSD: PROLONGED EXPOSURE THERAPY VS ZOLOFT
创伤后应激障碍 (PTSD) 的治疗:长期暴露疗法 VS 佐洛复
- 批准号:
7378056 - 财政年份:2006
- 资助金额:
$ 52.58万 - 项目类别:
TREATMENT FOR PTSD: PROLONGED EXPOSURE THERAPY VS ZOLOFT
创伤后应激障碍 (PTSD) 的治疗:长期暴露疗法 VS 佐洛复
- 批准号:
7202788 - 财政年份:2005
- 资助金额:
$ 52.58万 - 项目类别:
TREATMENT FOR ADOLESCENTS WITH DEPRESSION STUDY (TADS)
青少年抑郁症治疗研究 (TADS)
- 批准号:
7202759 - 财政年份:2005
- 资助金额:
$ 52.58万 - 项目类别:
Effectiveness of PTSD Treatment: PE vs Zoloft
PTSD 治疗的有效性:PE 与左洛复
- 批准号:
6727917 - 财政年份:2004
- 资助金额:
$ 52.58万 - 项目类别:
Effectiveness of PTSD Treatment: PE vs Zoloft
PTSD 治疗的有效性:PE 与左洛复
- 批准号:
7007661 - 财政年份:2004
- 资助金额:
$ 52.58万 - 项目类别:
Effectiveness of PTSD Treatment: PE vs Zoloft
PTSD 治疗的有效性:PE 与左洛复
- 批准号:
6840418 - 财政年份:2004
- 资助金额:
$ 52.58万 - 项目类别:
Prolonged exposure therapy or Zoloft for posttraumatic stress disorder in women
长期暴露疗法或左洛复治疗女性创伤后应激障碍
- 批准号:
6974978 - 财政年份:2004
- 资助金额:
$ 52.58万 - 项目类别:
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