Genomics
基因组学
基本信息
- 批准号:7944539
- 负责人:
- 金额:$ 15.73万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-08-19 至 2014-06-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAnxietyAreaArizonaBeck depression inventoryCancer CenterCancer Center Support GrantCaringChildClient satisfactionClinicClinicalCognitiveConfusionDataData AnalysesDevelopmentDiagnosticEventFamilyGenomicsGoalsGoldGrantHealthHealth Care VisitHyperactive behaviorInformation SystemsInterviewLanguageLengthLifeLightMeasurementMeasuresMental HealthMental Health ServicesModelingNational Institute of Mental HealthOutcomePatient Outcomes AssessmentsPatientsPerinatalPhasePhysiciansPostpartum DepressionPostpartum WomenPregnancyPrivate SectorProblem behaviorProcessPsychopathologyPublic SectorRecommendationRecruitment ActivityResearchResearch PersonnelRiskSamplingScotlandScreening procedureServicesSiteSmall Business Innovation Research GrantStructureSurveysSymptomsTechnologyTestingTimeUnited StatesValidationVisitWomanbasedepresseddepressiondepressive symptomsexperiencehigh riskimprovedinattentioninstrumentinterestmaternal depressionmenphrasespregnantprogramspsychologicresponsesatisfactionsoundsuccesstime use
项目摘要
Estimates of antenatal and postpartum depression vary from 7% to upwards of 30%
depending on criteria for depression, the type of assessment used, and the timing of the
assessment. Thus, approximately 320,000 to over 1 million women each year
experience symptoms of perinatal depression. Estimates of antenatal depression are
harder to obtain because of the lack of appropriate diagnostic criteria. Despite this, no
screener currently exists that has been developed and tested with both antenatal and
postpartum women that uses concise, simple language, and a consistent response
option set.
The overall aim of this project is to develop a brief screener to assess depressive
symptoms among antenatal and postpartum women. The proposed screener will be
easier for patients to understand, will take less time, and will be more psychometrically
sound than current screeners.
In Phase I we will develop approximately 30 items that are specific to depression in
antenatal and postpartum women. We will test these items using cognitive interviewing
among a sample of 10 antenatal and 10 postpartum women in addition to 32 general
depression items we have previously developed. Experts will review the results of the
cognitive interviewing to develop the item pool that will be tested in Phase II. The Phase
II item pool will consist of at least 20 general depression items, 10 items specific to
antenatal women, and 10 items specific to postpartum women.
In Phase II, 500 antenatal and 500 postpartum women (70% from private sector sites
and 30% from public sector sites) will complete the EPDS (as a screener into the study),
BDI-II, the PROMIS depression items, our items, and the depression module of the
SCID. IRT analyses will be conducted on these data to develop a 7-9 item screener. We
anticipate that approximately 5-7 of these items will be applicable to both antenatal and
postpartum women and approximately 2-3 of these items will be sample specific. The
developed screener will then be given to 400 women who will take the survey twice,
approximately 4-7 days apart. Conclusions regarding test-retest reliability and patient
satisfaction with taking the screener using different modes of technologies will be made
from this study.
产前和产后抑郁症的估计从7%到30%以上不等
项目成果
期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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George S Watts的其他文献
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