BUMC--JETTE
BUMC--杰特
基本信息
- 批准号:8378989
- 负责人:
- 金额:$ 5.18万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至 2016-05-31
- 项目状态:已结题
- 来源:
- 关键词:Activities of Daily LivingAffectAgingAnimal ModelAnimalsBostonCalibrationCertificationChronicClinical ResearchClinical TrialsDevelopmentDistalElderlyEquilibriumEquipmentEvaluationFatigueFosteringGaitHumanHuman ResourcesImpairmentIndividualInstitutionalizationIntervention StudiesLaboratoriesLeadershipLifeMaizeMeasurementMeasuresMusMuscleNursing HomesObservational StudyOutcomePerformancePhenotypePhysical FunctionPhysical assessmentPrevalenceProtocols documentationQualifyingRattusResearch InfrastructureResearch PersonnelResourcesRodentSkeletal MuscleSpeedStructureTechniquesTestingTrainingTreatment EfficacyUnited StatesWalkingdisabilityexperiencefunctional disabilityinstrumentinterdisciplinary collaborationmortalitymuscle strengthnovel therapeutic interventionperformance testspressuresarcopeniatooltranslational approach
项目摘要
Although the prevalence of chronic disability in older individuals remains on the decline in the United States,
the total number of individuals over the age of 65 with chronic disability is increasing (1, 2). Presently,
limitations in mobility affect almost one in four individuals over age 65 and three quarters of those living in
nursing homes (3). In non-disabled older individuals, limitations in mobility in such tasks as climbing stairs,
and walking across a room have been defined as "mobility disability" (4). To capture and assess mobility
limitations in the elderly, performance tests of functional capacity have been developed and have been shown
to be predictive of incident disability, institutionalization, and mortality (4, 5). In particular, walking ability alone,
as measured by gait speed during a 4 M walk test, has been shown to be a strong predictor of subsequent
ADL disability and mobility disability (6). In addition, validated highly reliable instruments to assess
components of physical disability have also been developed and implemented in observational studies and
clinical trials. More recently, testing protocols in selected animal models (rats, mice) have been developed to
assess important endpoints related to impairments and functional limitations in these species.
尽管在美国,老年人慢性残疾的患病率仍在下降,
65岁以上慢性残疾人的总人数正在增加(1、2)。目前,
行动不便影响到近四分之一的65岁以上的人,四分之三的65岁以上的人,
养老院(3)。在非残疾老年人中,在爬楼梯等任务中的移动性限制,
和在房间里行走被定义为“行动不便”(4)。捕捉和评估流动性
在老年人的限制,功能能力的性能测试已经开发出来,并已被证明
预测事故残疾,机构化和死亡率(4,5)。尤其是行走能力,
如在4米步行测试期间通过步态速度测量的,已经被证明是随后的
ADL残疾和行动能力残疾(6)。此外,经验证的高度可靠的工具,以评估
还在观察性研究中制定和实施了身体残疾的组成部分,
临床试验最近,在选定的动物模型(大鼠、小鼠)中的测试方案已经被开发,
评估与这些物种的损伤和功能限制相关的重要终点。
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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ALAN Maurice JETTE其他文献
ALAN Maurice JETTE的其他文献
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{{ truncateString('ALAN Maurice JETTE', 18)}}的其他基金
Overcoming Challenges to Conducting Disability-Related Comparative Effectiveness
克服开展与残疾相关的比较有效性的挑战
- 批准号:
8287758 - 财政年份:2012
- 资助金额:
$ 5.18万 - 项目类别:
Improving Outcome Measurement for Medical Rehabilitaiton Clinical Trials
改善医疗康复临床试验的结果测量
- 批准号:
7946547 - 财政年份:2010
- 资助金额:
$ 5.18万 - 项目类别:
Improving Outcome Measurement for Medical Rehabilitaiton Clinical Trials
改善医疗康复临床试验的结果测量
- 批准号:
8470201 - 财政年份:2010
- 资助金额:
$ 5.18万 - 项目类别:
Improving Outcome Measurement for Medical Rehabilitaiton Clinical Trials
改善医疗康复临床试验的结果测量
- 批准号:
8146939 - 财政年份:2010
- 资助金额:
$ 5.18万 - 项目类别:
Improving Outcome Measurement for Medical Rehabilitaiton Clinical Trials
改善医疗康复临床试验的结果测量
- 批准号:
8298075 - 财政年份:2010
- 资助金额:
$ 5.18万 - 项目类别:
Improving Outcome Measurement for Medical Rehabilitaiton Clinical Trials
改善医疗康复临床试验的结果测量
- 批准号:
8688289 - 财政年份:2010
- 资助金额:
$ 5.18万 - 项目类别:
PROS (Patient Reported Outcomes) for Children and Young Adults with Disabilities
针对残疾儿童和青少年的 PROS(患者报告结果)
- 批准号:
8334382 - 财政年份:2009
- 资助金额:
$ 5.18万 - 项目类别:
PROS (Patient Reported Outcomes) for Children and Young Adults with Disabilities
针对残疾儿童和青少年的 PROS(患者报告结果)
- 批准号:
8705684 - 财政年份:2009
- 资助金额:
$ 5.18万 - 项目类别:
Efficacy of a Post-Rehabilitation Exercise Intervention
康复后运动干预的功效
- 批准号:
7848230 - 财政年份:2007
- 资助金额:
$ 5.18万 - 项目类别:
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Hormone therapy, age of menopause, previous parity, and APOE genotype affect cognition in aging humans.
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