Incline Training to Personalize Motor Control Interventions after Stroke
Incline Training to Personalize Motor Control Interventions after Stroke
批准号:
10011586
负责人:
Mark G. Bowden
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-07-01 至 2022-06-30
关键词:
AffectAgeBiomechanicsClinicalControl GroupsDataExhibitsFlexorFutureGoalsHip region structureImpairmentIndividualInterventionJointsKineticsKneeLengthMovementOutcomeOutcome MeasureParesisParticipantPatternPhysical therapyPopulation HeterogeneityPredictive FactorProductionPublishingRandomizedRandomized Controlled TrialsRehabilitation therapyResearchStrokeTechniquesTestingTherapeuticTherapeutic InterventionTrainingTranslatingTranslationsVeteransWalkingbasechronic strokeclinical decision-makingclinical effectdisabilityeffective interventionexperiencefollow-upfunctional outcomesimprovedimproved functioningimproved mobilityindividualized medicineinnovationkinematicsleg paresismotor controlpersonalized interventionpersonalized strategiespost strokepredicting responsepredictive modelingrehabilitation strategyresponsestroke rehabilitationstroke survivortheoriestreadmilltreatment effecttreatment strategywalking programwalking rehabilitationwalking speed
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The long term goal of this research is to advance personalization of walking rehabilitation for individuals post-
stroke by developing therapeutic strategies targeting an individual’s specific motor control deficit. Stroke is an
incredibly heterogeneous population, and while various therapeutic approaches have produced large effects in
some individuals, group effects are often minimized by those who fail to respond to the intervention, leading to
a paucity of efficacious randomized controlled trials. In addition, evidence supporting mechanisms by which
walking is improved is limited, and we currently lack models predicting which individuals are likely to respond to
an intervention and the mechanisms by which they improve. An urgent need exists to maximize treatment effect
by targeting specific motor control impairments and improve predictive capability by developing theory-based
clinical decision-making frameworks to translate interventions tailored to specific deficits for walking rehabilitation
after stroke. Our overall goal for this project is to test a motor control deficit-based treatment approach that we
developed, in order to provide information necessary for future translation of personalized interventions. We
previously published the existence of distinct post-stroke motor control deficits based on the percentage of
overall propulsive forces generated by the paretic leg termed paretic propulsion (Pp), a widely accepted
biomechanical outcome measure that we developed. 1) Low Pp is associated with large and early paretic flexor
EMG activity, lengthened paretic step length, and decreased paretic hip extension; and 2) High Pp pattern is
characterized by decreased knee flexion during paretic swing, shortened paretic step length, and prolonged
paretic hip extension. Our pilot data reveal that individuals with these walking patterns are most effectively
rehabilitated by unique treatment strategies: 1) Low Pp by walking on an inclined treadmill requiring increased
force production; and 2) High Pp by walking on a declined treadmill, promoting effective stance to swing
transitions through normalization of joint kinetics and kinematics. The hypothesized ideal training strategy
(INCLINE for low Pp and DECLINE for high Pp) is the personalized strategy and will be compared to non-
personalized strategies (DECLINE for low Pp and INCLINE for high Pp). Both personalized strategies will be
compared to a CONTROL group training on a flat treadmill at equivalent amounts of walking activity. Pilot training
data demonstrate that personalized strategies demonstrate a larger effect on self-selected walking speed
(SSWS) and symmetry of Pp. Thus, the purposes of this proposal are to compare clinical and biomechanical
outcomes from personalized strategies to both non-personalized strategies and control interventions and to
identify the variables that predict meaningful changes in SSWS. To accomplish these purposes, we will equally
randomize 60 individuals (30 with high Pp and 30 with low Pp) between the ages of 25 and 75 with chronic stroke
to one of three interventions (INCLINE, DECLINE, or CONTROL). Training will occur 3x/week for 4 weeks and
will be evaluated pre- and post-training and at a one-month follow-up. Aims will evaluate the improvement in
functional and biomechanical outcomes in both the INCLINE and DECLINE groups compared to a CONROL
group. A third aim will determine the factors that contribute to response to INCLINE and DECLINE training
defined as an improvement of 0.16 m/s in SSWS based on responder outcomes in previous locomotor
rehabilitation trials. Selecting the correct intervention for a given motor control deficit, as opposed to applying a
one-size-fits-all strategy, is likely to aid in maximizing clinical effects of locomotor rehabilitation interventions after
stroke. This approach is based on building capacity to improve motor control deficits as opposed to training
specifically to the targeted functional outcome. Determining the efficacy of personalized interventions on clinical
and biomechanical outcomes and determining the factors that predict response has high likelihood of improving
locomotor rehabilitation for Veterans who have experienced a stroke.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Incline Training to Personalize Motor Control Interventions after Stroke
-
批准号:10189735
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2018
-
负责人:Mark G. Bowden
-
依托单位:
Incline Training to Personalize Motor Control Interventions after Stroke
-
批准号:10641654
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2018
-
负责人:Mark G. Bowden
-
依托单位:
Augmentation of Locomotor Adaptation Post-Stroke
-
批准号:9261392
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2013
-
负责人:Mark G. Bowden
-
依托单位:
Augmentation of Locomotor Adaptation Post-Stroke
-
批准号:8984307
-
项目类别:
-
资助金额:$0.0万
-
财政年份:2013
-
负责人:Mark G. Bowden
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
-
批准号:JCZRQN202500010
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
-
批准号:2025JJ70209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
-
批准号:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
-
批准号:2023JJ50274
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
-
批准号:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
-
批准号:81973577
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
-
批准号:81602908
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: