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临床试验/NCT02850042
NCT02850042已完成2 期

Comparing Constraint-Induced Therapy and Occupation-Based Intervention for Optimal Stroke Recovery

Lumy Sawaki0 个研究点目标入组 16 人开始时间: 2013年6月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
16
主要终点
Fugl Meyer Assessment (FMA

研究概览

简要总结

This pilot study was designed to compare the effects of modified constraint-Induced therapy and occupation-based intervention to increase functional motor recovery in stroke

详细描述

The purpose of this study is to investigate change in motor performance and the extent of neuroplastic change associated with both occupation-based intervention and modified constraint-Induced therapy (m-CIT) in the recovery of upper extremity motor function following a stroke. Transcranial Magnetic Imaging (TMS) will be used to compare the difference in the brain reorganization of each client before and after the intervention to identify which technique is more effective in changing brain function. Central Hypothesis: Stroke subjects with motor deficit receiving occupation-based interventions will demonstrate improved motor function greater to that of the subjects receiving m-CIT interventions. Sixteen participants with chronic stroke will be recruited for the study over the age 21. Participants will be randomly assigned to one of the two therapy groups and will receive 55 minutes of therapy 2 times per week for 4 weeks for a total of 8 sessions.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •21 years of age and older
  • •at least 12 months from stroke
  • •mild-to-severe upper extremity motor deficit
  • •single ischemic or hemorrhagic stroke

排除标准

  • •history of head injury with loss of consciousness
  • •severe alcohol or drug abuse
  • •psychiatric illness interfering with participation in the study including uncontrolled depression
  • •cognitive deficits severe enough to preclude informed consent
  • •ferromagnetic material near the brain
  • •individuals that could be pregnant
  • •cardiac or neural pacemakers
  • •if currently receiving occupational therapy services

研究组 & 干预措施

Occupation-based practice

Experimental

Occupation-based intervention (OBP) is a form of activity-based therapy consisting of client-directed occupations that match client-identified goals. OBP group will participate in activities such as wood working, scrap booking, higher level dressing (don/doffing a bra, zipping coat), hair care, opening doors, using bathroom stalls, typing, cooking, tying shoes, washing dishes, carrying dirty dish carts, clearing dirty dishes and raking. Repetition of the tasks are not the focus in the OBP group. Each session lasted 55-minute and it was delivered twice a week for 4 weeks (8 sessions).

干预措施: Occupation-based practice (OBP) (Behavioral)

Modified-constraint induced therapy

Active Comparator

Modified-constraint induced therapy (m-CIT) group will target functional goals (eg, activities of daily living) or goal subcomponents (eg, pinching, grasp/release, or functional reach patterns). Tasks were repeated at rate of approximately 10 to 50 repetitions each session according to the demands of the task. No physical constraint of the less-affected UE will be applied, but training compelled highly repetitive use of the more-affected upper extremity. Subjects will attempt tasks with progressive difficulty. Each session lasted 55-minute and it was delivered twice a week for 4 weeks (8 sessions).

干预措施: Modified-constraint induced therapy (m-CIT) (Behavioral)

结局指标

主要结局

Fugl Meyer Assessment (FMA

时间窗: Score change after 8 days of intervention compared to baseline

次要结局

  • Canadian Occupational Performance Measure (COPM)(Score change after 8 days of intervention compared to baseline)
  • Stroke Impact Scale (SIS)(Score change after 8 days of intervention compared to baseline)
  • Goal Attainment Scale (GAS).(Score change after 8 days of intervention compared to baseline)
  • Transcranial Magnetic Stimulation (map volume)(Score change after 8 days of intervention compared to baseline)

研究者

发起方
Lumy Sawaki
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Lumy Sawaki

Associate Professor,department of Physical Medicine and Rehabilitation

University of Kentucky

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