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临床试验/NCT01738581
NCT01738581已完成1 期

Effectiveness of rTMS and Retraining in the Treatment of Focal Hand Dystonia

University of Minnesota4 个研究点 分布在 1 个国家目标入组 9 人开始时间: 2011年11月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
9
试验地点
4
主要终点
Change From Baseline in Global Rating of Change at Posttest (Day 5)

研究概览

简要总结

This study is exploring a new experimental procedure in dystonia called repetitive transcranial magnetic brain stimulation (TMS) combined with rehabilitation. The purpose of the study is to determine whether repetitive TMS is effective as a treatment to reduce symptoms in dystonia as demonstrated by improved motor performance.

详细描述

BACKGROUND: Though the etiology of focal hand dystonia (FHD) is uncertain, two primary factors implicated in the development of dystonic symptoms are excessive cortical excitability and impaired sensorimotor processing.

OBJECTIVE

The purpose of this study was to determine the functional efficacy and neural effects of a Dual intervention of rTMS and sensorimotor retraining. Our working hypothesis is: subjects receiving the combined intervention will (1) display significantly improved handwriting measures; (2) report significant improvement in daily functional ability; (3) display reduced hand cramping compared; and (4) demonstrate reduced corticospinal excitability after the Dual intervention when compared to the rTMS+ stretching and massage (Sham) intervention.

METHODS: A randomized, single-subject, multiple baseline design with crossover is used for this study that will examine ten subjects with FHD with two interventions: five days of low-frequency 1 Hz rTMS + sensorimotor retraining (Dual intervention) vs. rTMS + stretching and massage (Sham). The rTMS is applied to the premotor cortex at 1 Hz at 90% resting motor threshold for 1200 pulses. For sensorimotor retraining, a subset of the Learning-based Sensorimotor Training program was followed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Greater than 18 years of age
  • Symptoms of focal hand dystonia or writer's cramp

排除标准

  • History of seizure or other neurologic disorder

结局指标

主要结局

Change From Baseline in Global Rating of Change at Posttest (Day 5)

时间窗: Baseline and Posttest

Symptom severity was assessed using the global rating of change (GROC). For the GROC, participants were asked to identify between one to three functions most impacted by focal hand dystonia. At posttest 1 they were then asked to select a rating of perceived change that represented the level of function compared to baseline. Perceived change consisted of a ±7 point Likert scale (+7= a very great deal better, 0= no change, -7= a very great deal worse).

次要结局

  • Change From Baseline in Sensation at Posttest (Day 5)(Baseline and Posttest)
  • Change From Baseline in Cortical Silent Period at Posttest (Day 5)(Baseline and Posttest)
  • Change From Baseline in Arm Dystonia Disability Scale at Posttest (Day 5)(Baseline and Posttest)
  • Change From Baseline in Physical Function at Posttest (Day 5)(Baseline and Posttest)
  • Change From Baseline for Pressure During Hand Writing at Posttest (Day 5)(Baseline and Posttest)
  • Change From Baseline for Physician Rated Impairment at Posttest (Day 5)(Baseline and Posttest)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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