跳至主要内容
临床试验/NCT05811819
NCT05811819招募中不适用

Reversing Physiological Dysfunction With Non-invasive Brain Stimulation: Physiological Changes From Hand Movement Therapy

IRegained Inc.1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2022年10月19日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
10
试验地点
1
主要终点
ABILHAND- Change is being assessed

研究概览

简要总结

10 participants with upper-limb impairment will be recruited from community sources. They will be invited to participate in a 15-day trial involving the IRegained device. The study will involve 2 assessment visits to McMaster, before and after the treatment, and 15 treatment visits. The data from the pilot study will be analyzed both quantitatively and qualitatively, as outcomes and explicit feedback from participants will be used to further optimize the device for future studies.

详细描述

This pilot study will investigate the potential changes in the brain area controlling hand movement following 15 days of exercises to improve hand function in participants with upper limb impairments resulting from stroke. A device developed by Dr. Vineet Johnson (IRegained Inc.) will be used to administer standardized exercises to improve hand function. To assess brain changes, transcranial magnetic stimulation pulses will be delivered to the motor cortex. The motor evoked potential (MEP), a muscle response evoked from the TMS, will be measured using electrodes on the hand. This study will test the feasibility of conducting motor therapy using this device while assessing potential changes in motor cortex function. Findings from this study will contribute to developing treatment trials aimed at improving impaired limb function in stroke patients and quality of life in these individuals

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Sustained a single stroke >6months prior to start of study

排除标准

  • •Severe spasticity or contractures (2 or less in the CMSA)
  • •any other musculoskeletal or neuromuscular disorders that compromise sensation
  • •Prospective participants who are incapable of providing consent to participate in the research study will also be excluded (determined by an MMSE score of 23 or less).

研究组 & 干预措施

Neurorehabilitation of the Hand

Experimental

Participants will undergo a 1-hour training session 5 days per week, over 3 weeks for a total of 15 sessions. Hand function therapy will be administered using the gamified protocol to enhance rehabilitation of the hand and provide participants with greater opportunity to regain hand function over the course of the study.

干预措施: Treatment using the MyHand System (Device)

结局指标

主要结局

ABILHAND- Change is being assessed

时间窗: Baseline- before beginning the treatment and Post treatment- after the conclusion of 15 treatment sessions, within 5 days

a subjective functional assessment tool will be used. The tool is a 23-item survey, and participants are provided with a list of various everyday functional tasks and are scored based on patient response. For example, participant will be asked whether it is 'easy', 'difficult' or 'impossible' for each of the 23 tasks.

Chedoke Arm and Hand Activity Inventory 9 (CAHAI-9)- Change is being assessed

时间窗: Baseline- before beginning the treatment and Post treatment- after the conclusion of 15 treatment sessions, within 5 days

a 9-item assessment, will be performed by a trained clinician to estimate a participants functional ability during the initial assessment. The CAHAI-9 requires a participant to perform 9 bimanual ADLs, each of which will be scored on a 7 point scale.

Box and Block (BBT)- Change is being assessed

时间窗: Baseline- before beginning the treatment and Post treatment- after the conclusion of 15 treatment sessions, within 5 days

The BBT requires participants to move cubical wooden blocks over a partition from one box to another. Grip and pinch dynamometry will be used to assess a participant's hand strength.

次要结局

  • Grip Dynamometry- Change is being assessed(Baseline- before beginning the treatment and Post treatment- after the conclusion of 15 treatment sessions, within 5 days)
  • Finger Goniometry- Change is being assessed(Baseline- before beginning the treatment and Post treatment- after the conclusion of 15 treatment sessions, within 5 days)
  • Pinch Dynamometry- Change is being assessed(Baseline- before beginning the treatment and Post treatment- after the conclusion of 15 treatment sessions, within 5 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验