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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04349488
Other study ID # 2016/287
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 16, 2020
Est. completion date June 30, 2020

Study information

Verified date April 2020
Source University of Liege
Contact Stephen Bornheim, Msc
Phone 003243662193
Email stephen.bornheim@uliege.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

16 acute stroke patients will be split into 2 groups. One group will receive the real treatment (anodal tDCS) and one group sham.

Subjects will receive, in addition to conventional rehabilitation, 2mA for 20 mins of their attributed tDCS, 5 times a week.

Evaluations will take place before the first stimulation period (48h post stroke), after 1, 2, 3 and 4 weeks.

The evaluations are the Four Square Step Test, the Berg Balance Scale, the Postural Assessment Scale For Stroke, the Trunk Impairment Scale, the Time Up & Go and the 10 meter walking test.


Recruitment information / eligibility

Status Recruiting
Enrollment 16
Est. completion date June 30, 2020
Est. primary completion date June 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- First Ever Stroke

- Motor or sensory deficit

- Understands and follows orders

- Signed inform consent

Exclusion Criteria:

• One Yes on the medium and high risk sections of the TSST (Bornheim et al.,2019)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Anodal Transcranial Direct Current Stimulation
Subjects received a micro-current through their scalp to induce cortical and subcortical changes

Locations

Country Name City State
Belgium Liege Univeristy Hospital Liege

Sponsors (1)

Lead Sponsor Collaborator
University of Liege

Country where clinical trial is conducted

Belgium, 

References & Publications (1)

Bornheim S, Croisier JL, Maquet P, Kaux JF. Proposal of a New Transcranial Direct Current Stimulation Safety Screening Tool. Am J Phys Med Rehabil. 2019 Jul;98(7):e77-e78. doi: 10.1097/PHM.0000000000001096. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Changes Four Square Step Test The subject is required to sequentially step over four canes set-up in a cross configuration on the ground. The faster the score, the better the patients balance and coordination. Pre Stimulation (48 hours post stroke), Week 1, Week 2, Week 3, Week 4
Primary Changes Berg Balance Scale Balance Test. Minimum score is 0, maximum 36. The higher the score, the better the balance. Pre Stimulation (48 hours post stroke), Week 1, Week 2, Week 3, Week 4
Primary Changes Postural Assessment Scale For Stroke alance Test. Minimum score is 0, maximum 56. The higher the score, the better the balance. Pre Stimulation (48 hours post stroke), Week 1, Week 2, Week 3, Week 4
Primary Changes Trunk Impairment Scale alance Test. Minimum score is 0, maximum 23. The higher the score, the better the balance. Pre Stimulation (48 hours post stroke), Week 1, Week 2, Week 3, Week 4
Primary Changes Time Up & Go To determine fall risk and measure the progress of balance, sit to stand and walking. The faster, the better. Pre Stimulation (48 hours post stroke), Week 1, Week 2, Week 3, Week 4
Primary Changes 10 meter walking test 10 meter walking test, the faster the better Pre Stimulation (48 hours post stroke), Week 1, Week 2, Week 3, Week 4
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