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Transcranial Direct Current Stimulation in Stroke Rehabilitation

The Use of Transcranial Direct Current Stimulation in the Recovery of Postural Control in Stroke

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01356654
Enrollment
34
Registered
2011-05-19
Start date
2010-03-31
Completion date
2011-06-30
Last updated
2011-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

Stroke, TDCS, Gait, Balance, loss of postural balance

Brief summary

This study investigates if transcranial Direct Current Stimulation (tDCS) is effective in the recovery of postural control in stroke rehabilitation.

Detailed description

The patients were divided in 2 groups by a randomisation procedure. All patients participated for 2 months in the study. Group 1 received true tDCS in the first month followed by SHAM stimulation in the second month. Group 2 received SHAM in the first month and true stimulation in the following month. Four stimulations of 20minutes were provided during 4 weeks before before changing stimulation intensity.

Interventions

DEVICEApplication of Transcranial direct current stimulation (TDCS)

Application of TDCS for 20 minutes, 4 times a week for 4 weeks.

DEVICETranscranial Direct current stimulation

Application of true TDCS for 20min, 4 times a week for 4 weeks.

Sponsors

Rehabilitation Hospital Hof Ter Schelde
CollaboratorUNKNOWN
Artesis University College, Antwerp
CollaboratorOTHER
Universiteit Antwerpen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients suffering from the consequences of a stroke in the medial cerebral artery, during the sub-acute phase (4-24 weeks after onset) 2. Age between 18-75 years 3. Hospitalised in rehabilitation Hospital Hof Ter Schelde 4. Capable of understanding and giving informed consent

Exclusion criteria

1. Cerebellum or brainstem lesions 2. Recently multiple lesions and older lesions which are manifested clinically. 3. History of severe substance abuse (alcohol, drugs, benzodiazepines) 4. Cardiac disease that in the opinion of the clinician precludes participation in the trial (severe dyspnea in rest, severe rhythm disturbances, etc) 5. History of epileptic insults, not caused by the stroke 6. Severe organic co morbidity 7. Psychiatric disorders or history of psychiatric disorders 8. Pace maker / internal defibrillator 9. Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Trunk Impairment Scale (reporting a change on trunk performance at baseline, after 1 month and after two months)baseline, after 1 month, After 2 monthsThe static sitting balance subscale assesses whether a subject can sit independently and remain seated when the legs are either passively or actively crossed. The dynamic sitting balance subscale evaluates the ability to actively shorten each side of the trunk, first initiated from the shoulder and subsequently initiated from the pelvic girdle. Trunk coordination is evaluated by the possibility to independently rotate the upper and lower part of the trunk. The scoring range for the static and dynamic sitting balance and coordination subscales are 7, 10 and 6 points respectively.
Rivermead Motor Assessment Battery (RMAB) (reporting a change on motricity of gross function, arm, leg and trunk at baseline, after 1 month and after two months)baseline, after 1 month, After 2 monthsThe RMAB assesses the motor performance of patients with stroke.32 It consists of test items clustered in three sections that are ordered hierarchically. The gross function subscale (13 items), the Leg and Trunk subscale (10 items) and the arm subscale (15 items)
Tinetti Test (reporting a change on balance and gait tasks at baseline, after 1 month and after two months)baseline, after 1 month, After 2 monthsThe Tinetti Test is an easily performed test that measures a patients' gait and balance. The individual scores are combined to form three measures; a gait score, a standing balance score and a total score. The maximum score for the gait component and the balance component are 12 and 16 points respectively, resulting in a maximum of 28 points for the total score.

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026