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RECRUITING
NCT06265766
NA

Brain STimulation for Arm Recovery After Stroke 2

Sponsor: Jord Vink

View on ClinicalTrials.gov

Summary

Rationale: Every year, about 40,000 people in the Netherlands have a stroke. After the initial admission to the hospital, about 15% of stroke survivors is admitted to a rehabilitation center because of remaining disabilities. Three out of four of these patients have upper limb dysfunction, hampering activities of daily living. Upper limb function plays a critical role in the performance of most daily life activities. In our phase II trial B-STARS, continuous theta burst stimulation (cTBS) treatment led to an absolute additional recovery of upper limb function of 17%, as measured with the Action Research Arm Test (ARAT) score three months after stroke. This improvement exceeds the minimal clinically important difference of 10%. cTBS treatment also resulted in a significant improvement in measures of activities and participation (of similar magnitude) and a reduction in the mean length of stay at the rehabilitation center by 18 days. Objective: To assess the effectiveness and cost effectiveness of cTBS treatment in promoting upper limb recovery after stroke in patients admitted to a rehabilitation center. Study design: A phase III, multi-center, double-blind, randomized, sham-controlled, clinical trial. Study population: 454 patients aged 18 years or older with a first-ever ischemic stroke or intracerebral hemorrhage and a unilateral arm paresis, defined by a Motricity Index between 9 and 99, in whom cTBS treatment can be started within 3 weeks after stroke onset. Intervention: 10 daily sessions of cTBS delivered over the contralesional primary motor cortex during a period of 2 weeks, delivered immediately before regular care physical therapy of the affected upper limb. Main study parameters/endpoints: The primary endpoint will be the score on the upper extremity section of the Fugl-Meyer assessment (FM-UE) at 90 days after stroke. Secondary endpoints will include the score on the FM-UE at one year and the scores on the Action Research Arm Test, Nine Hole Peg Test, Stroke Impact Scale, EuroQol 5 Dimensions and modified Rankin Scale at 90 days and one year after stroke

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

454

Start Date

2024-12-09

Completion Date

2029-12-31

Last Updated

2025-08-27

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Active cTBS

10 sessions of active cTBS delivered to the contralesional primary motor cortex, started within 3 weeks after stroke.

DEVICE

Sham cTBS

10 sessions of sham cTBS delivered to the contralesional primary motor cortex, started within 3 weeks after stroke.

Locations (16)

Tolbrug

's-Hertogenbosch, Netherlands

Reade

Amsterdam, Netherlands

Revalidatie Friesland

Beetsterzwaag, Netherlands

Revant

Breda, Netherlands

MRC Aardenburg

Doorn, Netherlands

Libra Blixembosch

Eindhoven, Netherlands

University Medical Center Groningen

Groesbeek, Netherlands

Merem

Hilversum, Netherlands

Adelante

Hoensbroek, Netherlands

Basalt

Leiden, Netherlands

Sint Maartenskliniek

Nijmegen, Netherlands

Basalt

The Hague, Netherlands

Libra Leijpark

Tilburg, Netherlands

De Hoogstraat

Utrecht, Netherlands

Heliomare

Wijk aan Zee, Netherlands

Vogellanden

Zwolle, Netherlands