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NCT07646522RecruitingPhase 2

Telerehabilitation and Biomarkers of Recovery After Stroke in Brazil

Telerehabilitation and Biomarkers of Functional Recovery After Stroke in Brazil: TR-BR-1 Clinical Trial

Source: ClinicalTrials.gov · Last updated 16 Jun 2026

Brief summary (registry, in English)

The purpose of this research study is to provide preliminary evidence of whether telerehabilitation targeting arm movement, when added to usual care, improves arm function and reduces global disability after stroke, compared to usual care alone in Brazil. Evaluate the safety and feasibility of telerehabilitation in the Brazilian context. Explore the clinical, neuroimaging, neurophysiological, and economic factors that influence telerehabilitation efficacy in functional recovery following stroke.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
20 (estimated)
First submitted
24 May 2026
Start date
Jun 2026
Primary completion date
Sept 2027
Lead sponsor
University of Sao Paulo
Diseases
Stroke
NCT number
NCT07646522

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 20
  • From Jun 2026 to the primary completion date, Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Unable or unwilling to perform study procedures/therapy, or expectation of noncompliance with study procedures/therapy, or expectation that subject cannot participate in all study visits.
  • Modified Rankin Scale score \>2 prior to the index stroke.
  • A new symptomatic stroke has occurred since the index stroke, or a separate stroke occurred within 30 days prior to the index stroke.
  • Botulinum toxin to the paretic arm: received in the prior 3 months or expected by the 1-Month Visit.
  • Concurrent enrollment in another therapy-based investigational study where the duration of the investigational therapy's activity is likely to occur during the subject's participation in the study.
  • Expectation that participant will not have a single domicile address during the 6 weeks of therapy.

Other illness

  • A major, active, coexistent neurological, psychiatric, or medical disease that reduces the likelihood that a subject will be able to comply with all study procedures.
  • A diagnosis (apart from the index stroke) that substantially affects paretic arm function.
  • Significant cognitive impairment, defined as Montreal Cognitive Assessment \[a lower score can be permitted at the discretion of the PI\].
  • On isolation precautions, e.g., due to active COVID-19.

Other

  • Severe depression, defined as Geriatric Depression Scale Score \>10/15 at Baseline Visit.
  • Deficits in communication that interfere with reasonable study participation.
  • Severe UE spasticity, defined as presence of contracture or modified Ashworth Scale score=4 in either biceps or pectoralis.
  • Lacking visual acuity, with or without corrective lens, of 20/50 or better in at least one eye.
  • Life expectancy \< 9 months
  • Pregnancy; women of child-bearing potential must have a negative pregnancy test.
  • Subject lacks sufficient Portuguese to comply with study procedures and TR instructions.
  • Contraindication to MRI.
  • Contraindication to TMS.
  • Box and Block Test score of ≥30 blocks with the unaffected arm within 60 seconds at Baseline Visit;
  • Spatial neglect interfering with reasonable participation in the study;
  • Distance from the participant's home to the study site greater than 120 km \[this can be waived at the discretion of the PI\].
    • 22\. Availability of a 2 m² space for a table and chair setup.

Who the study is looking for

  • Age 18-80 years at the time of randomization.
  • The index stroke was radiologically verified, due to ischemia, and had time of onset 120±30 days prior to randomization.
  • The stroke caused upper extremity deficits as defined by Action Research.
  • Arm Test score 18-44 (out of 57) at Baseline Visit.
  • Box \& Block Test score with affected arm is ≥1 block in 60 seconds at Baseline Visit.
  • Able to successfully perform all 3 rehabilitation exercise test examples (simple commands) at Baseline Visit.
  • Informed consent and behavioral contract signed by the subject (i.e., no surrogate consent).

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ribeirão Preto Medical School University of São Paulo
Coordinator of this site? Confirm its status
Ribeirão PretoBrazilRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.