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Home Hand Training Over Video for Adults Living With Stroke

Tests remotely guided hand training at home in adults with chronic stroke.

Plain-language title generated from the registry record
Registry title: Telerehabilitation for Post-Stroke Hand Function

Key facts

Where
Ann Arbor, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 40 and 75 years old?

Source: NCT07792655, who can take part

Where in United States

  • Physical Medicine & Rehabilitation 325 E Eisenhower Pkwy Suite 3011Ann Arbor, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Michigan
Trial code
NCT07792655
Record updated
15 October 2026
Original description
This pilot randomized controlled trial will evaluate the feasibility and preliminary effects of a home-based, technology-enabled hand telerehabilitation program for adults with chronic stroke. Participants will receive either remotely guided hand training or a standard home exercise program matched for duration and intensity. Outcomes will include measures of hand function, adherence, and feasibility to assess the potential of telerehabilitation for improving access to structured post-stroke hand rehabilitation.Read full original descriptionShow less

Telerehabilitation for Post-Stroke Hand Function

This pilot randomized controlled trial will evaluate the feasibility and preliminary effects of a home-based, technology-enabled hand telerehabilitation program for adults with chronic stroke. Participants will receive either remotely guided hand training or a standard home exercise program matched for duration and intensity. Outcomes will include measures of hand function, adherence, and feasibility to assess the potential of telerehabilitation for improving access to structured post-stroke hand rehabilitation.

Inclusion: Unilateral cortical or subcortical stroke; Chronic stroke (≥ 6 months since stroke); No significant cognitive deficits as determined by the Mini Mental State Examination (MMSE) score (score≥ 22).

Exclusion: Ferromagnetic metal implants in the skull; Cochlear implant; Previous serious adverse reaction to TMS; Cerebellar stroke; Unstable heart condition, uncontrolled diabetes or hypertension; History of significant orthopedic or neurological conditions that could affect hand function (e.g., multiple sclerosis); Recent history of significant spatial neglect; History of a recent Botulinum Toxin (Botox) injection to the upper-extremity muscles (≤ 3 months); Recent history of repeated fainting spells or syncope; Recent history of seizure while on anti-seizure medication; Recent history of skull fracture/head injury; Skull defect related to the current stroke; Implanted electronic cardiac device (e.g., cardiac pacemaker); Recent trauma or fracture in the upper extremities; Joint contractures or significant spasticity in the hand; Pregnant or actively planning to become pregnant (self-reported); Inability to communicate or unable to consent; Unable to obtain reliable motor evoked potentials; Implanted deep brain stimulator; Implanted vagus nerve stimulator; Implanted cervical spine epidural stimulator; Ventriculoperitoneal shunt.

ClinicalTrials.gov NCT07792655