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NCT06341777Completed

Multisensory Telerehabilitation for Visual Field Defects

Telerehabilitation for Visual Field Defects: Clinical Efficacy of a Novel Multisensory Therapy for Adults and Children With Acquired Brain Lesions

Source: ClinicalTrials.gov · Last updated 2 Apr 2024

Brief summary (registry, in English)

Brain injuries may cause the loss of the ability to see portions of the visual field, the so-called visual field defects (VFDs). VFDs significantly impact the survivors' functional recovery and quality of life, with the majority of patients displaying no spontaneous recovery or being left with residual deficits. Among the available therapies for VFDs, the compensatory scanning training is considered the most promising. Yet, current evidence is insufficient to recommend it in clinical practice, and the scientific community has stressed the need of more high-quality research. The present randomized clinical trial in patients with chronic VFDs caused by brain lesions aims at verifying the feasibility and efficacy of a novel telerehabilitation using a multisensory scanning therapy, by measuring its effects on visual functions and daily activities, and by looking for neural indicators of the therapy-induced improvements.

Status (registry)
Completed
Study type
Interventional
Enrollment
72 (actual)
First submitted
19 Mar 2024
Start date
1 Jan 2020
Primary completion date
31 Dec 2023
Lead sponsor
Istituto Auxologico Italiano
Diseases
Stroke
NCT number
NCT06341777

What you commit to

  • Study type: Interventional
  • Participants enrolled: 72
  • From 1 Jan 2020 to the primary completion date, 31 Dec 2023
  • 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

  • being enrolled in another therapy for HVFDs
    • not being enrolled in another VFDs therapy.

Other illness

  • major neurological or psychiatric disease

Other

  • cognitive decline (adults)
  • intellectual disability (children)

Who the study is looking for

  • Acquired homonymous visual field defect (HVFDs) due stroke, traumatic brain injury, tumor, surgery for epilepsy in a chronic stage of illness (time from the lesion \>6 months)
  • Normal hearing
  • Normal or corrected-to-normal visual acuity

Age in the registry: 6 years to 70 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
Istituto Auxologico Italiano IRCCS
Coordinator of this site? Confirm its status
MilanItalyUnknown status

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