RECRUITING

tDCS for Post-Stroke Cognitive Impairment

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Conditions

StrokeMild Cognitive ImpairmentPost-Stroke cognitive impairment

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study will evaluate the effects of a form of non-invasive brain stimulation on brain functioning and memory in participants with post-stroke cognitive impairment (PSCI).

Official Title

Post-Stroke Cognitive Impairment: Neurovascular Mechanisms and Non-Invasive Brain Stimulation

Quick Facts

Study Start:2024-09-30
Study Completion:2027-06-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06516588

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 99 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. 1. clinically significant or unstable medical or psychiatric condition;
  2. 2. diagnosis of severe depression;
  3. 3. history of relevant neurological diagnosis (e.g., epilepsy);
  4. 4. previous neurosurgical procedure with craniectomy;
  5. 5. contraindications to tDCS (implanted brain medical devices);
  6. 6. severe visual impairment, hearing impairment, aphasia, neglect or dementia.

Contacts and Locations

Study Contact

Cheryl Adams, RN
CONTACT
(405) 271-8130
gerolab@ouhsc.edu
Camila Bonin Pinto, PhD
CONTACT
(405) 271-8130
gerolab@ouhsc.edu

Study Locations (Sites)

University of Oklahoma
Oklahoma City, Oklahoma, 73117
United States

Collaborators and Investigators

Sponsor: University of Oklahoma

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-09-30
Study Completion Date2027-06-30

Study Record Updates

Study Start Date2024-09-30
Study Completion Date2027-06-30

Terms related to this study

Keywords Provided by Researchers

  • Post-Stroke cognitive impairment

Additional Relevant MeSH Terms

  • Stroke
  • Mild Cognitive Impairment