RECRUITING

Patient-Centered NeuroRehabilitation (PCN)

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

As individuals grow older, a number of factors can reduce our cognitive (or thinking) abilities such as "normal" aging, neurodegenerative diseases, and cardiovascular disease. This study will evaluate whether cognitive rehabilitation and transcranial electrical stimulation (TES) can improve cognitive abilities. Cognitive rehabilitation refers to methods that are used to improve tasks people have trouble doing in everyday life. Transcranial electrical stimulation uses small amounts of electricity to try to alter brain functioning. These approaches may help improve cognitive abilities like attention, learning, memory, finding words, and problem solving as well as everyday functioning. The goal of this study is to identify how to best use these methods, either alone or in combination.

Official Title

Patient-Centered NeuroRehabilitation

Quick Facts

Study Start:2016-06
Study Completion:2026-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03036319

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:50 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Individuals who have reported cognitive dysfunction and cognitively intact participants.
  2. 2. Participants will be age 50 or older
  1. 1. A history of epilepsy
  2. 2. Sensory or motor impairments that limit the ability to take part in the study
  3. 3. Current alcohol or drug abuse/dependence
  4. 4. Those who are currently pregnant or may become pregnant during the duration of the study (if there is a question of pregnancy, pregnancy tests will be available for participants at no charge)

Contacts and Locations

Study Contact

Kayla Rinna, M.S.
CONTACT
734-936-7739
krinna@med.umich.edu
Eileen Robinson, RN, MPH
CONTACT
734-763-1356
robinsoe@med.umich.edu

Principal Investigator

Benjamin M Hampstead, Ph.D.
PRINCIPAL_INVESTIGATOR
University of Michigan

Study Locations (Sites)

University of Michigan - Department of Psychiatry
Ann Arbor, Michigan, 48109
United States

Collaborators and Investigators

Sponsor: University of Michigan

  • Benjamin M Hampstead, Ph.D., PRINCIPAL_INVESTIGATOR, University of Michigan

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 Date2016-06
Study Completion Date2026-04

Study Record Updates

Study Start Date2016-06
Study Completion Date2026-04

Terms related to this study

Additional Relevant MeSH Terms

  • Cognitive Deficit