RECRUITING

Lifestyle Interventions for the Treatment of Early Onset Alzheimer's Disease Study

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Conditions

Alzheimer Disease, Early Onsetlifestyle interventioncognitive trainingexercise trainingcognition

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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

The purpose of this study is to generate preliminary data on the benefit of computerized cognitive training and Tai Chi- Qi Gong training in participants with Early-Onset Alzheimer's Disease. It is hypothesized that participants in the experimental training condition will perform better on outcomes related to cognition, functioning, and mood at follow-up compared to participants assigned to the active control condition.

Official Title

Lifestyle Interventions for the Treatment of Early Onset Alzheimer's Disease Study

Quick Facts

Study Start:2024-01-11
Study Completion:2028-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05573490

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:40 Years to 75 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Enrolled in the Longitudinal Early-Onset AD Study (LEADS) parent study, and being classified via LEADS consensus criteria as having amyloid-positive Early Onset Alzheimer's Disease
  2. * Aged 40-64 years at the time of enrollment into LEADS
  3. * Fluent in English
  4. * In good general health and absent another neurological disorder
  5. * Have a knowledgeable informant.
  6. * Have had a Clinical Dementia Rating scale of 0.5 to 1.0 at the time of enrollment into LEADS
  7. * Have sufficient vision, hearing, comprehension, and manual dexterity to participate in the testing and training program
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Dustin B Hammers, PhD
CONTACT
3179638557
hammersd@iu.edu

Principal Investigator

Dustin B Hammers, PhD
PRINCIPAL_INVESTIGATOR
Indiana University

Study Locations (Sites)

Indiana University
Indianapolis, Indiana, 46202
United States

Collaborators and Investigators

Sponsor: Indiana University

  • Dustin B Hammers, PhD, PRINCIPAL_INVESTIGATOR, Indiana University

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 Date2024-01-11
Study Completion Date2028-06

Study Record Updates

Study Start Date2024-01-11
Study Completion Date2028-06

Terms related to this study

Keywords Provided by Researchers

  • lifestyle intervention
  • cognitive training
  • exercise training
  • cognition

Additional Relevant MeSH Terms

  • Alzheimer Disease, Early Onset