RECRUITING

Gut Microbiome and Blood Indices in Patients With AD and Their Spousal Caregivers

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

Spousal caregivers of Alzheimer's Dementia (AD) patients have an elevated risk of developing AD in the future. Past studies have shown the presence of serum indicators correlated with gut biome dysfunction in AD patients. We hypothesize that the same gut biome dysfunction may be present in spousal caregivers of AD patients.

Official Title

Gut Microbiome and Blood Indices in Patients With AD and Their Spousal Caregivers

Quick Facts

Study Start:2022-12-15
Study Completion:2024-11-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05601856

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:65 Years to 90 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. patients with AD whose clinical dementia rating (CDR) is \> 1
  2. 2. Spouses of Patients in the above group Or
  3. 3. Healthy adult unrelated to groups 1 and 2, with no history of dementia And
  4. 4. Regardless of the grouping, the prospective subject must be between 65 and 90 years old
  1. 1. Familial Alzheimer's Disease (AD)
  2. 2. Severe cardiovascular disease
  3. 3. Severe respiratory system disease
  4. 4. Severe liver disease
  5. 5. Severe kidney disease
  6. 6. Severe central nervous system diseases
  7. 7. Having a lifespan of fewer than 3 months
  8. 8. History of psychiatric illness
  9. 9. Major neurological diseases other than AD
  10. 10. Current use of corticosteroids, antibiotics, or bowel motility modification agents
  11. 11. Any history of Alcoholism or illicit drug dependence
  12. 12. Previous inclusion in this study
  13. 13. Difficulty with follow-up or poor compliance
  14. 14. Severe hearing impairment
  15. 15. Severe vision impairment

Contacts and Locations

Study Contact

Keita Ikeda, PHD
CONTACT
9195931174
keita.ikeda@virginia.edu
ZHIYI ZUO, MD PHD
CONTACT
4349824481
zz3c@uvahealth.org

Study Locations (Sites)

University of Virginia
Charlottesville, Virginia, 22908-0710
United States

Collaborators and Investigators

Sponsor: University of Virginia

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 Date2022-12-15
Study Completion Date2024-11-30

Study Record Updates

Study Start Date2022-12-15
Study Completion Date2024-11-30

Terms related to this study

Keywords Provided by Researchers

  • Alzheimers
  • biome

Additional Relevant MeSH Terms

  • Alzheimer Disease
  • Gut Biome