RECRUITING

The Rapid Diagnosis of MCI and Depression in Patients Ages 60 and Over

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

Mild cognitive impairment (MCI) leading to Alzheimer's disease and related disorders (ADRD) represents a significant health and economic burden of the rapidly expanding senior population. The accurate detection and diagnosis of MCI and its common comorbidity, late-life depression (LLD), is essential for prolonging patient quality of life and developing advancements in research and treatment options. The purpose of the proposed program is to refine Miro Health's A.I. to accurately detect, differentiate and diagnose MCI and LLD.

Official Title

The Proactive Screening and Diagnosis of Mild Cognitive Impairment and Depression in Patients Ages 60 and Over: An Implementation Study

Quick Facts

Study Start:2023-09-08
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06011681

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:60 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * LLD: Age 60 or over; diagnosis of LLD or symptoms consonant with LLD; PHQ-9 score from 15 to 27
  2. * MCI: Age 60 or over; diagnosis of MCI or self-reported insidious onset and continued worsening of cognitive decline; intact activities of daily living
  3. * HC: Age 60 or over
  1. * Age 59 or younger; history of unresolved neurological or psychiatric conditions; current medications known to affect cognition; history of substance abuse; unable to perform activities of daily living; change in employment status due to condition

Contacts and Locations

Study Contact

Shenly Glenn
CONTACT
415-300-0533
shenly@mirohealth.com
J o e l M e f f o r d, PHD
CONTACT
5 1 0 - 2 9 2 - 8 0 1 7
j o e l @ m i r o h e a l t h . c o m

Principal Investigator

Shenly Glenn, BS
PRINCIPAL_INVESTIGATOR
Miro Health

Study Locations (Sites)

Miro Health
Sacramento, California, 95816
United States
Miro Health
Miami, Florida, 33070
United States

Collaborators and Investigators

Sponsor: Miro Health

  • Shenly Glenn, BS, PRINCIPAL_INVESTIGATOR, Miro Health

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 Date2023-09-08
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2023-09-08
Study Completion Date2024-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Depression
  • Mild Cognitive Impairment