RECRUITING

BID WM Digital Intervention in Aging

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 goal of this clinical trial is to learn if engaging with an digital intervention may improve cognitive function. The main questions it aims to answer are: 1. Does engagement in with a digital intervention improve working memory? 2. Does engagement in with a digital intervention improve inhibitory control? Researchers will compare two different digital interventions to assess whether they may be helpful in improving cognitive function. Participants will conduct study activities remotely (e.g., at-home): 1. Baseline Assessment. Complete a series of cognitive assessments and surveys. 2. Intervention. Engage in a digital intervention for up to 8 weeks. 3. Post Intervention Assessment. Complete the same cognitive assessments and surveys as the Baseline Assessment. 4. Follow-Up Assessment. Six months after the intervention ends, participants will complete the same cognitive assessments and surveys as the Baseline Assessment.

Official Title

Behavioral Intervention Development Core - Working Memory Digital Intervention in Aging

Quick Facts

Study Start:2025-08-15
Study Completion:2028-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06918704

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 to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Minimum of 12 years of education
  2. * English fluency
  3. * Normal or corrected-to-normal vision
  4. * Normal or corrected-to-normal vision
  5. * Medically healthy older adults including those with below-average cognitive performance or mild cognitive impairment patients without dementia
  1. * Under the age of 60
  2. * Clinical diagnosis of neurological or psychiatric disorder
  3. * Visually or hearing impaired without correction to normal
  4. * Clinical diagnosis of dementia or AD8 score of \>3
  5. * Regularly (one or more times per week) practicing an instrument within the last year
  6. * 10 or more years of formal musical instrument training

Contacts and Locations

Study Contact

Melissa Arioli
CONTACT
(415) 506-7321
Bid.Core@ucsf.edu

Principal Investigator

Theodore Zanto, PhD
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

University of California, San Francisco
San Francisco, California, 94621
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Theodore Zanto, PhD, PRINCIPAL_INVESTIGATOR, University of California, San Francisco

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 Date2025-08-15
Study Completion Date2028-06

Study Record Updates

Study Start Date2025-08-15
Study Completion Date2028-06

Terms related to this study

Keywords Provided by Researchers

  • Cognitive Training
  • Working Memory
  • Inhibitory Contorl

Additional Relevant MeSH Terms

  • Working Memory
  • Inhibitory Control