ACTIVE_NOT_RECRUITING

Dynamic Neural Systems Underlying Social-emotional Functions in Older Adults

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

Assess the impact of a remote, app-delivered digital meditation intervention on emotional well-being of lonely older adults. Neuroimaging, electrophysiological (EEG), and autonomic physiology will be used to assess the neural correlates of the intervention. EEG and autonomic physiology will be collected while participants watch 30 min of an awe-inspiring movie. fMRI and autonomic physiology will be collected in the context of a social exploration/exploitation task.

Official Title

Dynamic Neural Systems Underlying Social-emotional Functions in Older Adults

Quick Facts

Study Start:2023-10-13
Study Completion:2026-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05645835

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 120 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 60 years of age or older
  2. * English language fluency
  3. * Naive to meditation practices (not actively meditating more than one hour per month and/or meditation practice for less than a year in their entire life-time)
  4. * No MRI contra-indications
  5. * Cognitively healthy (no diagnosis of dementia, stroke, developmental disorders, or major systemic diseases that may impact cognitive function)
  1. * Below 60 years of age
  2. * Not fluent in English
  3. * Active meditator (meditating more than one hour per month and/or meditation practice for more than a year in their entire life-time).
  4. * Presence of a severe psychiatric (e.g. schizophrenia, bipolar disorder, PTSD), neurological (epilepsy, traumatic brain injury, dementia, multiple sclerosis), or developmental disorder (e.g. autism)
  5. * Systemic disease (e.g. major recent surgeries, cancer)
  6. * Claustrophobia
  7. * Contraindications for MR safety (e.g. metal in body, cochlea implants)

Contacts and Locations

Principal Investigator

Lorenzo Pasquini, PhD
PRINCIPAL_INVESTIGATOR
University of California, San Francisco

Study Locations (Sites)

University of California San Francisco
San Francisco, California, 94158
United States

Collaborators and Investigators

Sponsor: University of California, San Francisco

  • Lorenzo Pasquini, 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 Date2023-10-13
Study Completion Date2026-07-01

Study Record Updates

Study Start Date2023-10-13
Study Completion Date2026-07-01

Terms related to this study

Additional Relevant MeSH Terms

  • Loneliness
  • Older Adults
  • fMRI
  • Emotions
  • EEG
  • Digital Intervention
  • Meditation