RECRUITING

Real-life Dual-Task Training

Conditions

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

Older adults have difficulty optimizing two tasks at once and typically experience greater interference than younger adults when dual-tasking, meaningful that there is greater decline in performance of at least one task when comparing single and dual-tasking. Difficulty dual-tasking may actually predict falls in community-dwelling older adults. Dual-task training has been shown to improve cognitive outcomes (attention, memory), motor outcomes (balance, gait), and dual-task performance in older adults; however, most dual-task training involves simulated tasks that do not reflect functional dual tasks in the real world. Greater dual-task improvements could be seen when training functionally specific tasks. One way to increase task specificity is to offer real-life, contextually-relevant, dual-task training embedded in instrumental activities of daily living (IADLs). Limited evidence exists for dual-task training interventions for older adults with T2DM; however there is early evidence of improvements in cognitive and motor effects with simulated dual-task training, which could translate to improved dual-task performance, reduced impact on everyday life, and reduced fall risk. Therefore, the purpose of this study is to assess feasibility, acceptability, and preliminary efficacy of a real-life dual-task training program for older adults at risk to fall.

Official Title

Real-life Dual-Task Training for Older Adults at Risk to Fall

Quick Facts

Study Start:2024-07-03
Study Completion:2026-07-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06479694

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
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * at least 65 years old
  2. * ambulatory around the home with or without an assistive device
  3. * answered yes to at least one of the fall risk questions with their therapist
  4. * scheduled to receive occupational therapy services with instrumental activity of daily living goals through Covell Care.
  1. * Not fluent in English
  2. * Self-reported diagnosis of dementia

Contacts and Locations

Study Contact

Laura A Swink, PhD
CONTACT
9704917915
laura.swink@colostate.edu

Study Locations (Sites)

Colorado State University
Fort Collins, Colorado, 80524
United States

Collaborators and Investigators

Sponsor: Colorado State 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 Date2024-07-03
Study Completion Date2026-07-01

Study Record Updates

Study Start Date2024-07-03
Study Completion Date2026-07-01

Terms related to this study

Additional Relevant MeSH Terms

  • Fall