RECRUITING

Support Via Technology: Living and Learning With Advancing Dementia-REVISED

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

STELLA-R is a multicomponent, self-directed, online intervention designed to facilitate effective management of behavioral and psychological symptoms that are common in many types of dementia. The curriculum instructs care partners to use the ABC approach, a cognitive behavioral technique that teaches care partners to describe a Behavior, then consider the Activators and Consequences of a care recipient behavior. The goal of this intervention is to reduce care partner burden and decrease reactivity to upsetting behaviors.

Official Title

Support Via Technology: Living and Learning With Advancing Dementia-REVISED

Quick Facts

Study Start:2024-07-01
Study Completion:2026-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06460012

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:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult caring for family member with ADRD
  2. * Age of 18 years or older
  3. * Speaks and understands English to be able to participate in intervention
  4. * Owns a telephone (smartphone, cell phone or landline)
  5. * Has email and mailing address to receive study materials and surveys
  6. * Provides informed consent to participate in the research
  7. * Lives in Oregon, Washington or Idaho
  8. * Identifies two or more behavioral symptoms that are distressing to them (care partner)
  1. * Vision problems severe enough to prevent participation
  2. * Unwilling or unable to adequately follow study instructions and participate in study procedures

Contacts and Locations

Study Contact

Allison Lindauer, PhD
CONTACT
(503) 449-8151
lindauer@ohsu.edu
Christina Zonker, BA
CONTACT
(503) 816-8310
zonkerc@ohsu.edu

Principal Investigator

Allison Lindauer, PhD
PRINCIPAL_INVESTIGATOR
Oregon Health and Science University

Study Locations (Sites)

Oregon Health & Science University, Layton Aging and Alzheimer's Disease Research Center
Portland, Oregon, 97239
United States

Collaborators and Investigators

Sponsor: Oregon Health and Science University

  • Allison Lindauer, PhD, PRINCIPAL_INVESTIGATOR, Oregon Health and Science 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 Date2024-07-01
Study Completion Date2026-12-01

Study Record Updates

Study Start Date2024-07-01
Study Completion Date2026-12-01

Terms related to this study

Keywords Provided by Researchers

  • caregivers
  • dementia
  • RMBPC
  • caregiver support

Additional Relevant MeSH Terms

  • Caregiver Burden