RECRUITING

A Dyadic Sleep Health Approach for Persons With Alzheimer's Disease and Caregivers

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

This is a randomized controlled trial over 5 years, using Stage II of the NIH-defined stage model for behavioral intervention development. We will evaluate the efficacy of the sleep intervention program (Care2Sleep) on sleep, health status measures, and quality of life (for dyads), and inflammation (for caregivers only). Eligible participants will be randomly assigned to in-person Care2Sleep, telehealth Care2Sleep, or to an in-person education control group. The Care2Sleep programs and the control education program will consist of five sessions. The intervention and control programs will begin after baseline assessment and randomization. Posttreatment assessments will be performed immediately after the last session and at 6-month follow-up.

Official Title

A Dyadic Approach to Improve Sleep and Well-Being Among Persons With Alzheimer's Disease and Their Caregivers

Quick Facts

Study Start:2022-11-09
Study Completion:2027-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05452031

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. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. * Patients will be excluded if they are bedbound or have severe medical conditions with a life expectancy of less than 6 months.
  2. * Paid, professional caregivers will also be excluded.
  3. * If the eligibility criteria for either a patient or a caregiver are not met, the dyads will be excluded for this study.

Contacts and Locations

Study Contact

Yeonsu Song
CONTACT
310-983-3029
ysong@sonnet.ucla.edu

Study Locations (Sites)

University of California San Diego
La Jolla, California, 92093
United States
University of California Los Angeles
Los Angeles, California, 90095
United States
Veterans Affairs Greater Los Angeles Healthcare System
Los Angeles, California, 91343
United States

Collaborators and Investigators

Sponsor: University of California, Los Angeles

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 Date2022-11-09
Study Completion Date2027-08-31

Study Record Updates

Study Start Date2022-11-09
Study Completion Date2027-08-31

Terms related to this study

Keywords Provided by Researchers

  • Dementia
  • Caregivers

Additional Relevant MeSH Terms

  • Sleep