Online support program for caregivers of dementia patients
Support Via Technology: Living and Learning With Advancing Dementia-REVISED
This study is testing an online program to see if it can help caregivers of dementia patients feel less stressed and better manage difficult behaviors.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 238 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Oregon Health and Science University Academic / other |
| Locations | 1 site (Portland, Oregon) |
| Trial ID | NCT06460012 on ClinicalTrials.gov |
What this trial studies
The STELLA-R program is an online intervention designed to help caregivers manage the behavioral and psychological symptoms associated with dementia. It employs a cognitive behavioral approach, teaching caregivers to analyze and respond to distressing behaviors of their care recipients. By addressing the common challenges faced by caregivers, the program aims to reduce caregiver burden and improve their overall well-being. Participants will engage in a self-directed curriculum that is accessible from home, minimizing barriers to participation.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 or older who are caregivers for family members with Alzheimer's disease or related dementias and can identify distressing behavioral symptoms.
Not a fit: Patients who may not benefit include those with severe vision problems that prevent participation or those unable to follow study instructions.
Why it matters
Potential benefit: If successful, this program could significantly alleviate the stress and health risks faced by caregivers of individuals with dementia.
How similar studies have performed: Other studies have shown success with similar online interventions aimed at supporting caregivers, indicating a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult caring for family member with ADRD * Age of 18 years or older * Speaks and understands English to be able to participate in intervention * Owns a telephone (smartphone, cell phone or landline) * Has email and mailing address to receive study materials and surveys * Provides informed consent to participate in the research * Lives in Oregon, Washington or Idaho * Identifies two or more behavioral symptoms that are distressing to them (care partner) Exclusion Criteria: * Vision problems severe enough to prevent participation * Unwilling or unable to adequately follow study instructions and participate in study procedures
Where this trial is running
Portland, Oregon
- Oregon Health & Science University, Layton Aging and Alzheimer's Disease Research Center — Portland, Oregon, United States (Recruiting)
Study contacts
- Principal investigator: Allison Lindauer, PhD — Oregon Health and Science University
- Study coordinator: Allison Lindauer, PhD
- Email: lindauer@ohsu.edu
- Phone: (503) 449-8151
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.