N/A N=60 Supportive Care

Producing a Fully Asynchronous Online Savvy Program

Dementia

Bottom Line

View on ClinicalTrials.gov: NCT04951037 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Apr 2024

Primary outcome: Primary: Center for Epidemiologic Studies - Depression (CES-D) Score — 11.483; 9.345; 8.964; 14.317 score on a scale

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Fully Asynchronous Online Savvy Program (Behavioral)
Age: Adult, Older Adult · 18+ yrs
Sex: All
Sponsor: Emory University
Primary completion: Sep 2022

Outcome Measures

Outcome	Result	p-value
PRIMARY Center for Epidemiologic Studies - Depression (CES-D) Score	11.483; 9.345; 8.964; 14.317; 10.848; 10.132	—
PRIMARY Zarit Burden Interview Score	31.207; 29.138; 26.296; 35.050; 31.239; 28.730	—
PRIMARY State-Trait Anxiety Inventory (STAI) Score	31.793; 31.793; 29.893; 34.862; 31.761; 31.103	—
PRIMARY Caregiver Mastery Scale - Caregiving Competence Score	12.160; 12.821; 13.143; 11.481; 12.689; 13.026	—
PRIMARY Revised Memory and Behavior Problem Checklist (RMBPC) Frequency Score	40.276; 36.345; 34.786; 40.407; 35.739; 34.897	—
PRIMARY Revised Memory and Behavior Problem Checklist (RMBPC) Reaction Score	18.483; 12.828; 12.893; 20.167; 12.522; 13.132	—

Summary

This is a pilot/feasibility study to develop and test a fully online, self-administered psychoeducation program to enhance the caregiving mastery of family and friends who provide unpaid care for persons living with Alzheimer's and similar dementia disorders (PLWD).

Eligibility Criteria

Inclusion Criteria

primary unpaid caregiver for a community-dwelling PLWD
provide at least 10 hours of direct care per week
able to read and understand English
be able to access the course online
naïve to Savvy or Tele-Savvy

Exclusion Criteria

cannot provide consent
prisoners
cognitively impaired adult
not able to clearly understand English

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04951037). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.