N/A
N=39
VOCALE LBD+ for Caregivers of Persons With Lewy Body Dementia
Caregiver Burden · Lewy Body Disease · Stress · Skill, Coping
Bottom Line
View on ClinicalTrials.gov: NCT05622734 ↗Enrolled (actual)
39
Serious AEs
0.0%
Results posted
Sep 2024
Primary outcome: Primary: Effect Size of Change From Baseline Caregiving Mastery at 4 Weeks — -0.04 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- VOCALE LBD+ (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Washington
- Primary completion
- Nov 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Effect Size of Change From Baseline Caregiving Mastery at 4 Weeks |
-0.04 | — |
Summary
The goal of this clinical trial is to evaluate the feasibility, acceptability, and initial efficacy of the VOCALE LBD+ intervention in caregivers of persons living with Lewy Body Dementia. The main question[s] it aims to answer are:
* What is the extent to which the VOCALE LBD+ intervention affects caregiving mastery scores at the end of the eight-week intervention
* What is the extent to which a change in caregiving mastery scores is retained four weeks after the end of the VOCALE LBD+ intervention
Participants will be asked to participate in a fully online asynchronous VOCALE LBD+ intervention that involves a moderated web-based discussion platform, peer-to-peer support, didactic training, and problem-solving skill enactment.
Eligibility Criteria
Inclusion Criteria
- Informal and/or lay caregiver of a patient with LBD
- Can read, write, and speak English
- Has access to a device that can be used for videoconferencing and/or phone calls
- 18 years or older
Exclusion Criteria
- Not an informal and/or lay caregiver
- Cannot read and write in English
- No access to a device that can be used for videoconferencing and/or phone calls Younger than 18 years old
Data sourced from ClinicalTrials.gov (NCT05622734). 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.