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SoCal Savvy: Testing Savvy Caregiver in a Racially and Ethnically Diverse Sample in Southern California

Not Applicable
Completed
Conditions
Caregiver Burnout
Psychological Distress
Interventions
Behavioral: Group sessions over 6 weeks
Behavioral: Group sessions over 3 weeks
Registration Number
NCT04421729
Lead Sponsor
University of Southern California
Brief Summary

The investigators will conduct a hybrid efficacy-effectiveness trial intended to address these gaps by testing the efficacy-effectiveness of two multi-family group interventions, and on 250 English-speaking adults: Savvy Caregiver Express™ (3-session, newly piloted in Los Angeles County for feasibility) and Savvy Caregiver Program (original 6-session evidenced-based intervention), across post-intervention, 3- and 6-months.

Detailed Description

A number of epidemiological studies, systematic reviews, and consensus reports highlight the importance of non-pharmacological, sociobehavioural interventions to address the health, psychological, and social effects of caregiving for persons living with dementia, and the need for tangible information and resources.

The investigators will conduct a hybrid efficacy-effectiveness trial intended to address these gaps by testing the efficacy-effectiveness of two multi-family group interventions, and on 250 English-speaking adults: Savvy Caregiver Express™ (3-session, newly piloted in Los Angeles County for feasibility) and Savvy Caregiver Program (original 6-session evidenced-based intervention), across post-intervention, 3- and 6-months. It is hypothesized that no differences (comparable effects) between the programs in their efficacy/effectiveness and moderating conditions.

Focus groups (\~25 participants) will be conducted to ascertain program acceptability and satisfaction.

The analyses will include a multiple linear mixed-effects modeling for our trial outcomes, and thematic analyses for our focus group interview data.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
121
Inclusion Criteria
  • English- speaking women and men age 18 or older who care for or provide assistance to someone with dementia
Exclusion Criteria
  • Caregivers who have sensory or physical conditions that interfere with participation in an on-site, group-administered activity

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Savvy Caregiver ProgramGroup sessions over 6 weeksSavvy Caregiver Program, 6 weekly sessions, group treatment, addressing educational, informational, and psychosocial issues and community resources.
Savvy ExpressGroup sessions over 3 weeksSavvy Express, 3 weekly sessions, group treatment, addressing educational, informational, and psychosocial issues and community resources.
Primary Outcome Measures
NameTimeMethod
Revised Memory and Behavior Problems Checklist (RMBPC)up to 7 months

caregiver reactivity to family member's memory/behavior problems

Patient Health Questionnaire-9 (PHQ-9)up to 7 months

caregiver depressive symptoms

Generalized Anxiety Disorder (GAD-7)up to 7 months

caregiver anxiety symptoms

Secondary Outcome Measures
NameTimeMethod
Medical Outcomes Study Social Support Survey (MOS)up to 7 months

Measures caregiver social support using the MOS scale

Intent to Institutionalizeup to 7 months

TA one-item measure that assesses if the caregiver intends to institutionalize the family member in the next 6 months

Caregiver Competence Scalesup to 7 months

measures caregiver skills, mastery, competence, management of the situation based on the Caregiver Competence, Management and Meaning Scales

Family Members Activities of Daily Living (ADL)up to 7 months

measures family member's activities of daily living using the Katz ADL scale

Family Members Instrumental Activities of Daily Living (IADL)up to 7 months

measures family member's activities of daily living using the Lawton IDL scale

Trial Locations

Locations (1)

University of Southern California

🇺🇸

Los Angeles, California, United States

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