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N/A N=461 Randomized Double-blind Supportive Care

A Family-centered Intervention for Acutely-ill Persons With Dementia

Alzheimer Disease

Enrolled (actual)
461
Serious AEs
0.0%
Results posted
Jun 2024
Primary outcome: Primary: Return to Baseline Physical Function Based on the Barthel Index (Change From 2 Weeks Prior to Admission and Changes at Admission, Discharge, and 2 and 6 Months Post-discharge). — 0.68; 0.76; 0.77; 0.73 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Family-centered Function-focused Care (Fam-FFC) (Behavioral)
Age
Older Adult · 65+ yrs
Sex
All
Sponsor
Penn State University
Primary completion
Feb 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Return to Baseline Physical Function Based on the Barthel Index (Change From 2 Weeks Prior to Admission and Changes at Admission, Discharge, and 2 and 6 Months Post-discharge).
0.68; 0.76; 0.77; 0.73; 0.77; 0.61
PRIMARY
Caregiver Preparedness
23.7; 23.9; 24.1; 25.0; 26.5; 26.2
SECONDARY
Delirium Severity
1.6; 1.3; 1.0; 1.0; .98; 1.0
SECONDARY
Behavior
8.4; 7.2; 6.5; 6.3; 5.3; 5.4
SECONDARY
Moderate Physical Activity Level
4.8; 8.3; 14.2; 19.1; 23.3; 29.9
SECONDARY
Depression
9.4; 9.0; 7.5; 7.4; 6.2; 6.6
SECONDARY
Caregiver Strain
8.1; 7.9; 8.1; 7.2; 6.9; 6.5
SECONDARY
Caregiver Burden
10.0; 9.7; 13.5; 12.7; 9.0; 7.7
SECONDARY
Caregiver Anxiety
5.4; 5.2; 4.7; 4.5; 4.7; 4.3
SECONDARY
Falls
.15; .14; .52; .41; .76; .57
SECONDARY
Hospitalizations
.05; .10; .33; .41; .32; .33
SECONDARY
Emergency Room (ER) Visits
.06; .08; .41; .44; .46; .35

Summary

This study will address the effectiveness of Family-centered Function Focused Care (Fam-FFC). Fam-FFC is a theoretically-based approach to care in which family caregivers partner with nurses to prevent functional decline and other complications related to hospitalization in older adults with Alzheimer's disease and related dementias. A systematic care pathway promotes information-sharing and decision-making that promotes physical activity, function, and cognitive stimulation during the hospitalization and immediate post-acute period. Our goal in this work is to establish a practical and effective way to optimize function and physical activity; decrease neuropsychiatric symptoms, delirium, and depression; prevent avoidable post-acute care dependency; and prevent unnecessary rehospitalizations and long-stay nursing home admissions, while mitigating family caregiver strain and burden.

Eligibility Criteria

Patient Inclusion Criteria: medical patients who: are age ≥65, speak English or Spanish, live in the community prior to admission to the hospital, screen positive for dementia on well-validated scales (Montreal Cognitive Assessment {MoCA} ≤ 25 123-127 and AD8 >2 128,129), and score 0.5 to 2.0 on the Clinical Dementia Rating Scale; and have a family CG as the designated study partner for the duration of the study. Patient Exclusion Criteria: mild cognitive impairment (CDR 0.5 without functional or ADL impairments), severe dementia (CDR 3), any significant neurological condition associated with cognitive impairment other than dementia (e.g. brain tumor), a major acute psychiatric disorder, have no family caregiver to participate, are enrolled in hospice and/or have a life expectancy of six months or less, are admitted from a nursing home, or experience transfers to another unit for stays longer than 48 hours. Family Inclusion Criteria: age 18 and above whose relatives meet inclusion criteria will be eligible if they can speak and read English or Spanish; and are related to the patient by blood, marriage, adoption, or affinity as a significant other (defined as or by the patient/legally authorized person as the primary person providing oversight and support on an ongoing basis); participate, at a minimum, in the initial assessment and development of FamPath; and able to recall at least two words on the MiniCog Staff nurses (at the conclusion of the intervention at each site) who identify the intervention unit as the primary unit worked, and speak English or Spanish, will be included in focus groups For the exploratory aim of assessing the cultural appropriateness of the intervention, we will recruit family caregivers who self-identify as black, Latino, Asian and white, randomly selected from the Fam-FFC sample. Approximately 10 percent of families from each ethnic group represented in the study will be approached for consent for participation in interviews. (If theoretical saturation is not reached, interviews will continue until saturation is reached). Additionally, the six nurse champions will be consented and interviewed after the study ends in his/her particular unit/setting to provide their perspective on the cultural appropriateness of Fam-FFC.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03046121). 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.

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