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The Dementia Symptom Management at Home Program

The Dementia Symptom Management at Home Program: A Bundled Interprofessional Intervention to Improve Dementia Patient-Caregiver Dyad Quality of Care and Quality of Life Through Home Healthcare.

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02482623
Acronym
DSM-H
Enrollment
0
Registered
2015-06-26
Start date
2017-08-01
Completion date
2018-03-01
Last updated
2022-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia

Keywords

Dementia, neuropsychiatric symptoms, implementation science, depression, pain

Brief summary

Persons with dementia and their caregivers are often cared for in the community through home healthcare (HHC). While these patients and their caregivers need significant help and often have difficulty maintaining their quality of life, home healthcare clinicians are often unprepared to care for this population. This study will therefore examine the ability of an integrated, multi-pronged evidence-based practice intervention for home healthcare registered nurses, occupational therapists and physical therapists, the DSM-H, to improve the quality of care and quality of life for persons with dementia and their family caregiver. The investigators will enroll persons with dementia and their family caregiver upon admission to the HHC agency and examine their quality of life over 60 days following admission, comparing those who receive the intervention to those who serve as controls.

Detailed description

The Dementia Symptom Management at Home (DSM-H) Program is an integrated bundled implementation science intervention to improve interprofessional care in home healthcare (HHC). It consists of training, assessment instruments, patient-caregiver centered care plans and workflow changes. The investigators will perform a cluster randomized controlled clinical trial at a single, urban, non-profit HHC agency, randomizing care teams to either be trained in performing the intervention or serve as controls. The aims of this program are to examine the efficacy of this program to: Aim 1: Measure the effects of DSM-H on pain, neuropsychiatric symptoms, and caregiver rated QOL in the person with dementia receiving HHC. Aim 2: Assess the effects of DSM-H on QOL, burden and depression for the informal caregiver of persons with dementia receiving HHC. Aim 3: Assess the effects of DSM-H on the number of emergency room visits and hospital admissions.

Interventions

BEHAVIORALDementia Symptom Management at Home Program

The DSM-H is a multi-modal interprofessional intervention that includes: 1. intensive training of clinician mentors; 2. disseminated online training for Registered Nurses, Physical Therapists, Occupational Therapists; 3. implementation of evidence-based care plans, assessment instruments, and teaching handouts.

Sponsors

Visiting Nurse Service of New York
CollaboratorOTHER
New York University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patient-caregiver dyad admitted to the HHC agency * Patients must be 65 or older and speak English and/or Spanish. * Patient must have an informal caregiver who is at least 18 years old and spends at least 8 hours per week with the patient. * Patients must score greater than 4 on the cognitive subscale of the Healthy Aging Brain Care Monitor signifying at least mild impairment

Exclusion criteria

* Patients with concomitant axis I disorders other than dementia, depression, adjustment disorders, sleep disorders. * Patients being seen only in the behavioral health unit without another skilled need.

Design outcomes

Primary

MeasureTime frameDescription
Person With Dementia Quality of Life60 DaysQuality of Life in Alzheimer's Disease survey instrument
Caregiver Quality of Life60 DaysCaregiver Targeted Quality of Life survey instrument

Secondary

MeasureTime frameDescription
Caregiver Depression60 daysPublic Health Questionnaire-9 survey instrument
Person with Dementia ER Visits30, 60 daysResource Utilization Inventory survey instrument
Person with Dementia Pain60 daysPain Assessment in Advanced Dementia or Brief Pain Inventory survey instrument
Person with Dementia Functional Status60 daysKatz Activities of Daily Living and Lawton Instrumental Activities of Daily Living assessments
Person with Dementia Hospital Admissions30, 60 daysResource Utilization Inventory survey instrument
Person with Dementia Neuropsychiatric Symptom Burden60 daysHealthy Aging Brain Care Monitor survey instrument

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026