CClinicalTrials.gg
TerminatedNCT03916588Updated Sep 16, 2021

Dementia Management With Interactive Technology

An observational study in Dementia and Memory Disorders in Old Age, sponsored by Ochsner Health System. Terminated at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2021-09-16.

Sponsored by Ochsner Health System · Observational

Why this study was terminated
covid
Study type
Observational
Model
Ecologic or community
Time perspective
Prospective
Enrollment
89
Ages
18 Years and older
Sex
All
01

Study summary

To investigate the efficacy of an individualized treatment plan delivered through remote technology along with enhanced staff training within a supervised memory unit on patient outcome, care quality, health care utilization/cost, and staff burden. Remote monitoring of activity data will also be explored.

02

Conditions studied

  • Dementia
  • Memory Disorders in Old Age
03

In context

Dementia

2,172 studies on the registry are indexed under Dementia; 540 are open to participants now.

This study's enrollment of 89 is below the median of 250 across 482 observational studies indexed under Dementia.

Browse Dementia studies →

Lead sponsor

Ochsner Health System is the lead sponsor of 54 studies on the registry; 7 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Residents living on the memory care unit will have pre diagnosed advanced dementia or Alzheimer's disease. Subjects will have diminished or no capacity and will require a legally authorized representative.

Eligibility criteria

Inclusion Criteria:

  • Residents living in a specific locked memory care unit in Southeastern Louisiana or
  • Family or staff identified as part of the care team of the resident
05

Study design

Observational model
Ecologic or community
Time perspective
Prospective
Enrollment
89 participants (actual)
Patient registry
No

Groups and cohorts

  • Memory Care Unit Residents

    Residents on a locked memory care unit in southeastern Louisiana will be enrolled. Engaged family members and staff will also consent to provide qualitative information on the resident.

    Behavioral: Individualized Care Plan

Interventions

  • BehavioralIndividualized Care Plan

    Medical, neuropsychological, and social assessment of patient's cognitive, behavioral, medical, and environmental needs with a focus on improving quality of life, reducing health care utilization, and improving staff/family caregiving burden along with a specific plan to address and monitor identified patient and staff/facility needs

06

What researchers measure

Primary outcomes

  1. Mortality/Survival Rate

    Time frame: through study completion, an average of 1 year

  2. Quality of Life Scale (QoL)

    Neuropsychiatric/behavioral symptoms

    Time frame: through study completion, an average of 1 year

  3. Fall Incidence

    Neuropsychiatric/behavioral symptoms

    Time frame: through study completion, an average of 1 year

  4. Zarit Caregiver Burden

    Family burden

    Time frame: through study completion, an average of 1 year

  5. Patient Care Team Burden Scale (PCTB)

    staff caregiver burden

    Time frame: through study completion, an average of 1 year

  6. Healthcare Utilization

    Number of visits to hospital or clinic

    Time frame: through study completion, an average of 1 year

Secondary outcomes

  1. Fitbit Charge HR activity and sleep data

    Average daily steps, minutes asleep

    Time frame: through study completion, an average of 1 year

07

Study locations

1 site
  • Ochsner Health System
    New Orleans, Louisiana 70121, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 16, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03916588
Lead sponsor
Ochsner Health System
Responsible party
Sponsor
First posted
Apr 16, 2019
Start date
Aug 16, 2018
Primary completion
Jul 31, 2020
Completion
Dec 31, 2020
Last update
Sep 16, 2021

Study contacts

R. John Sawyer, PhD
principal investigator · Ochsner Health System

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Sep 2021. You cannot join it, but the record below documents what was studied.

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