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Environmental and Sensory Intervention for Nursing Home Residents With Dementia Who Exhibit Persistent Vocalizations

Study acronym: EASE
StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated February 6, 2025 (before its estimated July 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Study completion date: Aug 2025 to Jul 2025
    • Eligibility criteria shortened, about 6 words
    v3
  2. Start date changed from estimate of Aug 19, 2024 to Oct 31, 2024
    • Eligibility criteria expanded, about 11 words
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Drexel University
28 trials monitored
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Dementia
1,978 trials monitored
See 106 trials at risk
The purpose of this study is to test a person-centered, nature-based non-pharmacological intervention for nursing home residents living with dementia who exhibit persistent vocalizations. The Environmental And Sensory Experience (EASE) involves the projection of a still nature image and the playing of nature sounds. Family members of the person living with dementia provide consent for the resident to participate in the study and complete a brief survey on nature preferences on the resident's behalf. The survey informs the research team on what nature scene to show. Participants will wear a watch that measures stress levels and research staff will monitor vocalization patterns. We will also recruit persons living with dementia from other settings such as assisted living, personal care units, and adult day care settings.
Trial Details
NCT Number NCT06568107
Lead Sponsor Drexel University
Collaborators: National Institute of Nursing Research (NINR)
Conditions
(from sponsor)		 Dementia
Related terms Dementia
Enrollment 32 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov