Clinical trial Recruiting at 1 site Interventional Ages 50 and up

Nature-based intervention for nursing home residents with dementia

Official title: A Person-Centered Environmental and Sensory Intervention for Nursing Home Residents With Dementia Who Exhibit Persistent Vocalizations

Run by Drexel University · NCT06568107 · Data updated 2026-11-12

This study is testing a nature-based program to see if it can help nursing home residents with dementia reduce their vocalizations and feel less stressed.

Quick facts

Study typeInterventional
Ages50 Years and up
SexAll
Enrollment32 (estimated)
SponsorDrexel University
Academic / other
Locations1 site (Philadelphia, Pennsylvania)
StatusRecruiting
StartedOctober 31, 2024
Main results expectedJuly 2025
Study endsJuly 2025
Registry record updatedFebruary 6, 2025
Trial IDNCT06568107 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are nursing home residents aged 50 and older with severe dementia and a history of persistent vocalizations.

Probably not a fit

Patients who are blind, deaf, or show dissent will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study tests a person-centered, nature-based intervention called the Environmental And Sensory Experience (EASE) for nursing home residents with dementia who exhibit persistent vocalizations. Participants will engage in three visits where their vocalization behaviors will be observed, and they will wear a watch to monitor stress levels. Family members will provide consent and complete a survey to inform the nature scenes used during the intervention. The study aims to assess the feasibility and efficacy of EASE in reducing vocalizations and evaluate staff perceptions of its acceptability.

Why it matters

Potential benefit: If successful, this intervention could significantly reduce distressing vocalizations in dementia patients, improving their quality of life.

How similar studies have gone: While this approach is innovative, similar non-pharmacological interventions have shown promise in improving outcomes for dementia patients.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* The participants must: 1) have a medical diagnosis of dementia; 2) have severe dementia as determined by a MMSE score of ≤9 (or another cognitive test indicating severe dementia); 3) have a history of PVs per staff report; 4) be 50 years older or greater; 5) require extensive assistance by staff to ambulate or is non-ambulatory (to allow for consistent video recording). In addition, consent will be obtained from the resident's Legally Authorized Representative (LAR) and assent from the participant.

Exclusion Criteria:

* Persons living with dementia will be excluded if they: 1) are blind; 2) are deaf; 3) give indications of dissent. Variations will be sought for gender, race and ethnicity.

Where it's running

  • Drexel University
    Philadelphia, Pennsylvania, United States
    Recruiting

Study contacts

  • Principal investigator: Justine S Sefcik — Drexel University
  • Study coordinator: Justine S Sefcik, PhD, RN
  • Email: jss398@drexel.edu
  • Phone: 6074347205

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.