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Smart ambient bright light for Caregiver

N/A
Recruiting
Led By Ying-Ling Jao, PhD
Research Sponsored by Penn State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Age≥55
Nursing home residency≥3 months
Timeline
Screening 3 weeks
Treatment Varies
Follow Up weeks 1, 3, 5, 7, 9, 11, and 13
Awards & highlights

Study Summary

This trial will test a system that combines natural daylight with LED lights to reduce agitation in people with Alzheimer's Disease & Related Dementias in nursing homes. It will also measure the system's effectiveness, feasibility & fidelity.

Who is the study for?
This trial is for nursing home residents aged 55 or older who have been living in the home for at least three months, speak English, and have a clinical diagnosis of Alzheimer's Disease or related dementia with recent agitation.Check my eligibility
What is being tested?
The study tests a smart ambient bright light (SABL) system designed to mimic natural daylight cycles. It aims to reduce agitation in people with dementia by automatically adjusting indoor lighting based on time and available natural light over four weeks.See study design
What are the potential side effects?
Since this intervention involves environmental lighting adjustments rather than medication, traditional side effects are not expected. However, changes in light may affect sleep patterns or mood.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am 55 years old or older.
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I have been living in a nursing home for at least 3 months.
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I have been diagnosed with Alzheimer's Disease or a similar type of dementia.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~weeks 1, 3, 5, 7, 9, 11, and 13
This trial's timeline: 3 weeks for screening, Varies for treatment, and weeks 1, 3, 5, 7, 9, 11, and 13 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in agitation
Change in light level: CS at the facility level
Change in light level: CS at the individual level
+5 more
Secondary outcome measures
Adverse effects.
Affect
Behavioral and Psychological Symptoms of Dementia (BPSD)

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Smart ambient bright lightExperimental Treatment1 Intervention
The smart ambient bright light (SABL) intervention provides auto-controlled, consistent indoor lighting that incorporates natural daylight.
Group II: ControlPlacebo Group1 Intervention
Usual light.

Find a Location

Who is running the clinical trial?

Penn State UniversityLead Sponsor
355 Previous Clinical Trials
125,717 Total Patients Enrolled
Ying-Ling Jao, PhDPrincipal InvestigatorPenn State University

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the upper limit of enrollees in this experiment?

"Affirmative. Clinicaltrials.gov clearly displays this clinical trial as actively recruiting, which was initially posted on April 24th 2023 and most recently edited on December 12th 2023. The study is admitting 40 patients across two sites."

Answered by AI

Does this trial currently need more participants?

"Affirmative. Data posted on clinicaltrials.gov confirms that this experiment, initially published April 24th 2023, is actively enrolling participants. 40 individuals must be gathered from two different medical facilities."

Answered by AI
~20 spots leftby Apr 2025