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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02632318
Other study ID # IRB-36269
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date September 1, 2016
Est. completion date February 1, 2019

Study information

Verified date October 2019
Source VA Palo Alto Health Care System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

One of the most physiologically demanding things that older people do every day is to get up in the morning. After spending a night laying flat, where the blood distributes evenly across the body, when they stand in the morning (and the blood rushes to their feet), their cardiovascular system may not be able to compensate and maintain blood flow to the brain. This phenomenon is known as orthostatic or postural hypotension. The investigators have found in a group of young individuals that use of a dawn-simulation light that gradually wakes the brain is able to increase cardiovascular tone prior to arising. The goal of this experiment is to determine whether this dawn simulation light is able to increase cardiovascular tone in older adults such that they would have reduced or absent postural hypotension when they awaken in the morning. This would greatly reduce the risks of falls and their associated morbidities in older adults.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date February 1, 2019
Est. primary completion date February 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 55 Years to 85 Years
Eligibility Inclusion Criteria:

- History of falls or dizziness at exit from bed in the morning (at least two incidents in the past year)

- At least 20/200 corrected visual acuity

- Stable health

- Normal hearing

Exclusion Criteria:

- Regular cigarette smoker

- Alcohol abuse

- Drug abuse

Study Design


Intervention

Device:
Light
30 minutes of dawn simulation

Locations

Country Name City State
United States VA Palo Alto Health Care System Palo Alto California

Sponsors (3)

Lead Sponsor Collaborator
VA Palo Alto Health Care System Palo Alto Veterans Institute for Research, Velux Fonden

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sympathovagal balance derived from blood pressure measurement measure of sympathovagal balance derived from blood pressure measurement at wake time 30 minutes
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