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Clinical Trials/NCT05483920
NCT05483920
Completed
Not Applicable

Effects of Sleep Hygiene Education on Sleep Health in Community-Dwelling Older Adults

Black Hills State University1 site in 1 country30 target enrollmentJanuary 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sleep Habit, Good
Sponsor
Black Hills State University
Enrollment
30
Locations
1
Primary Endpoint
Change Score From Baseline to 4-week Follow up on the Sleep Hygiene Index
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

This will be a study looking at trying to change community-dwelling older adults' behavior in regard to good sleep hygiene practices. Investigators will assess the efficacy through subjective outcome measures and objective physiological markers of good sleep through data collected with wearable technology devices.

Detailed Description

Community-dwelling older adults will be recruited and placed into one of two groups. Group one will watch a one-time educational video on sleep hygiene and group two will watch the video plus be sent daily automated text messages to reinforce the education learned in the video. The participants will receive the text messages for a total of 4 weeks. The control group will not receive any intervention during this time frame. Following the initial meeting, all participants will wear the sleep tracker on their wrists during the day and night for 4 weeks. The sleep tracker will monitor the physiological markers of sleep provided by wearable technology on sleep efficiency, time in bed, time actually sleeping, and time spent at each stage of sleep. At the end of the 4-week study period, the researchers will once again meet with each participant. The participant will complete the following questionnaires once again.

Registry
clinicaltrials.gov
Start Date
January 1, 2023
End Date
August 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ashley Pfeiffer

Principal Investigator

Black Hills State University

Eligibility Criteria

Inclusion Criteria

  • Any adult between the ages of 50 and 80 will be recruited for the study

Exclusion Criteria

  • Anyone with a diagnosed sleep disorder such as insomnia or obstructive sleep apnea, and the inability to wear any sleep tracking device on their wrist.

Outcomes

Primary Outcomes

Change Score From Baseline to 4-week Follow up on the Sleep Hygiene Index

Time Frame: Baseline and 4-week follow up

Outcome measure for good sleep hygiene. Scores range from 0-52. Higher scores equate to worse sleep hygiene.

Change Score From Baseline to 4-week Follow up on the Numeric Pain Rating Scale

Time Frame: Baseline and 4-week follow up

Outcome measure for average pain levels. Scores range from 0-10. Higher scores equate to higher pain levels.

Change Score From Baseline to 4-week Follow up on the Pittsburgh Sleep Quality Index

Time Frame: Baseline and 4-week follow up

Outcome measure for quality of sleep. Score ranges 0-21 with higher score equaling poor sleep quality

Change Score From Baseline to 4-week Follow up on the Epworth Sleepiness Scale

Time Frame: Baseline and 4-week follow up

Outcome measure for average daytime sleepiness. Scores range from 0-24. Higher scores equate to worse daytime sleepiness.

Change Score From Baseline to 4-weeks for Participants' Sleep Efficiency Using Wearable Technology.

Time Frame: Baseline, 4-week follow up

Sleep efficiency scores will be calculated using a sleep tracker device and are defined as time spent in bed versus time spent actually sleeping. 85% or higher is considered normal sleep efficiency. The average sleep efficiency score for the first three days at baseline and average sleep efficiency from the last 3 days of the 4 week study period will be used to gather the change score.

Secondary Outcomes

  • Change Scores From Baseline to 4-week Follow up for Participant's Body Mass Index(baseline and 4-week follow up)
  • Change Score From Baseline to 4-week Follow up on the Perceived Stress Scale(Baseline and 4-week follow up)
  • Change Score From Baseline to 4-week Follow up on the Patient Specific Functional Scale(Baseline and 4-week follow up)

Study Sites (1)

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