RecruitingNot ApplicableNCT05301543

Insomnia Behavioral Intervention Study

Behavioral Intervention to Reduce Sedative Use in Older Adults With Chronic Insomnia


Sponsor

University of Pennsylvania

Enrollment

20 participants

Start Date

Jan 10, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This randomized pilot study (n=20) explores the effects of a behavioral intervention, that includes sleep hygiene improvements, in long-term users of sleeping pills, aiming to alleviate or stabilize symptoms of insomnia, monitor and decrease sleeping pill usage. Adherence will be monitored by an optional smartphone application.


Eligibility

Min Age: 55 YearsMax Age: 85 Years

Inclusion Criteria6

  • Age of 55-85
  • Use of sleeping pill medication for sleep at least 3 nights a week
  • Diagnosed with Chronic Insomnia by a physician
  • Speaks English above a 6th-grade level
  • Has access to a smartphone and/or smart tablet and can use it
  • Has regular access to internet

Exclusion Criteria2

  • Presence of major depression or other severe psychopathology (e.g., bipolar disorder, psychosis, alcohol/substance abuse, etc.)
  • Presence of an acute or severe medical condition which, in the opinion of the research team, would interfere with the study participant's ability to participate in the research study, such as an acute heart attack, recent severe trauma, etc.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALExperimental: Behavioral approach 1

Includes changing sleep habits and cognitions around sleep from a mental level

BEHAVIORALComparator: Behavioral approach 2

Includes changing sleep habits and awarenes of sleep from a perception level


Locations(1)

University of Pennsylvania School of Medicine

Philadelphia, Pennsylvania, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05301543


Related Trials