NCT05301543NARecruiting

Insomnia Behavioral Intervention Study

University of Pennsylvania

Start Date

1/10/2022

Completion Date

5/20/2028

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.

Detailed Description

This randomized pilot study has a goal of enrolling 20 study participants. The investigators will examine the effects of a behavioral intervention, that includes sleep hygiene improvements such as regular sleep schedules, with assisted coaching support from the research team. Study participants are long-term users of sleeping pills. The goal is to improve or stabilizie insomnia symptoms and decrease sleeping pill usage. Study participant adherence will be monitored by an optional smartphone application.

Eligibility Criteria

Age Range: 55 years to 85 years

Inclusion Criteria: * 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 Criteria: * 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.

Interventions

BEHAVIORAL

Experimental: Behavioral approach 1

BEHAVIORAL

Comparator: Behavioral approach 2

Interested in This Trial?

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Conditions

Chronic Insomnia

Locations

University of Pennsylvania School of Medicine

Philadelphia, Pennsylvania 19104

United States