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Clinical Trials/NCT06626048
NCT06626048
Active, not recruiting
Not Applicable

Optimizing an Integrated Mind and Body Treatment for Insomnia: The SLEEPS Study

University of California, San Francisco1 site in 1 country10 target enrollmentFebruary 7, 2025

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Insomnia Disorder
Sponsor
University of California, San Francisco
Enrollment
10
Locations
1
Primary Endpoint
Intervention Feasibility
Status
Active, not recruiting
Last Updated
8 months ago

Overview

Brief Summary

This single-arm feasibility trial will provide digital cognitive behavioral therapy for insomnia (CBT-I) and passive body heating (PBH) sessions using a sauna blanket over a 9-week treatment period to adults aged 18 years or older with insomnia disorder.

Detailed Description

Insomnia disorder is a common and consequential mental health problem, with prevalence estimates at approximately 10%. The American College of Physicians recommends cognitive behavioral therapy for insomnia (CBT-I), an efficacious "mind" (psychological and behavioral) treatment, as the first-line treatment for adults with insomnia. Yet, about half of individuals experience residual insomnia symptoms after CBT-I. Accordingly, researchers have sought to augment CBT-I, primarily with pharmacotherapy, but many people do not want to use pharmacologic agents due to concerns about side effects and dependence. Passive-body heating (PBH), a "body" treatment, involves heating the body via hot baths or showers, infrared sauna, or other heat sources. PBH has been found to reduce the time needed to fall asleep and to improve sleep quality. PBH may improve sleep by increasing skin temperature and decreasing core body temperature, a dynamic associated with sleep onset. CBT-I and PBH thus target distinct factors that may contribute to insomnia, and the investigators hypothesize that the combination of CBT-I and PBH holds promise as a multi-component treatment for insomnia disorder.

Registry
clinicaltrials.gov
Start Date
February 7, 2025
End Date
January 28, 2026
Last Updated
8 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years or older
  • English-speaking
  • Willing to use birth control if assigned female sex at birth
  • Location to plug sauna blanket into regular wall outlet
  • Ability to lie in sauna blanket for 15 minutes
  • Ability to fit in the sauna blanket (no taller than 6' 3", no greater than 250 lbs)
  • Daily access to the internet via computer, smartphone, or tablet
  • Elevated insomnia symptoms as indexed by a score of 11 or greater on the Insomnia Severity Index (ISI)
  • Insomnia disorder (characterized by difficulty initiating sleep) as indexed by a positive diagnosis on the Structured Clinical Interview for DSM-5 Sleep Disorders (SCISD)

Exclusion Criteria

  • Night shift worker
  • Current or planned routine body heating practices (e.g., saunas, hot tubs)
  • Pregnant or plans to become pregnant during the participation period
  • Other diagnosed sleep disorders or suspected sleep disorders
  • Medical conditions that might increase the risk of passive body heating using an infrared sauna blanket
  • Mental health disorder that may better explain insomnia, require priority treatment, or be exacerbated by time in bed restriction

Outcomes

Primary Outcomes

Intervention Feasibility

Time Frame: 9 weeks

Proportion of eligible prospective participants who consent to complete at least 6 weeks of at least 3 PBH sessions per week over the 9-week intervention period.

Study Sites (1)

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