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Optimizing the Scalability of Evidence-Based Behavioral Sleep Medicine Practices With a Digital Health Platform

N

Noctem

Status

Active, not recruiting

Conditions

Chronic Insomnia
Implementation; Digital Health

Treatments

Other: No Facilitation Support
Other: External and Internal Facilitation Support
Other: External Facilitation Support

Study type

Interventional

Funder types

Industry
Other U.S. Federal agency
Other

Identifiers

NCT04366284
MT190002.01 (Other Grant/Funding Number)
2019-406

Details and patient eligibility

About

The purpose of this study is to compare three different ways to deploy a clinician-decision support platform called NOCTEM COAST among behavioral health care providers who encounter patients with insomnia.

Full description

Insomnia and other sleep disorders are highly prevalent among military service members and compromise readiness, health, and performance; increase the risk of injury; and are associated with astronomical healthcare costs. The first-line treatment recommended for insomnia is cognitive-behavioral treatment for insomnia (CBTI). However, the large number of service members who are in need of this treatment outnumber the clinicians who are experts in behavioral sleep medicine and who currently provide this intervention in a cost-efficient manner and in a way that is acceptable and accessible to patients and clinicians. To address this challenge and scale the delivery and access to evidence-based behavioral sleep interventions, NOCTEM™ has developed a digital health platform called COAST (Clinician Operated Assistive Sleep Technology). However, the most effective way to implement the use of digital sleep health technology, and its comparative impact on patient outcomes, remain to be determined. Therefore, this trial will compare three different ways to deploy the NOCTEM™ platform among behavioral health care providers who encounter patients with insomnia. Specifically, the study will evaluate and compare without external or internal support (NOCTEM), with external support (i.e., facilitation) offered by the NOCTEM team (NOCTEM+EF), and with external support and internal support from local champions (NOCTEM+EF/IF). The trial will also compare the overall magnitude of improvements in insomnia among patients who use the NOCTEM app with their provider.

Enrollment

17 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

For clinicians:

  • Completion of the first half of the workshop or similar Behavioral Sleep Medicine workshop in the past 6 months
  • Completion of the second half of the workshop, including a training session to learn about the use of the NOCTEM platform
  • See patients who present with insomnia
  • Use cognitive-behavioral techniques as part of their practice

For patients:

  • Are service members, veterans, or adult dependents who receive behavioral health care at one of the participating sites
  • Present with complaints of insomnia
  • Own a smart phone or smart device
  • Deemed suitable by their clinician to receive the sleep intervention via the NOCTEM platform
  • Confirm their willingness to use the NOCTEM app for sleep care with their provider

Exclusion criteria

For clinicians:

  • Do not provide direct behavioral health care to service members
  • Do not complete the two-part workshop and the 2-week proficiency training

For patients (recommended):

  • Suspected, diagnosed, or inadequately untreated sleep apnea (less than 4 hours of continuous positive airway pressure [CPAP] use per night)
  • Psychotic symptoms
  • A history of bipolar disorders
  • Women who are pregnant or breastfeeding and parents of children younger than 3 months of age

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

17 participants in 3 patient groups

NOCTEM only (NOCTEM)
Active Comparator group
Description:
No external or internal facilitation
Treatment:
Other: No Facilitation Support
External Facilitation (NOCTEM+EF)
Active Comparator group
Description:
External facilitation only
Treatment:
Other: External Facilitation Support
External and Internal Facilitation (NOCTEM+EF/IF)
Active Comparator group
Description:
External and internal facilitation
Treatment:
Other: External and Internal Facilitation Support

Trial contacts and locations

1

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Central trial contact

Anne Germain, PhD

Data sourced from clinicaltrials.gov

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