Skip to content

Preventing Insomnia With Virtual Oneshot Therapy (PIVOT)

Preventing Insomnia and Depression With Nurse Coaching in Individuals With Low Socioeconomic Position

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05523726
Enrollment
167
Registered
2022-08-31
Start date
2022-12-01
Completion date
2026-03-13
Last updated
2026-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insomnia

Keywords

Insomnia, Depression, Digital Nurse Coaching, CBT-I, preventative therapy

Brief summary

This study is intended to assess the efficacy of preventative Cognitive Behavioral Therapy for Insomnia (pCBT-I) on reducing the severity and stopping the progression of acute insomnia and depression. We also hope to gain a deeper understanding of the sociocultural, interpersonal, and individual factors that may have a role in development of insomnia and/or engagement with treatment plans.

Detailed description

Insomnia is a debilitating condition that escalates the risk of a myriad of disorders and is a source of significant economic burden. Insomnia takes an immense toll on individuals' physical and mental wellbeing and treating it before it can develop into chronic insomnia can save individuals untold time and money on treatment. This study is intended to assess the effects of one virtual pCBT-I session with a nurse coach on reducing the severity and stopping the progression of acute insomnia and depression. The benefits of pCBT-I have been demonstrated in prior studies but have yet to be tested on larger sample populations. Participants will be recruited from the Henry Ford Health System (HFHS) outpatient network, as well as the Medicare/Medicaid data warehouse and other community partners. Subjects will be screened to determine eligibility, and then will be randomized into one of two insomnia treatment groups (control digital sleep education and pCBT-I via telehealth coaching). Upon completion, the proposed research will not only have validated a preventative treatment for both insomnia and depression, but we will have the tools to apply it in the most effective way possible.

Interventions

BEHAVIORALpCBT-I

Telehealth coaching

Sponsors

Henry Ford Health System
Lead SponsorOTHER
University of Michigan
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Masking description

The principle investigator will be blind to the group assignment

Intervention model description

Random assignment into experimental and control conditions at a 1:1 ratio

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Individuals with low socioeconomic position as defined by income (\<35k annual household income) or education (high school diploma or less) * Experiencing symptoms of prodromal acute insomnia (difficulty falling asleep, difficulty staying asleep, or problems waking up too early), along with worry or distress regarding their symptoms.

Exclusion criteria

* Under the age of 18 * Unwilling/unable to participate * Conditions that could interfere with pCBT-I (including bipolar and seizure disorders) * Untreated sleep disorders besides insomnia (e.g., sleep apnea, narcolepsy) * Untreated and severe medical or psychiatric disorders

Design outcomes

Primary

MeasureTime frameDescription
Insomnia Severityup to one year post-treatmentInsomnia Severity Index Score (0 to 28; higher scores correspond to worse severity)
Depression Severityup to one year post-treatmentQIDS-SR16 Score (0-27; higher scores correspond to worse severity)
Cases of DSM-5 Insomnia6 months post-treatmentMeet all DSM-5 criteria for Chronic Insomnia
Cases of Clinically Significant Depression6-months post-treatmentQIDS-SR16 score of 11 or higher

Secondary

MeasureTime frameDescription
Physical EnvironmentThrough study completion, an average of 1 yearParticipants will be asked about the layout of their sleep environment as well as neighborhood characteristics. Sleep environment will be assessed using qualitative information on individual's surroundings and information such as their ability to adjust light levels, temperature, and sound. If it is easier for the individual to adjust these, then they have a better physical environment for sleep. Neighborhood characteristics will be evaluated with the Neighborhood Safety scale (scores range from 1 to 5; lower scores indicate more neighborhood safety).
Sociocultural EnvironmentThrough study completion, an average of 1 yearSociocultural environment is measured using a household roster and the Everyday Discrimination Scale. A household roster will ask participants to report the number of individuals in the household and characterize the relationship with the participant. No summary score exists for the household roster. The Everyday Discrimination Scale measures frequency of discrimination (scores range from 10 to 60; higher scores represent more frequent experiences of discrimination).

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORPhilip Cheng, Ph.D.

Henry Ford Health

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026