ACTIVE_NOT_RECRUITING

Preventing Insomnia With Virtual Oneshot Therapy (PIVOT)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2022-12-01
Study Completion:2026-12-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05523726

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Individuals with low socioeconomic position as defined by income (\<35k annual household income) or education (high school diploma or less)
  2. * 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.
  1. * Under the age of 18
  2. * Unwilling/unable to participate
  3. * Conditions that could interfere with pCBT-I (including bipolar and seizure disorders)
  4. * Untreated sleep disorders besides insomnia (e.g., sleep apnea, narcolepsy)
  5. * Untreated and severe medical or psychiatric disorders

Contacts and Locations

Principal Investigator

Philip Cheng, Ph.D.
PRINCIPAL_INVESTIGATOR
Henry Ford Health

Study Locations (Sites)

Henry Ford Columbus Medical Center
Novi, Michigan, 48377
United States

Collaborators and Investigators

Sponsor: Henry Ford Health System

  • Philip Cheng, Ph.D., PRINCIPAL_INVESTIGATOR, Henry Ford Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-12-01
Study Completion Date2026-12-01

Study Record Updates

Study Start Date2022-12-01
Study Completion Date2026-12-01

Terms related to this study

Keywords Provided by Researchers

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

Additional Relevant MeSH Terms

  • Insomnia