Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
ID06791356

Cognitive Behavioral Therapy for Insomnia in Older African American Adults

Led by Rutgers, The State University of New Jersey · Updated on 2026-02-20

20

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

R

Rutgers, The State University of New Jersey

Lead Sponsor

N

National Institute on Aging (NIA)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Sleep difficulties like insomnia are common among older African American adults, with about a quarter of older adults in the US experiencing symptoms such as trouble falling or staying asleep for a month or longer. Cognitive Behavioral Therapy for Insomnia (CBT-I) is a non-drug treatment that addresses the underlying causes of insomnia by changing thoughts and behaviors about sleep. This approach may improve sleep quality for a long time, but its effects specifically in older African American adults have not been well studied. This pilot study aims to evaluate the feasibility of CBT-I in this group and gather early evidence of its potential benefits on sleep and cognitive function. Participants will either receive eight weekly CBT-I sessions via Zoom, focusing on sleep education, changing sleep-related thinking, training the brain for optimal sleep environments, and setting a consistent sleep schedule by initially limiting sleep time before increasing it. Another group will have one session providing education about improving sleep quality. The study includes pre- and post-intervention assessments along with a three-month follow-up. Throughout the study, participants will complete paper questionnaires, cognitive tests, 7-day wrist activity monitoring (actigraphy), and two nights of at-home sleep monitoring that measures brain waves and sleep stages. Computer-based neuropsychological tests will also be done before and after treatment, and again at follow-up three months later. Researchers will measure adherence to treatment over eight weeks, sleep efficiency, and cognitive performance to understand the effects of the interventions.

CONDITIONS

Brief Title

CBT-I in Older African American Adults

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Reading level 6th grade or better and can speak and understand English well
  • Self-identify as African American or Black
  • Ages 60 and over
  • Score of >2 in PSQI sleep duration, sleep disturbance, or overall sleep quality calculated components
  • Participating in the "Pathways to Healthy Aging in African Americans" study
  • Has established chronic insomnia issues for at least three months
  • Willing to participate in 8 sessions of CBT-I via Zoom for the CBT-I group
  • Willing to come for pre/post assessment visits
  • MoCA score of between 20-26
Not Eligible

You will not qualify if you...

  • Currently taking benzodiazepines, Z drugs, antidepressants affecting sleep, antihistamines, or barbiturates consistently
  • Diagnosed with any sleep disorder other than insomnia (e.g., obstructive sleep apnea, restless leg syndrome, REM sleep behavior disorder)
  • Classified as high fall risk
  • Frequent awakenings primarily caused by a medical condition unrelated to insomnia such as chronic pain, urinary frequency, or upper respiratory infection
  • Previous experience with CBT-I

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Outpatient Treatment

Duration - 8 weeks

Participants receive 8 sessions of cognitive-behavioral therapy for insomnia or one session of sleep hygiene education.

8 therapy sessions via Zoom and pre/post assessment visits

Trial Site Locations

Total: 1 location

1

Rutgers University

Newark, New Jersey, United States, 07102

Actively Recruiting

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Research Team

P

Payton White

B

Bernadette A Fausto, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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