Recruiting

CBT-I

Sponsor:

Rutgers, The State University of New Jersey

Code:

NCT06791356

Conditions

Older Adults (65 Years and Older)

Eligibility Criteria

Sex: All

Age: 60+

Healthy Volunteers: Not accepted

Interventions

Cognitive-behavioral therapy for insomnia

Sleep hygiene education

Study Details

Brief summary:

Sleep problems, like insomnia, are common in older African Americans. About 25% of older adults in the US have at least 2 symptoms of insomnia, such as having trouble falling asleep, staying asleep, or getting good sleep for a month or more. Cognitive Behavioral Therapy for Insomnia (CBT-I) is a recommended non-pharmacological treatment for insomnia. Unlike medicines that might only help for a short time or have many side effects, CBT-I deals with the root causes of insomnia. It helps people change how they think and act about sleep, leading to better habits and attitudes. This can make sleep better for a long time, even after the treatment is over. While CBT-I is commonly used among adults with insomnia, its benefits among older adults and specifically older African American adults are not well understood. Thus, the current pilot study will investigate the feasibility of CBT-I in older African American adults and establish preliminary evidence for the potential benefit of CBT-I on sleep as well as cognition in this population.

For this study, participants will be asked to complete pencil-and-paper questionnaires, psychological tests of cognition, 7-day actigraphy, 2 nights of at home sleep monitoring, which collects specific sleep measures such as brain waves and sleep stage timing, and computer-based neuropsychological tests before and after intervention. Study interventions will consist of 8 weekly sleep training sessions via Zoom or a single session of education on strategies to improve sleep quality. Sleep training sessions will include education about strategies to improve sleep quality, changing thought process that contribute to insomnia, training the brain on the optimal sleep environment, and reducing sleep initially to establish a consistent sleep schedule before increasing sleep time. Three months after the post-intervention visit, participants will be asked to come back in for a follow-up evaluation which consists of complete pencil-and-paper questionnaires, psychological tests of cognition, 7-day actigraphy, 2 nights of at home sleep monitoring, and computer-based neuropsychological tests.

Conditions

Older Adults (65 Years and Older)

Study ID

NCT06791356

Start date

Jun 2, 2025

Status verified date

Feb, 2026

Completion date

Jun, 2027

Anticipated

Primary completion date

Jun, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 60+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 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.
  • Subjects must be willing to participate in 8 sessions of CBT-I via Zoom for the CBT-I group.
  • Subjects must be willing to come for pre/post assessment visits.
  • MoCA score of between 20-26.

Exclusion Criteria:

  • Currently taking any of the following medications consistently: Benzodiazepines (ProSom, Restoril, Ativan and Xanax); Z Drugs (eszopiclone (Lunesta), zaleplon (Sonata) and zolpidem (Ambien, Ambien CR, Edluar, and Zolpimist); antidepressants that affect sleep (doxepin, mirtazapine, trazodone); antihistamines (diphenhydramine and doxylamine succinate); barbiturates (methohexital, pentobarbital, primidone, secobarbital).
  • Diagnosed with any sleep disorder other than insomnia (i.e. obstructive sleep apnea using STOP-BANG, restless leg syndrome, REM sleep behavior disorder, etc.).
  • Classified as high fall risk.
  • Primary causes for frequent awakenings are due to a medical condition that is not related to insomnia, such as chronic pain, urinary frequency, upper respiratory infection.
  • Previous experience with CBT-I.

Study Design

Enrollment

20 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: CBT-I

active comparator: Sleep hygiene education

Interventions

Cognitive-behavioral therapy for insomnia

8 sessions of therapy that focus on psychoeducation about sleep hygiene, cognitive restructuring of dysfunctional beliefs that reinforce insomnia, stimulus control to eliminate the association between the bed and wakefulness, sleep restriction in order to establish a consistent sleep schedule, and relaxation training to reduce anxiety that interferes with sleep

Sleep hygiene education

One session of education about behavioral strategies to optimize sleep quality

Primary outcome measure

  • Adherence [ Time Frame: From enrollment to the end of treatment at 8 weeks ]

Central Contacts and Locations

Locations

Rutgers University

Recruiting

Newark, New Jersey, United States, 07102

Contacts

More Information

Sponsor

Rutgers, The State University of New Jersey

Last update posted

Feb 20, 2026

Last verified

Feb, 2026

Keywords

  • insomnia
  • cognitive-behavioral therapy for insomnia
  • African Americans

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Rutgers, The State University of New Jersey on 2026-02-20.