Recruiting NA Older Adults (65 Years and Older)

New treatment option for Older Adults (65 Years and Older)

Official title CBT-I in Older African American Adults

ClinicalTrials.gov ID: NCT06791356

What this study is testing

What it's testing
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.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 60 and older

You may be able to join if

  • 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.

You likely can't join if

  • Currently taking any of the following medications consistently: Benzodiazepines (ProSom, Restoril, Ativan and Xanax); Z Drugs (eszopiclone (Lunesta)...
  • Diagnosed with any sleep disorder other than insomnia (i.e. obstructive sleep apnea using STOP-BANG, restless leg syndrome, REM sleep behavior...
  • 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...
  • Previous experience with CBT-I.
See the full eligibility criteria
Who can join
  • 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.
  • people must be willing to participate in 8 sessions of CBT-I via Zoom for the CBT-I group.
  • people must be willing to come for pre/post assessment visits.
  • MoCA score of between 20-26.
What rules you out
  • 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...
  • 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.

The study team makes the final eligibility decision.

Where it's taking place

  • Newark, New Jersey, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 60 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Newark, New Jersey, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.