Actively Recruiting

Phase Not Applicable
Age: 20Years +
All Genders
Healthy Volunteers
NCT06565104

The Sleep2BWell Trial

Led by Columbia University · Updated on 2026-04-14

150

Participants Needed

2

Research Sites

122 weeks

Total Duration

On this page

Sponsors

C

Columbia University

Lead Sponsor

W

Weill Medical College of Cornell University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Improving multiple domains of cardiometabolic health (CMH) through contextual behavioral interventions has the potential to substantially reduce persistent chronic disease disparities. Sleep is critical for preserving CMH and is amenable to intervention in real-world settings. Although sleep health, in conjunction with other lifestyle behaviors, can improve CMH through complementary or synergistic pathways, most existing lifestyle change programs focus solely on diet and physical activity. Sleep2BWell is a community-based cluster randomized trial aimed at evaluating the impact of incorporating a multidimensional sleep health intervention into the BWell4Life program, an ongoing 4-week program for promoting CMH through healthy diet and physical activity, delivered by peer health educators at faith-based organizations and community centers in underserved NYC neighborhoods. The enhanced 6-week intervention, Sleep2BWell, will include the following additional components: 1) two sleep health education and group coaching sessions, 2) self-monitoring and motivational enhancement using a Fitbit, and 3) addressing prevalent environmental barriers to healthy sleep in urban settings such as noise and light with a novel and timely extension to address indoor air pollution. A total of 10 community sites will receive the intervention enrolling an average of 15 participants per site for an expected sample of 150. The investigators will collect objective measures of sleep and physical activity throughout the study, and assess diet and CMH outcomes at baseline and 10 weeks (primary endpoint). The investigators hypothesize that Sleep2BWell will improve CMH, including reduced blood pressure (primary outcome) improved health behaviors (sleep, diet, physical activity) and adiposity markers (secondary outcomes). To ensure the successful completion and future expansion of this work, this study will use mixed methods to understand implementation determinants and outcomes, guided by implementation science frameworks. This first-of-its-kind effectiveness-implementation study, addressing individual level behaviors and factors and upstream influences and leveraging key behavior change and community engagement strategies, will investigate the integration of sleep health into a multi-behavior lifestyle change intervention aimed at addressing CMH disparities in community settings. This innovative multilevel intervention will inform scalable sustainable community health approaches and public health policy to improve sleep health and CMH disparities through advancement in novel multilevel bundled behavioral interventions.

CONDITIONS

Official Title

The Sleep2BWell Trial

Who Can Participate

Age: 20Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • English- and/or Spanish-speaking
  • Aged 20 years or older
  • Having systolic blood pressure in the elevated or hypertension category (120 mmHg or higher)
Not Eligible

You will not qualify if you...

  • Known medical conditions preventing safe participation, such as neurological degenerative diseases (e.g., Parkinson's), severe psychiatric disorders, or substance use disorder
  • History of cardiovascular disease or cancer
  • Pregnant or planning to become pregnant during the study
  • Less than one year postpartum

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Weill Cornell Medicine

New York, New York, United States, 10021

Actively Recruiting

2

Columbia University Irving Medical Center, Mailman School of Public Health

New York, New York, United States, 10032

Actively Recruiting

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Research Team

R

Research Project Coordinator

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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