Clinical trial Recruiting at 1 site Interventional Ages 25 to 65

Sleep Better, Live Better: a 12-week coaching program to help adults improve sleep and heart-brain health

Official title: A Feasibility Study of the Sleep Better, Live Better Program in a Primary Care-Recruited Population [Sleep Better, Live Better (SBLB) Study]

Run by University of Alabama at Birmingham · NCT07862348 · Data updated 2026-11-12

This trial tests a 12-week, telephone- and text-based sleep coaching program for adults 25–65 with short sleep and higher cardiometabolic risk to see if it improves sleep and related behaviors.

Quick facts

Study typeInterventional
Ages25 Years to 65 Years
SexAll
Enrollment25 (estimated)
SponsorUniversity of Alabama at Birmingham
Academic / other
Locations1 site (Birmingham, Alabama)
StatusRecruiting
StartedOctober 1, 2026
Main results expectedJuly 31, 2027
Study endsJuly 31, 2027
Registry record updatedOctober 7, 2026
Trial IDNCT07862348 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults 25–65 with sleep under 7 hours per night, at least one cardiometabolic risk factor, access to a smartphone, and willingness to engage in a 12-week sleep coaching program.

Probably not a fit

Individuals with very high sleep-disorder scores or barriers to English language participation may gain limited or no benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study enrolls adults aged 25 to 65 with self-reported sleep under 7 hours per night and at least one cardiometabolic risk factor. Participants receive seven structured sleep coaching sessions by phone, plus weekly text check-ins and automated messages over 12 weeks, with engagement and fidelity measured alongside self-reported sleep and sleep-related self-efficacy. The trial will assess feasibility aspects such as recruitment, enrollment, retention, and data collection, as well as preliminary changes in sleep and brain-health related constructs. The program targets a scalable behavioral sleep intervention that could be integrated into primary care for high-risk populations. Results will inform future larger studies and implementation efforts in similar settings.

Why it matters

Potential benefit: If successful, participants may experience improved sleep duration and quality, which could support better cardiometabolic and brain health over time.

How similar studies have gone: Prior behavioral sleep programs have shown feasibility and positive signals in similar populations, though this exact telephone/text-based approach is relatively novel in primary-care settings.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Adults ages 25-65;
2. Self-reported sleep duration \<7 hours per night;
3. Elevated cardiometabolic risk, i.e., presence of one or more of the following - hypertension, obesity, hyperlipidemia, diabetes;
4. Sleep is a behavioral target that individual wants to improve;
5. Complete eligibility screening procedures: Insomnia Severity Index (ISI-7), STOP-BANG, Epworth Sleepiness Scale (ESS);
6. Access to a smartphone, capable of receiving text messages and text links;
7. Able to speak and read English;
8. Willing and able to provide informed consent and participate in all study procedures

Exclusion Criteria:

1. Exceeds eligibility screening thresholds: ISI-7 score ≥22, STOP-BANG score ≥5, ESS score ≥11;
2. Unable to complete study procedures in English;
3. No access to mobile phone with text messaging features;
4. Pregnancy

Where it's running

  • University of Alabama at Birmingham (UAB)
    Birmingham, Alabama, United States
    Recruiting

Study contacts

  • Principal investigator: Ronald M Lazar, PhD — University of Alabama at Birmingham (UAB)
  • Study coordinator: Catherine D Jones, PhD, MSPH
  • Email: catherinejones@uabmc.edu
  • Phone: 205-975-7307

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.