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 type | Interventional |
|---|---|
| Ages | 25 Years to 65 Years |
| Sex | All |
| Enrollment | 25 (estimated) |
| Sponsor | University of Alabama at Birmingham Academic / other |
| Locations | 1 site (Birmingham, Alabama) |
| Status | Recruiting |
| Started | October 1, 2026 |
| Main results expected | July 31, 2027 |
| Study ends | July 31, 2027 |
| Registry record updated | October 7, 2026 |
| Trial ID | NCT07862348 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
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Digital storytelling-based psychoeducation to ease loneliness and boost self-efficacy in adults aged 65–74
The study tests whether a digital storytelling–based psychoeducation program can reduce loneliness and improve self-efficacy in adults 65 to 74 who participate in the program versus a comparison group.
-
Online Sleep Education for College Students' Sleep Health and Executive Functioning
A psychoeducational sleep program delivered online will be tested to see if it helps college students improve their sleep health knowledge, sleep quality, and better thinking skills.
-
Helping Men Care for Loved Ones: IN-HOME Outreach for Male Caregivers
This study tests whether outreach from IN-HOME-trained community health workers helps male caregivers improve their knowledge, skills, and confidence, and see if it boosts their health and daily functioning.
-
Health Ahead: Comparing AI vs. Humans for Preventive Health Screening
This study tests AI-assisted screening interpretation against human-only reads to see if automated screening can match or improve current practice for adults, especially in underserved areas.
-
Nurse-led Integrated Home Health Service for Parents of Children Requiring Respiratory Support
This study tests whether a nurse-led home health service helps parents better manage their child’s respiratory symptoms at home.
-
Predicting Birth Type and Breastfeeding Success from Physical Fitness and Emotions in Late Pregnancy
Researchers are testing whether simple grip strength and chair stand tests, plus feelings about childbirth, can help predict delivery type and six-month breastfeeding success for women in their late pregnancy.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.