Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
ID07135505

The Effect of Early Time-Restricted Eating on Cardiometabolic Health and Circadian Rhythms in Hypertensive Older Adults With Habitual Prolonged Eating Window

Led by University of Alabama at Birmingham · Updated on 2026-02-19

30

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

U

University of Alabama at Birmingham

Lead Sponsor

U

UAB Nutrition Obesity Research Center

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating how early time-restricted eating affects body rhythms and cardiometabolic health in older adults with hypertension. The study focuses on adults aged 60 and older who have a habitual prolonged eating window and elevated blood pressure. The purpose is to understand if limiting eating to an earlier 8-hour window each day can improve health measures related to heart and metabolism. Participants in the study will be randomly assigned to either the early time-restricted eating group or a control group with no intervention. Those in the intervention group will fast for about 16 hours daily and eat freely within an 8-hour window starting between 6:30 and 8:30 am, six days a week for 12 weeks. During fasting, calorie-free drinks, sugar-free gum, and plenty of water are permitted. The study is single-blinded and conducted over a 12-week period. Throughout the study, participants will be monitored for changes in blood glucose, heart rate variability, and systolic blood pressure at the beginning and end of the 12 weeks. They will also be assessed for adherence to the eating schedule and overall health status. The research team will use these measurements to evaluate how early time-restricted eating influences cardiovascular and metabolic health in this population.

CONDITIONS

Brief Title

Early Time-Restricted Eating in Older Adults With Hypertension

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Consent to participate in the study
  • Men and women 60 years old or older
  • Average office systolic blood pressure of 130 mmHg or higher
  • Self-reported eating period of 12 hours or less per day for at least 5 days per week
  • Stable health history over the past 2 months
Not Eligible

You will not qualify if you...

  • Fasting more than 12 hours per day
  • Actively trying to lose weight through a formal program or calorie restriction
  • Weight loss of 10 pounds or more in the last 3 months
  • Unable to wake up regularly between 6 and 8 am
  • Performing overnight shift work more than one day per week on average
  • Resting heart rate over 120 beats per minute
  • Systolic blood pressure over 180 mmHg or diastolic blood pressure over 100 mmHg
  • Diagnosed with diabetes
  • Taking insulin or diabetes medication
  • Unstable angina, heart attack, or stroke in the past 3 months
  • Continuous use of supplemental oxygen for chronic lung or heart failure conditions
  • Pregnant or breastfeeding
  • Rheumatoid arthritis, Parkinson's disease, or currently on dialysis
  • Major psychiatric condition impairing study participation
  • Severe gastrointestinal disease, major gastrointestinal surgery, or active gallstone disease
  • Active cancer treatment in the past year
  • Taking medications that require food intake at least every 12 hours, preventing 16-hour fasting

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 12 weeks

Participants follow an early time-restricted eating schedule, fasting for 16 hours per day with an 8-hour eating window starting between 6:30-8:30 am, 6 days per week.

Weekly visits for 12 weeks

Trial Site Locations

Total: 1 location

1

University of Alabama at Birmingham

Birmingham, Alabama, United States, 35294

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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