Aging Well: Targeting Obesity With GLP-1 Agonists to Enhance Physical and Vascular Health in Postmenopausal Women

NCT07057310 | Enrolling By Invitation Phase 4 FDA Drug

• 1 other identifier: 24-010834
• Study Type: interventional
• Target: 30
• Locations: 1 country
• Sites: 1

Brief Summary

In postmenopausal women, obesity increases the risk of physical function decline, premature aging, and vascular dysfunction. Semaglutide and tirzepatide are potent obesity medications. The goal is to determine the effect of weight loss induced by the new generation of GLP-1 receptor agonists on physical function, aging biomarkers, and vascular function in postmenopausal women with obesity.

Conditions

Obesity; Menopause

Keywords

obesity; vascular function; aging; postmenopause; women

Outcome Measures

Primary Outcomes (11)

• Physical Function Measure: Short Physical Performance Battery (SPPB) score.

  The SPPB is a standardized test that evaluates lower extremity function using three components: balance tests (standing in various positions), gait speed (walking a short distance), and chair stand (repeated standing from a seated position). Each component is scored from 0 to 4; the total score ranges from 0 to 12. Higher scores represent better physical function.

  24 weeks

• Physical Function Measure: Modified Clinical Test of Sensory Interaction in Balance (mCTSIB) performed on the Rehabilitation Artificial Physical Intelligence Database (RAPID) foot pressure mat

  The mCTSIB assesses balance under four sensory conditions: eyes open/closed on firm and foam surfaces. Testing is performed while standing on the RAPID foot pressure mat, which captures center of pressure and postural sway data. The primary measure is average sway area of the four sensory conditions. The sway area is the area which is required to correct equilibrium, representing the total area covered by postural sway, measured in square centimeters (cm²).

  24 weeks

• Physical Function Measure: Standing Chest Throw Test with a 2-kg Weighted Ball using Motion Sensor Technology (MST)

  This test evaluates upper body muscular power. Participants perform a two-handed chest throw of a 2-kg medicine ball from a standing position. The MST is used to record throw distance, velocity, and related performance metrics. The primary measure is Peak Power Score (W).

  24 weeks

• Physical Function Measure: Chair-to-Stand Tests using Motion Sensor Technology (MST)

  This test assesses lower body strength and function. Participants are instructed to stand up from a chair and sit back down five times without using their arms. The MST measures movement dynamics. The primary measure is peak power score (W).

  24 weeks

• Physical Function Measure: Six-Minute Walk Test (6MWT)

  The 6MWT is a standardized submaximal exercise test used to assess functional aerobic capacity. Participants are instructed to walk as far as possible in six minutes along a flat, straight course. The total distance walked is recorded in feet. Longer walking distances indicate better aerobic capacity and endurance.

  24 weeks

• Physical Function Measure: Hand Grip Strength using a Hydraulic Hand Dynamometer

  Participants are instructed to squeeze the dynamometer with maximum effort, measured in kilograms. The highest value from multiple trials is recorded.

  24 weeks

• Physical Function Measure: Short Form-12 (SF-12) Health Survey

  The SF-12 is a standardized, self-administered questionnaire designed to assess overall health-related quality of life. It includes 12 items that measure physical and mental health components, generating Physical Component Summary (PCS) and Mental Component Summary (MCS) scores. Scores are standardized on a scale where higher values indicate better health status. Both PCS and MCS scores typically range from 0 to 100, with 0 indicating the poorest health and 100 indicating the best possible health status.

  24 weeks

• Physical Function Measure: Patient-Reported Outcomes Measurement Information System (PROMIS) - Fatigue and Physical Function Domains

  The PROMIS is a standardized set of self-reported questionnaires designed to measure health domains. This study includes the fatigue and physical function domains, which assess the participant's perceived level of tiredness and ability to perform daily physical activities. Responses generate standardized T-scores, calibrated to the general population. Higher fatigue T-scores indicate greater fatigue severity.

  24 weeks

• Aging Biomarkers: Cellular Senescence Markers in Plasma

  Cellular senescence markers are measured in plasma samples to assess biological aging and cellular stress. These markers may include proteins associated with the senescence-associated secretory phenotype (SASP). Quantification is performed using immunoassays. Higher levels of senescence markers indicate increased cellular senescence.

  24 weeks

• Difference between biological and chronological age

  Epigenetic clocks estimate biological age by analyzing DNA methylation patterns at specific CpG sites across the genome. Biological age estimates are compared to chronological age to assess aging acceleration or deceleration. Biological age greater than chronological age indicates accelerated biological aging and potential increased risk of morbidity and mortality. Primary measure is the difference (ΔAge) between biological and chronological ages = reported in years.

  24 weeks

• Vascular Function Assessment: Reactive Hyperemia Index (RHI) using EndoPAT

  The RHI is measured using the EndoPAT device, which assesses endothelial function by evaluating changes in digital pulse volume during reactive hyperemia. This non-invasive test involves occluding blood flow in one arm followed by release to induce vasodilation, with pulse amplitude recorded via finger probes. Lower RHI values suggest endothelial dysfunction and increased cardiovascular risk.

  24 weeks

Study Arms (2)

Weight loss medication and standard lifestyle intervention

EXPERIMENTAL

Subjects will receive tirzepatide or semaglutide in combination with a standard lifestyle intervention.

Drug: semaglutide or tirzepatide; Behavioral: Lifestyle modification intervention

Standard lifestyle intervention only

ACTIVE COMPARATOR

Subjects will receive standard of care lifestyle intervention only.

Behavioral: Lifestyle modification intervention

Interventions

semaglutide or tirzepatide DRUG

Semaglutide and tirzepatide will be dosed as per prescription labels

Weight loss medication and standard lifestyle intervention

Lifestyle modification intervention BEHAVIORAL

All participants will be recommended the following: 1) low-calorie diet based on their predicted by Harris Benedict resting energy expenditure minus 500 kcal per day; 2) physical activity: a goal of 10,000 steps or more per day; 3) exercise: a goal of 150 minutes or more of moderate-intensity aerobic activity (cardiovascular exercise) per week; 4) limited consumption of liquid calories (i.e. sodas, juices, alcohol, etc.).

Standard lifestyle intervention only; Weight loss medication and standard lifestyle intervention

Eligibility Criteria

• Age: 46 Years - 60 Years
• Gender Eligibility Details: Cis-Gender
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Postmenopausal women (with menopause defined as the cessation of menstrual periods for at least 12 months or history of bilateral oophorecomy)
• Age 46-60 years old
• BMI ≥ 30 kg/m2.

You may not qualify if:

• Past or current use of menopausal hormone therapy
• Early or premature menopause
• History of chemically induced menopause
• Impaired renal function (GFR ≤29)
• Thyroid-stimulating hormone ≥7 with low free T4
• Diabetes
• Cardiovascular disease
• Elevated blood pressure (\>170/\>95)
• Uncontrolled co-morbidities including inflammatory, autoimmune, infectious, hepatic, gastrointestinal, malignant, or psychiatric disease
• \>5% change in weight during the 3 months prior to screening
• Other anti-obesity medication use within the past 3 months
• History of bariatric surgery
• History of malignant neoplasms within the past 5 years prior to screening
• Current use of supplements known to affect weight
• Personal or family history of medullary thyroid cancer.

Sponsors & Collaborators

• Mayo Clinic: lead

Study Sites (1)

Mayo Clinic in Florida

Jacksonville, Florida, 32224, United States

Location

Related Links

• Mayo Clinic Clinical Trials

MeSH Terms

Conditions

Obesity

Interventions

semaglutide; Tirzepatide

Condition Hierarchy (Ancestors)

Overweight; Overnutrition; Nutrition Disorders; Nutritional and Metabolic Diseases; Body Weight; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Glucagon-Like Peptide-1 Receptor; Glucagon-Like Peptide Receptors; Receptors, G-Protein-Coupled; Receptors, Cell Surface; Membrane Proteins; Proteins; Amino Acids, Peptides, and Proteins; Receptors, Gastrointestinal Hormone; Receptors, Peptide

Study Officials

• Maria D. Hurtado Andrade, M.D., Ph.D.

  Mayo Clinic

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 4
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Model Details: This will be a 24-week, open-label, pragmatic, randomized clinical trial. Participants will be randomized 1:1 to receive tirzepatide or semaglutide with a standard lifestyle intervention or a lifestyle intervention alone. Tirzepatide or semaglutide will be started at the lowest dose and titrated every four weeks, as tolerated, up to the maximum dose of 2.4 mg weekly for semaglutide and 15 mg weekly for tirzepatide. The choice of the medication will depend on patient's preference, cost, and drug availability. We will assess body composition, measurements of physical function, obtain a blood sample for the measurement of aging biomarkers, and perform vascular testing at different timepoints.

Study Record Dates

• First Submitted: May 5, 2025
• First Posted: July 9, 2025
• Study Start: May 1, 2025
• Primary Completion (Estimated): December 31, 2026
• Study Completion (Estimated): March 31, 2027
• Last Updated: July 9, 2025

Record last verified: 2025-06

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)