Current partner codePEPTIDESDE
NCT07444073·Not applicable·OBSERVATIONAL

Assessing Biological Aging in a Real-World Medical Weight Loss Program Using the LinAge2 Clinical Clock

Status

Not yet recruiting

Phase

Not applicable

Enrollment

440

Locations

2

Results

Not posted

Publications

1

Study summary

What the protocol is testing.

This study examines whether routine treatment with semaglutide or tirzepatide, prescribed with lifestyle coaching in a real-world weight-management program, is associated with changes in biological age measured by the LinAge2 clinical aging clock over 6 months.

Full detailed description

This study will evaluate whether routine treatment with semaglutide or tirzepatide, prescribed in conjunction with lifestyle coaching support as part of standard-of-care in a real-world clinical weight-loss program, is associated with changes in biological age as measured by the LinAge2 clock. Aging is a primary driver of chronic disease, functional decline, and mortality. Obesity, through mechanisms such as mitochondrial dysfunction, oxidative stress, and chronic inflammation, may accelerate biological aging. Given that GLP-1 receptor agonists such as semaglutide and tirzepatide improve metabolic and cardiovascular health, this study will examine whether these benefits extend to biological aging as quantified by LinAge2, a clinical aging clock derived from standard clinical biomarkers. This is a six-month prospective observational cohort study involving approximately 440 adults aged 40-89 years who are overweight or obese and newly enrolled in the weight management program at NOVI Health (T3 Health PTE LTD), a private healthcare provider in Singapore. Clinical care and program delivery are provided by NOVI Health as part of routine practice. Participants will receive standard-of-care GLP-1 RA therapy (semaglutide or tirzepatide) together with personalized diet and physical activity interventions. Study procedures include baseline and six-month visits at the NOVI Health clinic, where anthropometry, body composition, blood and urine samples, questionnaires, and functional performance assessments will be conducted. Blood and urine samples will be collected by trained and certified nurses or phlebotomists, analyzed by an accredited external laboratory, and discarded thereafter; no biological materials will be stored. The National University of Singapore (NUS) research team provides scientific leadership in study design and conducts the development and application of the LinAge2 biological aging clock and analyses of de-identified data generated during routine clinical care at NOVI Health. NUS is not involved in participant recruitment, informed consent, clinical procedures, drug prescription, or biospecimen handling. The primary outcome is change in LinAge2 biological age from baseline to six months. Secondary outcomes include changes in body composition, cardiometabolic biomarkers, and functional clinical measures.

Interventions

Treatment arms and agents.

OTHER

Not applicable. This is an observational study.

Not applicable. This is an observational study.

Timeline

From registration to results.

  1. First posted

    Mar 2, 2026

  2. Study start

    Jun 1, 2026

  3. Primary completion

    Dec 31, 2026

  4. Study completion

    Dec 31, 2027

  5. Results posted

    Not reported

  6. Registry updated

    Jul 1, 2026

Outcomes

What the study measures.

Primary outcomes

LinAge2 Biological Age

Time frame · Baseline and 6 months

The primary outcome of this study is to determine the change in LinAge2 biological age estimates in response to the NOVI Health weight management program, which comprises GLP-1 RA therapy alongside personalized diet and physical activity interventions.

Secondary outcomes

Change in Body Composition: Body Weight

Time frame · Baseline and 6 months

Body weight measured in kilograms (kg); outcome is change from baseline to 6 months.

Change in Body Composition: Body Mass Index (BMI)

Time frame · Baseline and 6 months

BMI calculated as weight (kg) divided by height (m²), reported in kg/m².

Change in Body Composition: Waist Circumference

Time frame · Baseline and 6 months

Waist circumference measured in centimeters (cm) using a measuring tape

Change in Body Composition: Hip Circumference

Time frame · Baseline and 6 months

Waist circumference measured in centimeters (cm) using a measuring tape

Change in Body Composition: Waist-to-Hip Ratio

Time frame · Baseline and 6 months

Waist-to-hip ratio calculated as waist circumference / hip circumference

Change in Pulse Rate

Time frame · Baseline and 6 months

Pulse rate measured in beats per minute (bpm)

Change in Blood Pressure

Time frame · Baseline and 6 months

Systolic and Diastolic blood pressure measured in mmHg

Change in Body Composition: Body Fat Percentage

Time frame · Baseline and 6 months

Body fat percentage (%) measured using a Tanita body composition analyzer (bioimpedance)

Change in Body Composition: Muscle Mass

Time frame · Baseline and 6 months

Muscle mass measured in kilograms (kg) using a Tanita body composition analyzer (bioimpedance)

Change in Body Composition: Basal Metabolic Rate

Time frame · Baseline and 6 months

Basal metabolic rate measured in kilocalories per day (kcal/day) as estimated by a Tanita body composition analyzer (bioimpedance)

Eligibility

Who can take part.

Minimum age
40 Years
Maximum age
89 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria * Adults aged 40-89 years, who are newly enrolled in the NOVI OP+ weight management program. * BMI of ≥ 30 kg/m2 (obesity); OR * BMI of ≥ 27 kg/m2 to \< 30 kg/m2 (overweight) in the presence of at least one weight-related comorbid condition e.g. dysglycemia (prediabetes or type 2 diabetes mellitus), hypertension, dyslipidemia, obstructive sleep apnea or cardiovascular disease. Exclusion Criteria * Pregnancy or lactation. * Non-ambulatory status, total blindness, complete hearing loss, or inability to speak. * Medical history of, or self-reported, psychiatric illness, congenital or irreversible neurodegenerative diseases, cognitive impairment, or eating disorders that may affect adherence or assessment outcomes. * On GLP-1 RA, sulfonylurea or insulin medications for the past 3 months. * Active cancer on chemotherapy or immunotherapy. * Known hypersensitivity or contraindications to GLP-1 RAs. * Any condition, in the opinion of the attending clinician, that would jeopardize participant safety or interfere with study compliance.

Study locations

2 registered sites.

Singapore. Showing up to 24 locations stored in the fast local snapshot.

NOVI Health (T3 Health PTE LTD)

Singapore, Singapore

National University of Singapore

Singapore, Singapore

Related trials

More studies on Tirzepatide.

Related PeptideStat pages

Put the record in context.

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