NCT07444073

Brief Summary

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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
440

participants targeted

Target at P75+ for all trials

Timeline
7mo left

Started Feb 2026

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress40%
Feb 2026Dec 2026

Study Start

First participant enrolled

February 2, 2026

Completed
10 days until next milestone

First Submitted

Initial submission to the registry

February 12, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

March 2, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2026

Last Updated

March 2, 2026

Status Verified

February 1, 2026

Enrollment Period

11 months

First QC Date

February 12, 2026

Last Update Submit

February 25, 2026

Conditions

Keywords

LinAge2Biological AgeGLP-1 Receptor AgonistSemaglutideTirzepatideWeight Management ProgramLifestyleReal-World EvidenceCardiometabolic BiomarkersBody CompositionProspective Cohort

Outcome Measures

Primary Outcomes (1)

  • LinAge2 Biological Age

    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.

    Baseline and 6 months

Secondary Outcomes (30)

  • Change in Body Composition: Body Weight

    Baseline and 6 months

  • Change in Body Composition: Body Mass Index (BMI)

    Baseline and 6 months

  • Change in Body Composition: Waist Circumference

    Baseline and 6 months

  • Change in Body Composition: Hip Circumference

    Baseline and 6 months

  • Change in Body Composition: Waist-to-Hip Ratio

    Baseline and 6 months

  • +25 more secondary outcomes

Study Arms (1)

NOVI Health weight management cohort

Adults newly enrolled in the NOVI Health weight management program receiving standard-of-care GLP-1 receptor agonist therapy (semaglutide or tirzepatide) and lifestyle coaching (diet and physical activity) as part of routine clinical care. Medication type is determined by routine clinical care and patient-clinician decision-making, not by the research study.

Other: Not applicable. This is an observational study.

Interventions

Not applicable. This is an observational study.

NOVI Health weight management cohort

Eligibility Criteria

Age40 Years - 89 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults aged 40-89 years who are overweight or obese and newly enrolled in the NOVI Health weight management program in Singapore. Participants are selected from routine clinical practice at the NOVI Health clinic.

You may qualify if:

  • Adults aged 40-89 years, who are newly enrolled in the NOVI OP+ weight management program.
  • BMI of ≥ 27.5 kg/m2 (if Asian) or 30 kg/m2 (if non-Asian); OR
  • BMI of ≥ 23 kg/m2 (if Asian) / 25 (if non-Asian) kg/m2 in the presence of a weight-related chronic condition (e.g., diabetes, pre-diabetes, polycystic ovarian syndrome, hypertension, fatty liver, high cholesterol).

You may not qualify if:

  • 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.
  • Concomitant anti-diabetic therapy.
  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

NOVI Health (T3 Health PTE LTD)

Singapore, 068914, Singapore

Location

National University of Singapore

Singapore, 119077, Singapore

Location

Related Publications (1)

  • Fong S, Pabis K, Latumalea D, Dugersuren N, Unfried M, Tolwinski N, Kennedy B, Gruber J. Principal component-based clinical aging clocks identify signatures of healthy aging and targets for clinical intervention. Nat Aging. 2024 Aug;4(8):1137-1152. doi: 10.1038/s43587-024-00646-8. Epub 2024 Jun 19.

    PMID: 38898237BACKGROUND

Related Links

MeSH Terms

Conditions

ObesityOverweight

Condition Hierarchy (Ancestors)

OvernutritionNutrition DisordersNutritional and Metabolic DiseasesBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Jan Gruber, PhD

    National University of Singapore

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Zhi Meng Lim, MSc

CONTACT

Hui Ching Michelle Lee, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor

Study Record Dates

First Submitted

February 12, 2026

First Posted

March 2, 2026

Study Start

February 2, 2026

Primary Completion (Estimated)

December 31, 2026

Study Completion (Estimated)

December 31, 2026

Last Updated

March 2, 2026

Record last verified: 2026-02

Locations