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RecruitingNCT07456449Updated May 5, 2026

Collagen Peptides and Cellular Aging

An interventional study of Collagen peptides and Maltodextrin (Placebo) in Longevity, Healthy Aging and Biological Ageing, sponsored by University of Vienna. Recruiting at 1 site in Austria. Open to participants aged 50 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-05.

Sponsored by University of Vienna · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
125
Allocation
Randomized
Ages
50 Years to 70 Years
Sex
All
01

Study summary

The goal of this clinical trial is to learn if daily collagen peptide supplementation can stabilize or lengthen telomeres and improve related markers of cellular aging in adults aged 50-70 years with overweight and low-to-moderate physical activity (healthy volunteers without major chronic disease).

Main questions it aims to answer are:

Does six months of collagen peptides stabilize or extend telomere length and increase telomerase activity compared with placebo? Are any telomere-related changes associated with lower inflammation, healthier body composition, and better functional health?

Researchers will compare collagen as an intervention to a placebo group to see if collagen will influence aging markers.

Participants will take collagen peptides or a placebo daily for 24 weeks. They will attend three study visits: one before starting the intervention (T0), one at 3 months (T1), and one at 6 months (T2). At each visit, blood samples will be collected to measure telomere length, telomerase activity, and inflammation/redox markers. Participants will also undergo body composition assessments using bioelectrical impedance, complete functional tests of muscle strength and mobility, and fill out questionnaires on health and vitality.

02

Conditions studied

  • Longevity
  • Healthy Aging
  • Biological Ageing

Keywords

  • Aging
  • Collagen
  • Supplements
  • Patient Care
  • Healthspan
  • Cellular aging
03

Who can participate

Ages eligible
50 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Adults aged 50-70 years; both male and female participants are eligible
  • Body mass index (BMI) 25-30 kg/m²
  • Low to moderate physical activity: not meeting current WHO recommendations (\<150 minutes/week) or ≤2 sessions/week structured training
  • Able to live independently and mobile in daily life
  • No regular resistance training within the past 6 months
  • Provision of written informed consent

Exclusion criteria

Exclusion Criteria:

  • Diagnosed chronic diseases relevant to the immune system, metabolism, or cellular aging (e.g., diabetes mellitus, cancer, cardiovascular, rheumatologic diseases)
  • Use of immunomodulatory, systemic anti-inflammatory, or hormonal medications (e.g., corticosteroids, immunosuppressants)
  • Acute infections or surgeries within the last 3 months
  • Regular use of supplements known to affect oxidative stress or cellular aging (e.g., high-dose antioxidants, CoQ10, omega-3 fatty acids, high-dose vitamin D)
  • Participation in another clinical study within the last 3 months
  • Vegetarian or vegan diet (product contains animal-derived collagen)
04

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
125 participants (estimated)

Study arms

  • Experimental
    Collagen Peptides

    Participants receive daily oral supplementation with specific collagen peptides for 24 weeks. Allocation is randomized 1:1 and double-blinded against placebo. Study visits occur at baseline (T0), 3 months (T1), and 6 months (T2). Blood samples are collected to assess telomere length (qPCR T/S ratio) and telomerase activity (TRAP), alongside inflammation and redox markers. Body composition (bioelectrical impedance), functional tests (muscle strength, mobility), and questionnaires on health and vitality are also performed. The intervention aims to test whether six months of collagen peptides stabilize or extend telomeres and increase telomerase activity compared with placebo.

    Dietary Supplement: Collagen peptides

  • Placebo comparator
    Maltodextrin

    Participants receive a daily placebo matched in a double-blind design for 24 weeks, with the same schedule of study visits at T0, T1, and T2 and the same assessments (blood biomarkers of telomere biology, inflammation/redox; body composition; functional tests; questionnaires) as the verum arm. Maltodextrin serves as the control to compare effects against collagen peptides in a randomized, double-blind, placebo-controlled, parallel-group trial.

    Dietary Supplement: Maltodextrin (Placebo)

Interventions

  • Dietary supplementCollagen peptides

    Collagen peptides (oral daily supplementation), taken once daily for 24 weeks in a randomized 1:1, double-blind design; primary outcomes: telomere length (qPCR T/S) and telomerase activity (TRAP), with inflammatory/redox markers as secondary endpoints. Target population: adults 50-70 years with BMI 25-30 and low-to-moderate activity; vegetarians/vegans excluded due to animal-derived collagen. Matched maltodextrin placebo, identical dosing and visit schedule (T0, T1, T2), serving as the comparator to isolate collagen peptide effects in the parallel-group, double-blind trial. Products are approved as foods; prior clinical studies reported no substance-related adverse effects.

  • Dietary supplementMaltodextrin (Placebo)

    Placebo instead of the collagen peptides

05

What researchers measure

Primary outcomes

  1. Telomere length

    Changes in leukocyte telomere length (qPCR) from peripheral blood

    Time frame: Baseline and after supplementation (24 weeks)

  2. Telomerase Activity

    Changes telomerase activity measured via TRAP Assay from peripheral blood

    Time frame: Baseline and at the end of supplemention (24 weeks)

  3. Change from baseline in DNA-oxidation markers

    Change in DNA Damage measured through comet assay

    Time frame: Baseline and at the end of supplementation (24 weeks)

  4. Change from baseline in micronuclei

    Change in Micronulei measured through CBMN-Assay

    Time frame: Baseline and at the end of supplementation (24 weeks)

Secondary outcomes

  1. Change from baseline in Inflammatory markers

    Changes in plasma concentrations of interleukins like IL-6, IL-10, TNF-alpha

    Time frame: Baseline and at the end of supplemention (24 weeks)

  2. Change from baseline in the redox/antioxidant status

    Change in superoxide dismutase and glutathione peroxidase via enzymatic tests to assess oxidative stress

    Time frame: Baseline and at the end of supplementation (24 weeks)

  3. Change from baseline in body composition

    Change in fat-free mass and fat mass in kg by bioelectrical impedance

    Time frame: Basline, after 3 months and at the end of the supplementation (24 weeks)

  4. Change from baseline metabolic markers

    Change in serum lipid profile and fasting glucose in mg/dL

    Time frame: Baseline and at the end of supplementation (24 weeks)

  5. Change from baseline in hormonal markers

    Change in serum IGF-1and DHEA in ng/mL measured through immunoassays

    Time frame: Baseline and at the end of supplementation (24 weeks)

  6. Change from baseline in muscle strength

    Change in maximal handgrip and leg strength assessed by dynamometry and leg press

    Time frame: Baseline, after 3 months and at the end of supplementation (24 weeks)

  7. Change from baseline in dietary intake

    Change in dietary intake from standardized 3-day food records to contextualize biomarker and functional outcomes

    Time frame: Baseline, after 3 months and at the end of supplementation (24 weeks)

  8. Change from baseline in patient-reported outcomes like quality of life

    Change in health-related quality of life, measured through WHOQOL questionnaire

    Time frame: Baseline, after 3 months and at the end of supplementation (24 weeks)

  9. Change of phase angle

    Change in phase angle by bioelectrical impedance

    Time frame: Basline, after 3 months and at the end of the supplementation (24 weeks)

  10. Change from baseline in Insulin

    Time frame: Baseline and at the end of supplementation (24 weeks)

  11. Change from baseline in patient-reported outcomes like sleep quality

    Change in health-related sleep quality meausred through Pittsburgh Sleep Quality Index questionnaire

    Time frame: Baseline, after 3 months and at the end of supplementation (24 weeks)

  12. Change from baseline in patient-reported outcomes like health

    Change in health measured through PHQ-9 questionnaire

    Time frame: Baseline, after 3 months and at the end of supplementation (24 weeks)

  13. Change from baseline in patient-reported outcomes like fatigue

    Change in health- related outcomes like fatigue measured through FAS questionnaire

    Time frame: Baseline, after 3 months and at the end of supplementation (24 weeks)

  14. Change from baseline in oxidative stress

    Change in glutathione (GSH) and glutathione disulfide (GSSG)

    Time frame: Baseline and at the end of supplementation (24 weeks)

06

Study locations

1 of 1 sites recruiting
  • University of Vienna, NuTraLab
    Vienna, State of Vienna 1070, Austria
    Recruiting
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07456449
Lead sponsor
University of Vienna
Collaborators
Collagen Research Institute
Responsible party
Daniel König (Univ. Professor Dr., University of Vienna) — Principal investigator
First posted
Mar 6, 2026
Start date
Apr 22, 2026
Primary completion
Feb 2028 (estimated)
Completion
Aug 2028 (estimated)
Last update
May 5, 2026

Study contacts

Daniel König, Univ. Prof. Dr.
Contact
daniel.koenig@univie.ac.at
+43-1-4277-59130

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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