Clinical trial Recruiting at 1 site Interventional Ages 18 to 40

Concurrent exercise program changes PCSK9 in adults with overweight

Official title: Effects of Concurrent Training on Serum PCSK9 Levels in Adults With Overweight: A Randomized Controlled Trial

Run by Kastamonu University · NCT07910916 · Data updated 2026-11-12

A supervised program of aerobic plus resistance training for eight weeks will test whether it lowers PCSK9 levels in adults who are overweight.

Quick facts

Study typeInterventional
Ages18 Years to 40 Years
SexAll
Enrollment42 (estimated)
SponsorKastamonu University
Academic / other
Locations1 site (Çatalzeytin, Kastamonu)
StatusRecruiting
StartedNovember 2, 2026
Main results expectedDecember 30, 2027
Study endsMay 30, 2028
Registry record updatedNovember 3, 2026
Trial IDNCT07910916 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults 18-40 years with BMI 25.0–29.9 kg/m² who are not regularly exercising and do not have major cardiovascular or metabolic diseases.

Probably not a fit

Individuals with cardiovascular disease, diabetes, recent weight loss, or medications affecting PCSK9 may not experience benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study will enroll 42 adults aged 18-40 with BMI 25.0–29.9 and randomly assign them to either a supervised concurrent exercise program three days per week for eight weeks or to continue usual activities. The program includes about 60 minutes per session of aerobic and resistance training with warm-up and cool-down. Researchers will measure serum PCSK9, lipid profiles, glucose, and body composition before and after the intervention to see how exercise affects cholesterol regulation. The study will also explore how PCSK9 relates to changes in body composition. The lead sponsor is Kastamonu University and the study will take place at Kastamonu University facilities in Turkey.

Why it matters

Potential benefit: If successful, the program could show a practical way to influence cholesterol regulation through combined exercise.

How similar studies have gone: Earlier work has shown mixed effects of exercise on PCSK9, so this study adds clarity with a controlled design.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adults aged 18-40 years.
* Body mass index (BMI) between 25.0 and 29.9 kg/m².
* No participation in a regular exercise program during the previous two months (3-5 days per week, totaling 150 minutes per week).

Exclusion Criteria:

* Diagnosed coronary artery disease, heart failure, hypertension, diabetes mellitus, or other chronic cardiovascular or metabolic diseases.
* Acute or chronic inflammatory disease or active infection.
* History of malignancy or active cancer.
* Neurological, orthopedic, or musculoskeletal conditions that prevent participation in physical exercise.
* Current use of antihypertensive, lipid-lowering, antidiabetic, systemic glucocorticoid, or other medications that may affect PCSK9 levels.
* Current smoking or use of other tobacco products.
* Pregnancy or breastfeeding.
* Loss of 5% or more of body weight during the previous three months or participation in a weight-loss diet.
* Bariatric surgery or use of pharmacological weight-management treatment during the previous three months.

Where it's running

  • Kastamonu University, Çatalzeytin Vocational School
    Çatalzeytin, Kastamonu, Turkey (Türkiye)
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.