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Healthy AdultNCT07800156

The Effect of Aerobic Exercise on the Irisin/Klotho/Sirtuin-1/BDNF Axis

A study testing Aerobic exercise in people with Healthy Adult and Athlete, run by Cemre Didem Eyipinar at 1 site in Turkey (Türkiye).

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The purpose of this study is to investigate the effects of an acute aerobic exercise on irisin, klotho, sirtuin-1, and BDNF levels in the healthy adults. The findings will help understand the physiological impacts of exercise on these biomarkers. Read more about this study

Who is it for?
Ages 18 to 45 years, men onlyHealthy volunteers can take part
Conditions the study is for
Healthy Adult, Athlete
What is being tested?
Aerobic exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
26 participants
Where
1 siteTurkey (Türkiye)
Study dates
2 Sep 2026to 2 May 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Being between the ages of 18 and 45
  • Being in good health and having no diagnosis of any chronic disease
  • Not having taken regular medication within the last 4 weeks
  • Voluntary participation and providing written informed consent

Who cannot join

  • Individuals with a history of cardiovascular, endocrine, metabolic, or renal disease
  • Individuals with a history of active infection, musculoskeletal injury, or severe disability
  • Individuals with any medical condition that might prevent participation in exercise
  • Individuals unable to regularly participate in the exercise protocol throughout the study

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Cemre Didem Eyipınar, PhD contact

+90 545 264 54 86

cemreeyipinar@gantep.edu.tr

Turkey (Türkiye)1 site
  • Gaziantep University Faculty of Sports Sciences

    Gaziantep, Sehitkamil, 85142

    CEMRE, 05452645486, cemreeyipinar@gantep.edu.tr

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Aerobic Exercise on the Irisin/Klotho/Sirtuin-1/BDNF Axis: A Randomized Controlled Study

The purpose of this study is to investigate the effects of an acute aerobic exercise on irisin, klotho, sirtuin-1, and BDNF levels in the healthy adults. The findings will help understand the physiological impacts of exercise on these biomarkers.

Being tested
Aerobic exercise

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07800156
Study groupRoleWhat they receive
Experimental GroupExperimentalAerobic exercise
Receives: Behavioral: Aerobic exercise
Control GroupNo interventionNo exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Salivary Irisin Level

    Irisin concentration will be determined from a saliva sample using the ELISA technique.

    Measured: Baseline- immediately after exercise and 1 hours after exercise

  2. Salivary Klotho Level

    Klotho concentration will be determined from a saliva sample using the ELISA technique.

    Measured: Baseline- immediately after exercise and 1 hours after exercise

  3. Salivary Sirtuin Level

    Sirtuin concentration will be determined from a saliva sample using the ELISA technique.

    Measured: Baseline- immediately after exercise and 1 hours after exercise

  4. Salivary BDNF Level

    BDNF concentration will be determined from a saliva sample using the ELISA technique.

    Measured: Baseline- immediately after exercise and 1 hours after exercise

Secondary outcomes (1)
  1. Saliva Flow Rate

    It will be calculated individually by dividing the weight of the saliva collected within one minute by the duration.

    Measured: Baseline- İmmediately after exercise and 1 hour after exercise

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Sep 2026
  2. Study start2 Sep 2026 (estimated)
  3. Primary completion2 Apr 2027 (estimated)
  4. Study completion2 May 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
26 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07800156
Sponsor's protocol ID
KAEK-120
Status last verified
Aug 2026
First submitted
28 Aug 2026
Last updated
2 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Aerobic exercise in people with Healthy Adult and Athlete, run by Cemre Didem Eyipinar at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 2 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Cemre Didem Eyipınar, PhD (+90 545 264 54 86, cemreeyipinar@gantep.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Salivary Irisin Level (time frame: Baseline- immediately after exercise and 1 hours after exercise). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Sep 2026.

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