← Back to Clinical Trials
Recruiting NCT07833956

NCT07833956 Circadian Rhythm and Cardiovascular Recovery After Submaximal Exercise

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07833956
Status Recruiting
Phase —
Sponsor Saglik Bilimleri Universitesi
Condition Circadian Rhythm
Study Type OBSERVATIONAL
Enrollment 124 participants
Start Date 2026-10-01
Primary Completion 2027-03-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 45 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 124 participants in total. It began in 2026-10-01 with a primary completion date of 2027-03-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This cross-sectional, observational, and analytical study aims to investigate the relationship between morningness-eveningness characteristics and cardiovascular recovery after a submaximal exercise test in healthy individuals aged 18-45 years. Circadian preference will be assessed using the Morningness-Eveningness Questionnaire, sleep quality will be assessed using the Pittsburgh Sleep Quality Index, and cardiovascular recovery will be evaluated following the 6-Minute Walk Test

Eligibility Criteria

Inclusion Criteria: * Aged 18-45 years. * Being healthy. * Voluntarily agreeing to participate in the study. Exclusion Criteria: * Presence of cardiovascular, pulmonary, neurological, or orthopedic disease. * Having a health problem that prevents exercise. * Use of medication that may affect exercise tolerance. * Pregnancy.

Contact & Investigator

Central Contact

Gamze Koyutürk, Asst Prof

✉ gamzealtinkaynak@gmail.com

📞 +905065798671

Principal Investigator

Gamze Koyutürk, Asst Prof

PRINCIPAL INVESTIGATOR

Topkapı University

Frequently Asked Questions

Who can join the NCT07833956 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 45 Years, studying Circadian Rhythm. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07833956 currently recruiting?

Yes, NCT07833956 is actively recruiting participants. Contact the research team at gamzealtinkaynak@gmail.com for enrollment information.

Where is the NCT07833956 trial being conducted?

This trial is being conducted at Istanbul, Turkey (Türkiye).

Who is sponsoring the NCT07833956 clinical trial?

NCT07833956 is sponsored by Saglik Bilimleri Universitesi. The principal investigator is Gamze Koyutürk, Asst Prof at Topkapı University. The trial plans to enroll 124 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology