Clinical trial Recruiting at 1 site Observational Ages 18 to 65

How your daily body clock relates to breathing, activity, and nutrition after COVID-19

Official title: Comparison of Respiratory Muscle Strength, Physical Activity Level, and Dietary Habits in Individuals With Post-COVID-19 Syndrome Having Different Circadian Rhythms

Run by Hacettepe University · NCT07545499 · Data updated 2026-11-12

This project tests whether morning, intermediate, or evening circadian types relate to respiratory muscle strength, physical activity, sleep, and eating habits in adults with post-COVID-19 syndrome.

More Post-Acute COVID-19 Syndrome trials

Quick facts

Study typeObservational
Ages18 Years to 65 Years
SexAll
Enrollment50 (estimated)
SponsorHacettepe University
Academic / other
Locations1 site (Ankara, Altindağ)
StatusRecruiting
StartedMay 22, 2025
Main results expectedAugust 22, 2026
Study endsMay 22, 2027
Registry record updatedApril 22, 2026
Trial IDNCT07545499 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18–65 years with a confirmed diagnosis of post-COVID-19 syndrome, PCFS grade 2–3, clinically stable, able to read Turkish, and without uncontrolled comorbidities or mobility-limiting neurological/orthopedic conditions are ideal candidates.

Probably not a fit

Patients with recent major cardiovascular events, severe uncontrolled chronic disease, significant neurological or orthopedic limitations, or inability to complete in-person assessments are unlikely to benefit or be eligible.

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

What this trial studies

This is a cross-sectional observational study enrolling adults aged 18–65 with confirmed post-COVID-19 syndrome to compare respiratory muscle strength, physical activity, nutritional habits, sleep quality, fatigue, and gastrointestinal symptoms across chronotypes (morning, intermediate, evening) defined by the Munich Chronotype Questionnaire. Respiratory function will be measured with maximal inspiratory/expiratory pressures (MIP/MEP), dynamic testing using a POWERbreathe device, and respiratory endurance threshold protocols, while activity and nutrition are captured with validated questionnaires such as the IPAQ. The protocol also includes genetic analysis of CLOCK gene polymorphisms to provide an objective correlate of circadian differences. All testing is performed in person at a single center and participants must be clinically stable and able to complete the assessments.

Why it matters

Potential benefit: If successful, the findings could help tailor rehabilitation and lifestyle recommendations to a patient’s chronotype to improve symptoms and daily functioning after COVID-19.

How similar studies have gone: Early research suggests circadian patterns can affect recovery, activity, and sleep, but applying CLOCK gene analysis specifically to post-COVID-19 outcomes is relatively novel and not yet proven.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Diagnosed with Post-COVID-19 Syndrome
* Aged between 18-65 years
* Able to read and understand Turkish
* Voluntary participation
* Classified as Post-Covid Functional Status Scale (PCFS) grade 2-3
* Clinically stable condition
* No uncontrolled comorbidities (e.g., hypertension, diabetes under control)
* No orthopedic or neurological conditions affecting exercise testing

Exclusion Criteria:

* Recent myocardial infarction or pulmonary embolism
* Severe uncontrolled chronic diseases
* Neurological or orthopedic conditions limiting mobility
* Psychiatric or neurological disorders affecting cooperation or test compliance
* Inability to complete assessments

Where it's running

  • Hacettepe University Faculty of Physical Therapy and Rehabilitation
    Ankara, Altindağ, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

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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.