- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07412639
Tabata Exercise on Nitric Oxide Synthases and Maresin
Differential Effects of Tabata Exercise on Nitric Oxide Synthases and Maresin in Smokers and Non-Smokers
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Yakutiye
-
Erzurum, Yakutiye, Turkey (Türkiye)
- Ataturk University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age between 18 and 40 years
- No regular participation in structured physical exercise for at least 6 months prior to enrollment
- Absence of any acute or chronic inflammatory disease at baseline
- No history of cardiovascular, metabolic, pulmonary, or neurological disorders
- Ability to comply with the study protocol and complete the tabata exercise program
- Provision of written informed consent
Exclusion Criteria:
- Initiation or cessation of smoking during the study period
- Use of anti-inflammatory, antioxidant, corticosteroid, or vasoactive medications
- Acute infection, surgical intervention, or major trauma within the preceding 3 months
- Diagnosis of diabetes mellitus, hypertension, coronary artery disease, or chronic pulmonary disease
- History of alcohol or substance abuse
- Pregnancy or breastfeeding
- Musculoskeletal or orthopedic conditions that could limit participation in tabata exercise
- Inability to adhere to the exercise protocol or failure to complete follow-up assessments
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Smoker
|
The Tabata protocol consisted of 20-second high-intensity intervals exceeding 70 % of VO₂max and approaching ~90 % of VO₂max, followed by 10 seconds of rest, repeated for 4 minutes per set. Exercises included high knees, froggers, speed skaters, jumping jacks, and mountain climbers. Following the original Tabata design [29], each work-rest cycle was repeated eight times. Each training session began with a 10-15 minute warm-up and concluded with a 10-15 minute cool-down. The total number of sets ranged from 1 to 4, and the number of exercises per session ranged from 4 to 8. Training intensity progressively increased from 30 % to 89 % of maximal effort according to the principle of progressive overload. |
|
Active Comparator: Nonsmoker
|
The Tabata protocol consisted of 20-second high-intensity intervals exceeding 70 % of VO₂max and approaching ~90 % of VO₂max, followed by 10 seconds of rest, repeated for 4 minutes per set. Exercises included high knees, froggers, speed skaters, jumping jacks, and mountain climbers. Following the original Tabata design [29], each work-rest cycle was repeated eight times. Each training session began with a 10-15 minute warm-up and concluded with a 10-15 minute cool-down. The total number of sets ranged from 1 to 4, and the number of exercises per session ranged from 4 to 8. Training intensity progressively increased from 30 % to 89 % of maximal effort according to the principle of progressive overload. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
serum inducible nitric oxide synthase (iNOS) level
Time Frame: 6 week after exercise
|
iNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
|
6 week after exercise
|
|
serum inducible nitric oxide synthase (iNOS) level
Time Frame: 12 week after exercise
|
iNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
|
12 week after exercise
|
|
serum endothelial nitric oxide (eNOS) synthase level
Time Frame: 6 week after exercise
|
eNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
|
6 week after exercise
|
|
serum endothelial nitric oxide (eNOS) synthase level
Time Frame: 12 week after exercise
|
eNOS level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
|
12 week after exercise
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
serum maresin level
Time Frame: 6 week after exercise
|
Maresin level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
|
6 week after exercise
|
|
serum maresin level
Time Frame: 12 week after exercise
|
Maresin level were quantified using immunosorbent assay (ELISA) kits, according to the manufacturers' instructions.
|
12 week after exercise
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Ding N, Sang Y, Chen J, Ballew SH, Kalbaugh CA, Salameh MJ, Blaha MJ, Allison M, Heiss G, Selvin E, Coresh J, Matsushita K. Cigarette Smoking, Smoking Cessation, and Long-Term Risk of 3 Major Atherosclerotic Diseases. J Am Coll Cardiol. 2019 Jul 30;74(4):498-507. doi: 10.1016/j.jacc.2019.05.049.
- Fysikopoulos A, Seimetz M, Hadzic S, Knoepp F, Wu CY, Malkmus K, Wilhelm J, Pichl A, Bednorz M, Tadele Roxlau E, Ghofrani HA, Sommer N, Gierhardt M, Schermuly RT, Seeger W, Grimminger F, Weissmann N, Kraut S. Amelioration of elastase-induced lung emphysema and reversal of pulmonary hypertension by pharmacological iNOS inhibition in mice. Br J Pharmacol. 2021 Jan;178(1):152-171. doi: 10.1111/bph.15057. Epub 2020 Apr 28.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ATAUNISPORT1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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