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Not yet recruiting NCT07370363

Exercise Effects on Cardiometabolic Health and Sestrin-2 in Hypertensive Obese Women

No phase Interventional Obesity Hypertension

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In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Moderate-Intensity Continuous Exercise, Brisk Interval Exercise.
Who it may be relevant to
Registry conditions: Obesity, Hypertension. Basic parameters: 30 years — 65 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effects of Moderate-Intensity Continuous Exercise Versus Brisk Interval Exercise on Cardiometabolic Parameters and Sestrin-2 Levels in Hypertensive Obese Women: A Randomized Controlled Trial

Overview

Obesity is a chronic and complex disease characterized by excessive fat accumulation that adversely affects health and quality of life. It is commonly accompanied by low-grade chronic systemic inflammation, which contributes to the development of insulin resistance, type 2 diabetes, dyslipidemia, hypertension, and cardiovascular diseases. Hypertension is highly prevalent among individuals with obesity, and excess body weight is a major contributor to elevated blood pressure and related cardiometabolic risk. Regular aerobic exercise is a cornerstone of non-pharmacological management for both obesity and hypertension and has been shown to reduce chronic inflammation by downregulating pro-inflammatory pathways and upregulating anti-inflammatory mechanisms. Sestrin-2, a stress-responsive protein encoded by the SESN2 gene, has been proposed as an important regulator of metabolic homeostasis and inflammation through activation of the AMPK pathway and inhibition of NF-κB signaling. However, evidence regarding the effects of different exercise modalities on circulating Sestrin-2 levels in hypertensive obese individuals remains limited. This prospective, randomized controlled trial aims to compare the effects of two different aerobic exercise protocols on serum Sestrin-2 levels, inflammatory status, and cardiometabolic parameters in hypertensive obese women. Cardiopulmonary exercise testing will be used to comprehensively assess cardiorespiratory fitness and physiological responses to exercise. The results of this study are expected to contribute to a better understanding of exercise-induced anti-inflammatory mechanisms and to support the development of safe, effective, and applicable exercise prescriptions for hypertensive obese women.

Detailed description

Obesity is a chronic disease associated with excessive adipose tissue accumulation and a persistent low-grade inflammatory state, which contributes to the development of cardiometabolic disorders such as hypertension, insulin resistance, dyslipidemia, and cardiovascular disease. In women, the coexistence of obesity and hypertension substantially increases morbidity and negatively affects functional capacity and quality of life. Exercise training is a cornerstone of lifestyle-based management; however, the optimal characteristics of aerobic exercise prescription and its effects on emerging molecular biomarkers remain incompletely understood.

Sestrin-2 is a stress-inducible protein encoded by the SESN2 gene and has been implicated in metabolic regulation through activation of the AMP-activated protein kinase pathway and suppression of inflammatory signaling pathways, including nuclear factor kappa B. Experimental and clinical evidence suggests that Sestrin-2 may play a protective role against obesity-related inflammation and metabolic dysfunction. Nevertheless, data regarding the modulation of circulating Sestrin-2 levels in response to different aerobic exercise modalities in hypertensive obese women are limited.

This study is designed as a prospective, randomized controlled trial including hypertensive obese women who meet predefined eligibility criteria. Participants are randomly allocated to one of two supervised aerobic exercise intervention groups: moderate-intensity continuous exercise or brisk interval exercise. Both interventions are conducted for a predefined training period under standardized conditions.

Cardiopulmonary exercise testing is performed to assess cardiorespiratory fitness and physiological responses to exercise, including maximal oxygen consumption. Blood samples are collected to measure serum Sestrin-2 levels and cardiometabolic parameters. Additional assessments include lipid profile, indices of insulin resistance, anthropometric measurements, functional capacity evaluated by the six-minute walk test, and patient-reported questionnaire outcomes.

The primary outcome measures of the study are changes in serum Sestrin-2 levels and maximal oxygen consumption. Secondary outcome measures include changes in cardiometabolic risk factors, functional capacity, and anthropometric parameters. The findings of this study are expected to provide insight into exercise-induced anti-inflammatory mechanisms and to inform evidence-based aerobic exercise prescriptions for hypertensive obese women.

Interventions

  • Behavioral Moderate-Intensity Continuous Exercise
    Supervised moderate-intensity continuous aerobic exercise performed at a prescribed intensity and frequency for the duration of the intervention period.
  • Behavioral Brisk Interval Exercise
    Supervised interval aerobic exercise consisting of alternating bouts of higher and moderate intensity performed throughout the intervention period.

Primary outcome measures

  • Serum Sestrin-2 Level [Time frame: Baseline and end of 8-week intervention]
  • Maximal Oxygen Consumption (VO2max) [Time frame: Baseline and end of 8-week intervention]
Secondary outcome measures (9)
  • Lipid Profile [Time frame: Baseline and end of 8-week intervention]
  • Insulin Resistance [Time frame: Baseline and end of 8-week intervention]
  • Functional Capacity [Time frame: Baseline and end of 8-week intervention]
  • Blood Pressure [Time frame: Baseline and end of 8-week intervention]
  • Change in body weight [Time frame: Baseline and Week 8]
  • Change in body mass index (BMI) [Time frame: Baseline and Week 8]
  • Change in waist circumference [Time frame: Baseline and Week 8]
  • Change in International Physical Activity Questionnaire (IPAQ) score [Time frame: Baseline and Week 8]
  • Change in Hospital Anxiety and Depression Scale (HADS) scores [Time frame: Baseline and Week 8]

Eligibility criteria

Inclusion criteria

  • Female participants aged between 30 and 65 years
  • Body mass index between 30.0 and <40.0 kg/m² (Class I and Class II obesity)
  • Diagnosis of hypertension according to the 2018 European Society of Hypertension/European Society of Cardiology (ESH/ESC) guidelines
  • Sedentary lifestyle, defined as total weekly exercise duration of less than 60 minutes
  • Medically eligible for exercise participation, with approval from a Physical Medicine and Rehabilitation specialist and an Internal Medicine specialist
  • Willingness to participate in the study and provision of written informed consent

Exclusion criteria

  • Neuromuscular disorders, uncontrolled psychiatric diseases, or cognitive impairment limiting exercise participation
  • Congestive heart failure, unstable angina, or acute cardiac conditions including acute myocardial infarction, acute endocarditis, myocarditis, or pericarditis
  • Presence of uncontrolled systemic diseases, including:
  • Uncontrolled hypertension
  • Uncontrolled diabetes mellitus
  • Chronic liver failure
  • Chronic kidney disease or patients receiving dialysis
  • Chronic obstructive pulmonary disease or asthma
  • History or presence of malignancy
  • Acute infection at the time of enrollment
  • Acute peripheral vascular disease
  • Symptomatic severe aortic stenosis
  • Acute pulmonary embolism or pulmonary infarction
  • Use of systemic corticosteroids or immunosuppressive medications
  • Inability to comply with the study protocol or lack of cooperation
  • Refusal to participate in the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Turkey (Türkiye) · 1 center
  • Kayseri City Hospital — Kayseri

Publications

  • Lee JH, Budanov AV, Karin M. Sestrins orchestrate cellular metabolism to attenuate aging. Cell Metab. 2013 Dec 3;18(6):792-801. doi: 10.1016/j.cmet.2013.08.018. Epub 2013 Sep 19. PMID 24055102
  • Williams B, Mancia G, Spiering W, Agabiti Rosei E, Azizi M, Burnier M, Clement DL, Coca A, de Simone G, Dominiczak A, Kahan T, Mahfoud F, Redon J, Ruilope L, Zanchetti A, Kerins M, Kjeldsen SE, Kreutz R, Laurent S, Lip GYH, McManus R, Narkiewicz K, Ruschitzka F, Schmieder RE, Shlyakhto E, Tsioufis C, Aboyans V, Desormais I; ESC Scientific Document Group. 2018 ESC/ESH Guidelines for the management PMID 30165516

Identifiers

NCT: NCT07370363 · KayseriCHsestrin2

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗