Skip to main content
Clinical Trials/NCT07370363
NCT07370363
Not yet recruiting
Not Applicable

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

Havva Talay Çalış1 site in 1 country42 target enrollmentStarted: February 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Havva Talay Çalış
Enrollment
42
Locations
1
Primary Endpoint
Serum Sestrin-2 Level

Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
30 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

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

Arms & Interventions

Moderate-Intensity Continuous Exercise

Experimental

Participants perform supervised moderate-intensity continuous aerobic exercise at a prescribed intensity and frequency.

Intervention: Moderate-Intensity Continuous Exercise (Behavioral)

Brisk Interval Exercise

Experimental

Participants perform supervised interval aerobic exercise consisting of alternating bouts of higher and moderate intensity.

Intervention: Brisk Interval Exercise (Behavioral)

Outcomes

Primary Outcomes

Serum Sestrin-2 Level

Time Frame: Baseline and end of 8-week intervention

Serum Sestrin-2 levels will be measured using enzyme-linked immunosorbent assay (ELISA). Blood samples will be collected 48 hours before the start of the 8-week exercise program and 48 hours after completion of the intervention in order to avoid the acute effects of exercise. The primary outcome is the change in Sestrin-2 levels from baseline to post-intervention.

Maximal Oxygen Consumption (VO2max)

Time Frame: Baseline and end of 8-week intervention

VO2max will be assessed using cardiopulmonary exercise testing (CPET) according to standardized protocols. Measurements will be performed before the start of the exercise program and after completion of the 8-week intervention. The change in VO2max from baseline to post-intervention will be analyzed.

Secondary Outcomes

  • Lipid Profile(Baseline and end of 8-week intervention)
  • Insulin Resistance(Baseline and end of 8-week intervention)
  • Functional Capacity(Baseline and end of 8-week intervention)
  • Blood Pressure(Baseline and end of 8-week intervention)
  • Change in body weight(Baseline and Week 8)
  • Change in body mass index (BMI)(Baseline and Week 8)
  • Change in waist circumference(Baseline and Week 8)
  • Change in International Physical Activity Questionnaire (IPAQ) score(Baseline and Week 8)
  • Change in Hospital Anxiety and Depression Scale (HADS) scores(Baseline and Week 8)

Investigators

Sponsor
Havva Talay Çalış
Sponsor Class
Other Gov
Responsible Party
Sponsor Investigator
Principal Investigator

Havva Talay Çalış

Professor of Physical Medicine and Rehabilitation

Kayseri City Hospital

Study Sites (1)

Loading locations...

Similar Trials