Fact CheckerSign in

NCT06845436Recruiting

Effects of Combined High Intensity Interval Training and Resistance Training

Effects of Combined High Intensity Interval Training and Resistance Training on Body Composition, Blood Pressure, and Cardiorespiratory Fitness in Obese Hypertensive Men

Source: ClinicalTrials.gov · Last updated 4 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Background: Hypertension has long been considered as a major risk factor for cardiovascular disease representing a high public health concern. Objectives: the purpose of this study is to evaluate the effects of combined HIIT and resistance training on body composition, blood pressure, and cardiorespiratory fitness in obese hypertensive men. Methods: This study will make use of sixty obese hypertensive men aged 40 to 60 years. All participants meeting the eligibility criteria will be assigned to one of three groups; combined HIIT and resistance group, HIIT only group or control group. Combined exercise group subjects will undergo weekly three sessions of both HIIT and resistance training for sixteen weeks. The HIIT session will involve four four-minute high-intensity intervals with an intensity of at 80-95% of the HRmax interspersed with two-minute active recovery intervals with intensity of 40% to 60% of the HRmax. The resistance training session will be composed of eight exercises perform 3 sets of 8-12 repetitions with an intensity of 80% of the subject's estimated 1-RM. The HIIT only group perform 12 weeks of HIIT only. The control group subjects will be instructed not to change their usual daily physical activities routine and instructed to abstain from practicing any exercise regimens during the 12-week study period. Body composition measures, blood pressure and VO2peak will be assessed at baseline and at the end of the study period. Results: All the outcome variables will be assessed at baseline and 12 weeks following the treatment period.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
20 Feb 2025
Start date
1 Apr 2025
Primary completion date
1 Jul 2025
Lead sponsor
Prince Sattam Bin Abdulaziz University
NCT number
NCT06845436

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 1 Apr 2025 to the primary completion date, 1 Jul 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • diabetes mellitus
  • a history of respiratory or chronic heart disease

Other

  • musculoskeletal problems that may limit their ability to participate in resistance or HIIT programs

Who the study is looking for

  • men aged between 40 and 60 years old,
  • have been diagnosed with clinical stage 1 or 2 hypertension,
  • being obese with body mass index more than 30 kg/m2
  • physically inactive

Age in the registry: 40 years to 60 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Prince Sattam bin Abdulaziz University
Coordinator of this site? Confirm its status
RiyadhSaudi ArabiaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.