Fact CheckerSign in

NCT06243224Completed

The Effect Of High Intensity Interval Training And Moderate Intensity Continuous Training In Patients With Hypertension

The Effect Of High Intensity Interval Training And Moderate Intensity Continuous Training On Cardiopulmonary Parameters And Clinical Findings In Patients With Hypertension:A Randomized Comparative Study

Source: ClinicalTrials.gov · Last updated 13 May 2024

Brief summary (registry, in English)

Comparison of high intensity interval training (HIIT) and moderate intensity continuous training (MICT) in patients with hypertension patient in terms of aerobic capacity, blood pressure level, anxiety and depression scores, quality of life, kinesiophobia levels and sleep quality measurement.

Status (registry)
Completed
Study type
Interventional
Enrollment
38 (actual)
First submitted
13 Jan 2024
Start date
15 Apr 2023
Primary completion date
15 Feb 2024
Lead sponsor
Ankara City Hospital Bilkent
NCT number
NCT06243224

What you commit to

  • Study type: Interventional
  • Participants enrolled: 38
  • From 15 Apr 2023 to the primary completion date, 15 Feb 2024
  • 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

  • Clinical heart failure
  • Uncontrolled hypertension
  • Secondary hypertension
  • Moderate or severe pulmoner disease
  • Symptomatic peripheral arterial disease
  • Unstable arrhythmia
  • Unstable or severe angina
  • Moderate or severe valvular heart disease
  • Congenital heart disease
  • Recent history of stroke
  • Diabetes mellitus
  • Severe musculoskeletal disease causing exercise limitation

Other

  • Cognitive limitation unable to understand the research protocol
  • Pace maker presence
  • Language problem
  • Autonomic neuropathy
  • Cardiomyopathy
  • Being unable to continue treatment (3 days a week for 4 weeks)

Who the study is looking for

  • Being diagnosed with Isolated Hypertension
  • Being cognitively competent
  • Being between the ages of 35-55
  • Having given informed consent to participate in the study.

Age in the registry: 35 years to 55 years · Sex: All · 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
Ankara Bilkent City Hospital
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

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