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Effect of Aerobic Exercise in Patients With Essential Hypertension

Completed
Conditions
Aerobic Exercise
Essential Hypertension
Interventions
Other: Supervised Aerobic Exercise
Registration Number
NCT05987436
Lead Sponsor
TC Erciyes University
Brief Summary

The goal of this observational study is to evaluate the effects of a supervised aerobic exercise training program on weight loss, functional capacity, quality of life (QoL), and depression levels in patients with essential hypertension.

Detailed Description

Patients who chose the treatment type according to personal preferences were divided into two groups: Group 1(n:91) exercised for six weeks, five sessions per week under the supervision of a medical doctor in the aerobic exercise laboratory, and group 2(n:47) was advised to maintain dietary habits and physical activity levels. Body weight, serum lipid levels, functional capacity, QoL, and depression level of all the participants were evaluated at baseline and 6 weeks later.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
138
Inclusion Criteria
  • Over 18 years of age,
  • Absence of concomitant other metabolic and cardiovascular diseases.
Exclusion Criteria
  • Having suffered an event of ischaemic heart disease (<6 months),
  • Secondary hypertension,
  • Hypertrophic obstructive cardiomyopathy,
  • Congestive heart failure,
  • Uncontrolled cardiac arrhythmia,
  • Thyroid dysfunction,
  • Diabetes mellitus,
  • Symptomatic peripheral arterial occlusive disease,
  • Aortic insufficiency or stenosis,
  • Pulmonary or heart disease with dyspnoea at small or moderate effort,
  • An outbreak of orthopedic problems on hip, knee or ankles, such as arthroplasty, contracture or severe osteoarthritis,
  • Using of antidepressant or anxiolytic drugs,
  • Pregnancy,
  • Cognitive disfunction.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Group 1Supervised Aerobic ExerciseGroup 1 exercised for six weeks, involving once per day, five sessions per week under the supervision of a medical doctor, and a nurse in the aerobic exercise laboratory. The aerobic exercise training program lasted six weeks, and patients lived in the hospital for the whole period. Aerobic exercise training was performed on cycle ergometers (Ergoline, ergoselect II 100/200/Reha, Germany) equipped with a computed ergometer and developed to monitor electrocardiography (ECG), heart rhythm, and BP. Each session consisted of a 5-minute warm-up, followed by 50 minutes of aerobic exercise with an intensity of 50% to 70% of heart rate reserve, calculated by Karvonen formula, and ended with a 5-min cool-down period.
Primary Outcome Measures
NameTimeMethod
The functional capacity6MWT was assessed in face-to-face interviews before and immediately after the treatment was completed.

The 6MWT test and the estimated metabolic equivalents or METs were used performed to evaluate functional capacity.

Body weightwas measured at the pre-treatment period and the post-treatment 6th week for all the participants by the same physician.

kilograms

Quality of LifeSF36 was assessed in face-to-face interviews before and immediately after the treatment was completed.

Quality of life was assessed with Short Form-36 (SF-36).

Blood samplesTwelve-hour fasting blood samples were collected between 6.00 am, and 10.00 am at baseline and week 6.

Serum total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, very-low-density lipoprotein (VLDL) cholesterol, and triglycerides

Depression levelBDI was assessed in face-to-face interviews before and immediately after the treatment was completed.

Depression level was assessed Beck Depression Inventory (BDI).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Selcuk University Faculty of Medicine

🇹🇷

Konya, Turkey

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