Effect of Exercise on Selected Anthropometric,Biochemical and Physiological Variables Among Hypertensive Patients

Not Applicable

Completed

• Conditions: Hypertension
• Interventions: Other: Aerobic and resistance exercise; Other: Aerobic exercise .; Other: Resistance exercise

• Registration Number: NCT03029767
• Lead Sponsor: Mekelle University

Brief Summary

Hypertension is the most common risk factor for development of stroke, congestive heart failure chronic kidney disease, and coronary artery disease in Sub Saharan Africa. The prevalence of hypertension will increase by 2025 in most parts of the world including Ethiopia according to World Health Organization.

Physical inactivity has been identified as a stronger predictor of chronic diseases such as hypertension. Exercise as a lifestyle modification is beneficial to a wide variety of health conditions, specific to hypertension; the benefits of exercise have been promoted by a number of organizations and agencies including World Health Organization.

According to the knowledge of the investigator there are no research works in relation to aerobic and resistance exercise effects among hypertensive patients generally in Ethiopia, and particularly in the area selected for the present research. Therefore the aim of this study is to assess the effect of aerobic and resistance exercises on selected anthropometric, biochemical and physiological variables among hypertensive patients in Hawassa University Referral Hospital.

Detailed Description

For eligible participants the requirements of the study will be explained and agree voluntarily to undergo the training and testing program. During orientation for each participant the risks, purpose, procedures and confidentiality of the requirement of the experiment testing as well as training protocol will be explained thoroughly prior to their written informed consent in their local language, and they have a full right to refuse from participating in this research or they have also the full right to withdraw from this study at any time they wish.

After acquisition of informed consent and exclusion criteria eligible participants will be randomized to one of four groups. Sequence allocation will be done by an individual who do not know and have no contact with the study participants .

Statistical analyses will be done using Statistical Package for Social Science (SPSS Version 20). One-way analyses of variance (ANOVA) will be used to assess differences between initial values of the four groups on all the variables measured. In addition, the effect of the experimental treatments on the anthropometric, biochemical and physiological variables will be examined by using two-way analysis of variance (ANOVA).

Study Timeline

• Study First Submitted: 2017-01-20
• Study First Submitted QC: 2017-01-20
• Study First Posted: 2017-01-24
• Study Start: 2017-02-20
• Primary Completion: 2017-06-17
• Study Completion: 2017-06-17
• Status Verified: 2018-11
• Last Update Submitted: 2018-11-22
• Last Update Posted: 2018-11-26

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 92

Inclusion Criteria

• Hypertensive patients who will give a written consent to participate in the study
• Hypertensive patients who are going to stay in the area throughout the study period
• Hypertensive patients between the age range of 31 and 45 years old with essential mild hypertension (systolic blood pressure between 140-159 mmHg and diastolic blood pressure between 90 and 99 mm Hg)
• participants not participated in structured physical exercises for previous 3 months
• patients who are on single anti-hypertensive medication or unmedicated
• Body mass index(BMI) 18.5kg/m2-29.9kg/m2

Exclusion Criteria

• participants who involved in any exercise program prior to study
• pregnant women
• women who are taking contraceptive drugs
• Participants who are taking lipid lowering drugs
• participants who are taking any medications except single anti-hypertensive medication
• participants with organ damage,
• secondary hypertension
• patients with known liver problem
• patients with renal disease ,heart disease, brain disease
• participants with age less than 31 and greater than 45 years
• diabetic patients

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Aerobic and resistance exercise	Aerobic and resistance exercise	Aerobic and resistance training will be implemented
Aerobic exercise	Aerobic exercise .	Aerobic exercise training will be carried out as an intervention activity
Resistance exercise	Resistance exercise	Resistance exercise training will be conducted as an intervention activity

Primary Outcome Measures

Name	Time	Method
Effect of aerobic exercise training (as intervention measures) on resting systolic blood pressure will be assessed.	[ Time Frame: sixteen weeks ]	Change rates of systolic blood pressure among intervention and control groups

Secondary Outcome Measures

Name	Time	Method
Effect of combined aerobic and resistance training on the reduction of body mass index among the hypertensive patients will be assessed	[ Time Frame: Sixteen weeks ]	Body mass index reduction changes among intervention and control groups
Effect of combined aerobic and resistance training on the increasement of HDL-c level among the hypertensive patients will be assessed	[ Time Frame: Sixteen weeks ]	HDL-C level changes among intervention and control groups

Trial Locations

Locations (1)

Hawassa University Referral Hospital; 🇪🇹 Hawassa, Southern Nations Nationality Peoples Region, Ethiopia