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

Mekelle University

Status: Completed

Conditions: Hypertension

Treatments: Other: Aerobic and resistance exercise; Other: Aerobic exercise .; Other: Resistance exercise

Study type: Interventional

Funder types: Other

Identifiers

NCT03029767

213.55.94.37

Details and patient eligibility

About

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.

Full 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).

Enrollment: 92 patients

Sex: All

Ages: 31 to 45 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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92 participants in 4 patient groups

Aerobic exercise

Experimental group

Description:

Aerobic exercise training will be carried out as an intervention activity

Treatment:

Other: Aerobic exercise .

Resistance exercise

Experimental group

Description:

Resistance exercise training will be conducted as an intervention activity

Treatment:

Other: Resistance exercise

Aerobic and resistance exercise

Experimental group

Description:

Aerobic and resistance training will be implemented

Treatment:

Other: Aerobic and resistance exercise

Control group

No Intervention group

Description:

standard or usual activity carried out.Additional intervention will not be given.