Pre Hypertension Clinical Trial
Official title:
Effects of Life Style Intervention Manual on Metabolic, Cardiovascular, Respiratory and Physical Parameters in Pre Hypertensive Sedentary Population
Verified date | April 2024 |
Source | Riphah International University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Hypertension is an increasingly important medical and public health issue. The prevalence of hypertension increases with advancing age to the point where more than half of people 60-69 years of age and approximately three-fourths of those 70 years of age and older are affected. The age related rise in SBP is primarily responsible for an increase in both incidence and prevalence of hypertension with increasing age. At present, it is estimated that about 1 billion people worldwide have hypertension (>140/90 mmHg), and this number is expected to increase to 1.56 billion by 2025. Because of the new data on lifetime risk of hypertension and the impressive increase in the risk of cardiovascular complications associated with levels of BP previously considered to be normal, the JNC 7 report has introduced a new classification that includes the term "prehypertension" for those with BPs ranging from 120-139 mmHg systolic and/or 80-89 mmHg diastolic. This new designation is intended to identify those individuals in whom early intervention by adoption of healthy lifestyles could reduce BP, decrease the rate of progression of BP to hypertensive levels with age, or prevent hypertension entirely. Prehypertension is not a disease category. Rather, it is a designation chosen to identify individuals at high risk of developing hypertension, so that both patients and clinicians are alerted to this risk and encouraged to intervene and prevent or delay the disease from developing. Individuals who are pre hypertensive are not candidates for drug therapy based on their level of BP and should be firmly and unambiguously advised to practice lifestyle modification in order to reduce their risk of developing hypertension in the future. The goal for individuals with prehypertension and no compelling indications is to lower BP to normal levels with lifestyle changes, and prevent the progressive rise in BP using the recommended lifestyle modifications.
Status | Completed |
Enrollment | 240 |
Est. completion date | December 30, 2023 |
Est. primary completion date | November 30, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years to 40 Years |
Eligibility | Inclusion Criteria: 1. Aged between 25 - 40 years 2. Either gender 3. Clinic BP will be consistent with the diagnosis of pre-hypertension 4. Sedentary Subjects (<150 min/week or <600 MET-min/week on IPAQ Urdu Version) Exclusion Criteria: 1. Body Mass Index less than 18.5 kg/m2 or greater than 45 kg/m2 2. Evidence of target organ damage such as left ventricular hypertrophy, angina, heart failure, stroke, chronic kidney disease, peripheral artery disease 3. Women of child-bearing age who tested positive for HCG & breastfeeding women 4. Individuals who could not read the consent or Participated in another study within 3 months |
Country | Name | City | State |
---|---|---|---|
Pakistan | Riphah Rehabiliation Clinic | Lahore | Punjab |
Lead Sponsor | Collaborator |
---|---|
Riphah International University |
Pakistan,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Blood Pressure | Office, Ambulatory, Daytime, Nighttime & 24 hours Systolic & Diastolic Blood Pressure, Mean Arterial Blood Pressure measured at baseline, 8th Week post treatment and 16th Week post treatment | 16 Weeks | |
Primary | Change in Serum Triglycerides | Serum Triglycerides measured at baseline, 8th Week post treatment and 16th Week post treatment | 16 Weeks | |
Primary | Change in Body Mass Index (BMI) | Body Mass Index (BMI) measured at baseline, 8th Week post treatment and 16th Week post treatment. BMI is calculated using height (m) and weight (kg) using the formula kg/m^2 | 16 Weeks | |
Primary | Change in Forced Vital Capacity (FVC) | Forced Vital Capacity (FVC) measured at baseline, 8th Week post treatment and 16th Week post treatment using a digital spirometer. | 16 Weeks | |
Primary | Change in Serum Total Cholesterol | Serum Total Cholesterol measured at baseline, 8th Week post treatment and 16th Week post treatment from intravenous blood specimen. | 16 Weeks | |
Primary | Change in Serum High Density Lipoprotein (HDL-C) | Serum High Density Lipoprotein (HDL-C) measured at baseline, 8th Week post treatment and 16th Week post treatment from intravenous blood specimen. | 16 Weeks | |
Primary | Change in Serum High Density Lipoprotein (LDL-C) | Serum High Density Lipoprotein (LDL-C) measured at baseline, 8th Week post treatment and 16th Week post treatment from intravenous blood specimen. | 16 Weeks | |
Primary | Change in Forced Expiratory Volume - 01 Second (FEV1) | Forced Expiratory Volume - 01 Second (FEV1) measured at baseline, 8th Week post treatment and 16th Week post treatment using digital spirometer. | 16 Weeks | |
Primary | Change in Forced Expiratory Volume 1 Second / Forced Vital Capacity (FEV1/FVC) | Forced Expiratory Volume 1 Second / Forced Vital Capacity (FEV1/FVC) measured at baseline, 8th Week post treatment and 16th Week post treatment using digital spirometer. | 16 Weeks | |
Primary | Change in Peak Expiratory Flow Rate (PEFR) | Peak Expiratory Flow Rate (PEFR) measured at baseline, 8th Week post treatment and 16th Week post treatment using digital spirometer. | 16 Weeks | |
Primary | Change in Body Fat Percentage | Body Fat Percentage measured at baseline, 8th Week post treatment and 16th Week post treatment using a body fat analyzer | 16 Weeks | |
Primary | Change in Waist-Hip Ratio | Waist-Hip Ratio measured at baseline, 8th Week post treatment and 16th Week post treatment. Waist and hip circumference will be measured using inelastic tape. | 16 Weeks | |
Primary | Change in Hand Grip Strength | Hand Grip Strength (Dominant & Non Dominant)measured at baseline, 8th Week post treatment and 16th Week post treatment using Hand Held Dynamometer. | 16 Weeks | |
Primary | Change in VO2 Maximum | VO2 Maximum measured at baseline, 8th Week post treatment and 16th Week post treatment using treadmill. | 16 Weeks | |
Primary | Change in Level of Perceived Exertion | Level of Perceived Exertion measured at baseline, 8th Week post treatment and 16th Week post treatment using BROG scale. | 16 Weeks |
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