NCT Number: NCT03532815
Lifestyle Intervention for Cardiovascular Disease Risk Factors Among Female Residents at the National Guard Residential City, Jeddah, Saudi Arabia
Cardiovascular disease (CVD) remains the major cause of mortality globally. Applying a comprehensive interventional program based on the individual's risk may reduce the incidence and complications of CVD; thus, helping to decrease the burden on the healthcare system. This study compared the effects of a 3-month intervention involving lifestyle modification and physical activity with standard care in women ≥30 years having a moderate-to-high risk of CVD, with respect to improving physical activity and cardiovascular disease risk factors at the National Guard Residential City in Jeddah, Saudi Arabia, in 2015. The effects of this community-based lifestyle program were assessed through a randomized controlled trial. Women in the intervention group (n=31) received health education, exercise training, and diet counselling as individuals and in groups according to the participant's risk. Women in the control group (n=28) received one health education session at the screening site. The Framingham risk score (FRS) was calculated at baseline and at 3 months for both groups. The mean participant age was 42±8 years.
Looking for future studies?
Notify MeKey information
Conditions
Age range
30 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Women aged ≥ 30 years.
- The participants must be at moderate to high-risk of CVD according to FRS.
Exclusion criteria
- Women aged < 30 years.
- Women aged ≥ 30 years with low risk of CVD according to FRS.
- Pregnant women.
- Female patients diagnosed with CVD.
Treatment and study plan
Primary outcomes
-
Framingham Risk Scores Reduction
Time frame: 3 months
The proportion of individuals with moderate Framingham risk scores (FRS) reducing their risk by 10% and the proportion of individuals with high (FRS) reducing their risk by 25% using the Framingham risk score. It consists of six point scores including age, total cholesterol, smoking status, HDL level, diabetes status, systolic Blood Pressure and Treatment Status. The sum of these points will result in an estimate of the 10-Year risk of developing cardiovascular event and for risk categorization of low (< 10% FRS), moderate (10%-19% FRS), or high risk (≥ 20% FRS).
Secondary outcomes
-
Framingham Risk Category Changes
Time frame: 3 months
The proportion of individuals reducing their risk by ≥ 1 risk category using the Framingham risk score. It consists of six point scores including age, total cholesterol, smoking status, HDL level, diabetes status, systolic Blood Pressure and Treatment Status. The sum of these points will result in an estimate of the 10-Year risk of developing cardiovascular event and for risk categorization of low (< 10% FRS), moderate (10%-19% FRS), or high risk (≥ 20% FRS). .
Sponsors and collaborators
Lead sponsor
King Abdullah International Medical Research Center
Other
Registry information
Official study title
A Randomized Controlled Trial of Lifestyle Intervention for Cardiovascular Disease Risk Factors Among Female Residents at the National Guard Residential City, Jeddah, Saudi Arabia, 2015
Important dates
- Study start
- 2015
- Primary completion
- 2015
- Study completion
- 2015
- First posted
- May 22, 2018
- Registry last updated
- Nov 6, 2019
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Related clinical trials
Published trials that share one or more normalized conditions with this study.
Web-based Physical Activity Intervention to Promote Physical Activity
NCT05803304
Behavior, Cardiovascular Diseases
Atlanta, Georgia, United States
View Trial DetailsSYMPHONY-PE Study for Treatment of Pulmonary Embolism
NCT06062329
Acute Pulmonary Embolism, Cardiovascular Diseases
Huntsville, Alabama, United States
View Trial DetailsAB-1002 in Patients With Class III Heart Failure
NCT04179643
Arrhythmias, Cardiac, Cardiovascular Diseases
Minneapolis, Minnesota, United States
View Trial DetailsDietary Nitrate and Nitrite Intake and Phosphate Biomarkers and Risk of Chronic Diseases
NCT07746310
Asthma, Asthma (Diagnosis)
Stockholm, Sweden
View Trial Details