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BMI clinical trials

View clinical trials related to BMI.

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NCT ID: NCT05383456 Completed - HIV Clinical Trials

The Visceral Adiposity Measurement and Observation Study

VAMOS
Start date: April 18, 2022
Phase:
Study type: Observational

The Visceral Adiposity Measurement and Observation Study

NCT ID: NCT05030844 Completed - Type2 Diabetes Clinical Trials

The Effect of IMB Model-Based Diabetes Education and Motivational Interviewing on Care Outcomes in Adults With T2DM

Start date: July 14, 2021
Phase: N/A
Study type: Interventional

This study was conducted to examine the effects of IMB model-based diabetes education and Motivational Interviewing for adults with Type 2 diabetes on care outcomes This study was conducted to examine the effects of IMB model-based diabetes education and Motivational Interviewing interventions on care outcomes for adults with Type 2 diabetes (diabetes knowledge, health belief, self-efficacy, self-management, HbA1c and BKÄ°).

NCT ID: NCT04371614 Completed - Stress Clinical Trials

PTSC: Improving Hypertension Control Among Poor Midlife African American Women

PTSC-RCT
Start date: July 14, 2016
Phase: N/A
Study type: Interventional

African American women are more likely to suffer higher rates of uncontrolled hypertension than non-Hispanic white women. Prime Time Sister Circles® (PTSC) empowers women to proactively manage their blood pressure by promoting the effective use of preventive health care; encouraging self monitoring of blood pressure, and teaching strategies for managing stress, increasing physical activity, and improving nutrition. The 12-week community-based, holistic lifestyle intervention aims to improve blood pressure control by improving health knowledge, health efficacy, and health behaviors. PTSC potentially reduces health care costs through prevention, earlier detection, and improved management of hypertension through a culturally tailored program addressing specific barriers experienced by midlife and late life African American women. This 5-year study is a collaboration between The Johns Hopkins Center for Health Disparities Solutions (HCHDS), The Gaston & Porter Health Improvement Center, Inc. (GPHIC), and the American Institutes for Research (AIR). The investigators seek to determine the impact and cost-effectiveness of the PTSC intervention among low-income African American women with uncontrolled hypertension. To do this, the investigators will randomly assign 600 women between the ages of 40 and 75 who receive their care from an federally qualified health center (FQHC) to either PTSC (n=300) or a comparison group (n=300) who will receive the PTSC intervention after they have been observed for 15 month. Using data from in person surveys and clinical measures conducted during in-person data collection meetings, the investigative team will determine if PTSC help low-income African American women effectively manage their blood pressure.

NCT ID: NCT03519620 Completed - Child Development Clinical Trials

Swimming and Water Walking on Spirometry Values

ESWWSV
Start date: March 3, 2018
Phase: N/A
Study type: Interventional

To study the effects of swimming with water walking in children aged between 6 and 12 years in terms of spirometric values.

NCT ID: NCT03251950 Completed - Blood Pressure Clinical Trials

Food Resource Equity and Sustainability for Health

FRESH
Start date: August 22, 2017
Phase: N/A
Study type: Interventional

Food insecurity increases the risk of obesity, diabetes, hypertension, and cancer. American Indians (AIs) in Oklahoma are three times as likely as Whites to be food-insecure (21% vs. 7%) and have burdens of obesity (42%), hypertension (38%), and diabetes (15%) that exceed those of the general US population. While individual-level obesity prevention efforts have been implemented with AIs, few environmental interventions to reduce food insecurity and improve fruit and vegetable intake have been conducted with tribal communities. Community gardening interventions have been shown to increase vegetable and fruit intake, reduce food insecurity, and lower BMI among children and adults; however, to date, no such interventions have been evaluated with AI families. The proposed study, entitled "Food Equity Resource and Sustainability for Health (FRESH)," will assess the impact of a tribally-initiated community gardening intervention on vegetable and fruit intake, food insecurity, BMI, and blood pressure in families living on the Osage Nation reservation in Oklahoma.

NCT ID: NCT02947659 Completed - Clinical trials for BMI, Academic Stress and MSDs Relationships

Body Mass Index, Academic Stress and Musculoskeletal Disorders Relationships

Start date: October 2015
Phase: N/A
Study type: Observational

[Purpose] To investigate the prevalence of musculoskeletal disorders among healthy students of Ahlia University and to determine the relationship between the prevalence of musculoskeletal disorders and academic stressors and body mass index. [Subjects and Methods]: Self-administered questionnaires were distributed to 94 students aged 18-26 years who were enrolled at various Ahlia University colleges and met other inclusion criteria. The students responded to the standardized Nordic musculoskeletal questionnaire and the modified College Student Stress Inventory regarding musculoskeletal symptoms and academic stressors. Height and weight measurements were also obtained to determine body mass index. Keywords: Body mass index, Academic stress, Musculoskeletal disorders

NCT ID: NCT01886495 Completed - Tangier Disease Clinical Trials

Effect of High Protein Diet on Adiponectin and Inflammation Among Overweight and Obese Children

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The investigators aimed to determine the effects of HP diet on adiponectin and inflammatory factors among overweight and obese children.

NCT ID: NCT01886482 Completed - Tangier Disease Clinical Trials

Effect of High Protein Diet on Cardiovascular Diseases Risk Factors Among Overweight and Obese Children

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The investigators aimed to determine the effects of HP diet on CVD risk factors among overweight and obese children.

NCT ID: NCT01763528 Completed - Tangier Disease Clinical Trials

High Protein Weight Loss Diet, High Sensitivity C-Reactive Protein and Cardiovascular Risks Among Obese Women

Start date: January 2011
Phase: Phase 3
Study type: Interventional

The investigators aimed to determine the effects of HP diet on CVD risk factors and hs-CRP among overweight and obese women.

NCT ID: NCT01143571 Completed - BMI Clinical Trials

Evaluation of Skin, Colonic, and Oral Microbiome and Effect of Time and Antibiotic Treatment on Organism Diversity at Each Site

Start date: November 20, 2009
Phase:
Study type: Observational

Background: - Most studies of infectious agents have focused on specific microbes, such as human papillomaviruses and cervical cancer, and the hepatitis B and C virus and liver cancer. The skin and many internal areas (including the mouth and the gastrointestinal tract) also contain large numbers of naturally occurring microbes, but these areas have not received as much study. - Some of the infectious agents that naturally reside in the body may have an effect on health. The study of naturally occurring microbes in the human body is a new area of research, and much remains to be learned regarding the extent and pattern of their appearance and appropriate techniques for testing them. - Researchers are interested in collecting human samples from areas known to contain naturally occurring microbes. These samples will provide baseline information for further studies. Objectives: - To collect a set of study samples from individuals who have applied to participate in a study assessing the relationship among the bacteria H. pylori, peptic ulcer disease, and gastric cancer. Eligibility: - Individuals between the ages of 21 and 65 who are participating in the clinical trial entitled A Phase III Randomized Trial of Three Antibiotic Regimens to Eradicate Helicobacter Pylori. Design: - Researchers will collect oral (saliva), colonic, and skin swab samples from study participants who tested positive for the presence of the H. pylori bacteria. These samples will be collected at the three study visits (enrollment, 6 weeks, and 1 year). - Researchers will also collect samples from people who applied for the clinical trial but did not test positive for H. pylori. These samples will be collected at the enrollment visit and 1 year later. - Blood samples will be collected at each study visit.