Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03700710
Other study ID # 2018-0433
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 16, 2019
Est. completion date June 30, 2021

Study information

Verified date July 2021
Source Geisinger Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

American College of Cardiology/American Heart Association (ACC/AHA) hypertension guidelines recommend lifestyle modification for patients with elevated blood pressure. While eating a Dietary Approaches to Stop Hypertension (DASH)-type diet, increasing physical activity, and weight loss have been shown to reduce blood pressure, limited resources are available in the primary care setting to help patients make these changes. In this study, the investigators will compare the efficacy of a self-guided vs. dietitian-led approach using web-based lifestyle modification tools to reduce weight, improve dietary quality, and lower blood pressure in overweight/obese adults with elevated blood pressure.


Description:

Goals that all participants will be instructed to target include: 1) weight loss >=3% at 3 months; 2) consume a healthier dietary pattern (high in fruits, vegetables, whole grains, low-fat dairy, vegetable/fish/poultry sources of protein, healthier sources of fat, and avoid sugar and salt); 3) reduce sodium intake to <2300 mg/d; 4) at least 180 min/wk of moderate-intensity physical activity.


Recruitment information / eligibility

Status Completed
Enrollment 187
Est. completion date June 30, 2021
Est. primary completion date June 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 24-hour ambulatory SBP 120-160 mmHg - BMI = 25 kg/m2 - Access to a telephone - Access to a computer or smartphone with internet access - Complete dietary data entry for at least 5 out of 7 days during run-in period - Enter weight into the platform during run-in period Exclusion Criteria: - Inability to understand English - Myocardial infarction, stroke, or atherosclerotic cardiovascular disease procedure within last 6 months. - Current treatment for malignancy - Planned or previous bariatric surgery - Pregnant, breast-feeding, or planned pregnancy prior to the end of participation - Self-reported average consumption of > 21 alcoholic beverages per week or binge drinking. - Psychiatric hospitalization in past year - Current symptoms of angina - Planning to leave the area prior to end of the study - Current participation in another clinical trial - Principal investigator discretion (i.e. concerns about safety, compliance)

Study Design


Intervention

Behavioral:
Self-Guided Approach
For a 12-week period, patients will be asked to access the web platform (Evolve, formerly BMIQ), review educational materials, and enter dietary information. From January 2019 to February 2021, participants used an earlier version of the platform, which was used in tandem with LoseIt (www.loseit.com), a meal-logging app that integrated with the platform. In February 2021, a platform update occurred (Evolve) where the core tenets of the program remained the same and included the dietary data entry directly on the platform.
Dietitian-led Approach
For a 12-week period, patients will be asked to access the web platform (Evolve, formerly BMIQ), review educational materials, and enter dietary information. From January 2019 to February 2021, participants used an earlier version of the platform, which was used in tandem with LoseIt (www.loseit.com), a meal-logging app that integrated with the platform. In February 2021, a platform update occurred (Evolve) where the core tenets of the program remained the same and included the dietary data entry directly on the platform. Dietitians will access the web platform and provided personalized motivational interview phone calls on a weekly basis.

Locations

Country Name City State
United States Geisinger Medical Center Danville Pennsylvania
United States Geisinger Wyoming Valley Wilkes-Barre Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Geisinger Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Change in individual components of Healthy Eating Index score Each individual component of the Healthy Eating Index score will be examined Baseline to 12-week follow-up
Other Satisfaction with the Healthy BP Research Study 5-point Likert score 12-week follow-up
Primary Change in 24-hour Systolic Blood Pressure Measured by 24-hour ambulatory blood pressure monitoring (SpaceLabs Ontrak) Baseline to 12-week follow-up
Secondary Change in 24-hour diastolic blood pressure Measured by 24-hour ambulatory blood pressure monitoring (SpaceLabs Ontrak) Baseline to 12-week follow-up
Secondary Change in Daytime Systolic Blood Pressure Measured by 24-hour ambulatory blood pressure monitoring (SpaceLabs Ontrak) Baseline to 12-week follow-up
Secondary Change in Nighttime Systolic Blood Pressure Measured by 24-hour ambulatory blood pressure monitoring (SpaceLabs Ontrak) Baseline to 12-week follow-up
Secondary Change in Daytime Diastolic Blood Pressure Measured by 24-hour ambulatory blood pressure monitoring (SpaceLabs Ontrak) Baseline to 12-week follow-up
Secondary Change in Nighttime Diastolic Blood Pressure Measured by 24-hour ambulatory blood pressure monitoring (SpaceLabs Ontrak) Baseline to 12-week follow-up
Secondary Change in Total Healthy Eating Index - 2015 score Assessed by Viocare Food Frequency Questionnaire (score 0-100, 100=best possible score) Baseline to 12-week follow-up
Secondary Change in Weight Weight measured at baseline and 12-week visits without shoes Baseline to 12-week follow-up
Secondary Change in Waist Circumference Measured using a tape measure Baseline to 12-week follow-up
Secondary Change in Physical Activity (metabolic equivalent of task [MET]-minute per week Measured by International Physical Activity Questionnaire (IPAQ) Short Form Baseline to 12-week follow-up
See also
  Status Clinical Trial Phase
Not yet recruiting NCT03994419 - PErioperAtive CHildhood ObesitY
Recruiting NCT05354245 - Using a Complex Carbohydrate Mixture to Steer Fermentation and Improve Metabolism in Adults With Overweight and Prediabetes (DISTAL) N/A
Completed NCT03602001 - Attentive Eating for Weight Loss N/A
Recruiting NCT06269159 - The Power of 24-hour: Co-designing Intervention Components
Completed NCT03377244 - Healthy Body Healthy Souls in the Marshallese Population N/A
Completed NCT02996864 - Location-based Smartphone Technology to Guide College Students Healthy Choices Ph II N/A
Terminated NCT03914066 - A Group-based Treatment of Overweight and Obesity in Primary Care N/A
Completed NCT04647149 - Effects of Early and Delayed Time-restricted Eating in Adults With Overweight and Obesity N/A
Completed NCT03685656 - Effect of ANACA3 Slimming Gel on Loss of Abdominal and Thigh Circumferences in Healthy Volunteers N/A
Completed NCT05051579 - A Study of LY3502970 in Participants With Obesity or Overweight With Weight-related Comorbidities Phase 2
Completed NCT04611477 - Effect of Synbiotic 365 on Body Composition in Overweight and Obese Individuals N/A
Active, not recruiting NCT05330247 - Cut Down on Carbohydrate in the Dietary Therapy of Type 2 Diabetes - The Meal Box Study N/A
Completed NCT03599115 - Effects of Inhibitory Control Training in Eating Behaviors N/A
Recruiting NCT05938894 - Train Your Brain - Executive Function N/A
Recruiting NCT06094231 - Treating Patients With Renal Impairment and Altered Glucose MetAbolism With TherapeutIc Carbohydrate Restriction and Sglt2-Inhibiton - a Pilot Study N/A
Recruiting NCT05987306 - A Self-compassion Focused Intervention for Internalized Weight Bias and Weight Loss N/A
Completed NCT03792685 - Looking for Personalized Nutrition for Obesity/Type 2 Diabetes Mellitus Prevention N/A
Completed NCT05055362 - Effect a Honey, Spice-blended Baked Good Has on Salivary Inflammation Markers in Adults: a Pilot Study N/A
Completed NCT04520256 - Rapid Evaluation of Innovative Intervention Components to Maximize the Health Benefits of Behavioral Obesity Treatment Delivered Online: An Application of Multiphase Optimization Strategy Phase 2/Phase 3
Completed NCT04979234 - A Single Centre, Prospective Feasibility Study to Evaluate the Efficacy of an Endoluminal-suturing Device (Endomina) on Severe Obstructive Sleep Apnea Syndrome N/A