Obesity Clinical Trial
Official title:
A Comparison of Video Conferencing and In-person Health Coaching Approaches in Combination With mHealth Devices on Weight Loss, Physical Activity, and Glycemic Control
Verified date | September 2017 |
Source | University of New Mexico |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study was to determine how 12 weeks of health coaching with individualized feedback and education in combination with mobile health devices (a digital wireless body weight scale and wireless activity tracker) influences body weight, waist circumference, physical activity levels, and select blood-borne markers of health (fasting blood glucose, hemoglobin A1c, and insulin). The individualized health coaching, education, and feedback was delivered by either video conferencing or direct, in-person consultation. All education materials including (i.e. video modules, exercise manuals, nutrition manuals) were designed and compiled by a team of health professionals from (inHealth Medical Services, Inc.). These materials focused on incorporating behavioral principles of self-monitoring, exercise, nutrition, goal setting, and behavior modification. Each participant was randomly assigned into one of two intervention groups (a video conferencing or in-person group) or a control group.
Status | Completed |
Enrollment | 30 |
Est. completion date | May 30, 2017 |
Est. primary completion date | May 20, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: Fluent in English spoken and written at a high-school level, Non-diabetic Obese according to body mass index (BMI) standards (> 30 kg/m2), Weigh less than 396 pounds, Live a sedentary lifestyle defined as < 7,000 steps per day Had access to an Apple® iPhone or Android® smart phone Exclusion Criteria: - Participants were excluded if they have stated having an Immunodeficiency disorder Kidney disease; Type II diabetes; History of uncontrolled high blood pressure (defined as a systolic blood pressure = 140mmHg and/or diastolic blood pressure =90 mmHg confirmed by measurements on two separate occasions); Asthma, COPD, Heart attack or stroke within the past 12 months; Presence of a partial or full artificial limb; Known dementia, brain cancer, eating disorders, history of significant neurological or psychiatric disorder or any other psychological condition; Medications, dietary supplements, or substances advertised to modify metabolism or body weight; Undergone major surgery less than 4 weeks prior to enrollment in the study; or were actively losing weight. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of New Mexico | inHealth Medical Services, Inc., National Institute of General Medical Sciences (NIGMS) |
American Heart Association; American College of Cardiology; Obesity Society. Reprint: 2013 AHA/ACC/TOS Guideline for the Management of Overweight and Obesity in Adults. J Am Pharm Assoc (2003). 2014 Jan-Feb;54(1):e3. doi: 10.1331/JAPhA.2014.14502. Review. — View Citation
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Weight loss in (kg) | Investigators examined body weight changes between groups baseline (week 0) and post intervention (week12). | Change in weight between baseline (week 0) and post intervention (week 12) | |
Secondary | Comparison of daily step average per day by group (n=10 for each group). | Investigators examined steps per day and averaged them every week. Each time point (weeks) were then graphed and presented as adjusted least mean square (LMS) and standard error (SE). | Average steps per day/week over a 12 week period. | |
Secondary | Hba1c pre and post intervention | Investigators measured HbA1c via a blood test which was analyzed by Quest® laboratories. | Pre and Post (a 12 week study) | |
Secondary | Insulin pre and post intervention | Investigators measured Insulin via a blood test which was analyzed by Quest® laboratories. | Pre and Post (a 12 week study) | |
Secondary | Blood glucose pre and post intervention | Investigators measured blood glucose via a blood test which was analyzed by Quest® laboratories. | Pre and Post (a 12 week study) | |
Secondary | Homeostasis Model Assessment Insulin resistance (HOMA-IR) | A Homeostasis Model Assessment was used to estimate insulin resistance (HOMA-IR) | Pre and Post (a 12 week study) |
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