Expired Study
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Springfield, Oregon 97477


Purpose:

This is a six month lifestyle management study to compare the effects of iWell; a dynamic online interactive technology to a self-directed program in overweight or obese individuals. The primary aim is to test the hypothesis that dynamic online interactive technology intervention is more effective than self-directed program in obtaining and maintaining weight loss and other biometric improvements.


Study summary:

Optimal health behavior is difficult to sustain over extended periods. This study seeks to demonstrate that technology can be a low cost scaleable solution that will provide the user with sufficient customization and personalization through social networking approaches such that sustainability of optimal health behavior is realized.


Criteria:

Inclusion Criteria: - age 18-70 years old - overweight or obese men and women with BMI between 24 and 38, inclusive - concerned about weight/health (and motivated in losing weight) - stable medications for past 3 months - willing/able to use Web-based services - willingness not to use weight loss medications for the duration of the trial - able and willing to give informed consent and participate in the interventions - willing to come to three sessions and visits - willingness to be randomized to intervention or control group Exclusion Criteria: - contraindication to weight loss (e.g., malignancy or other serious illness) - Type 1 DM and Type 2 DM with other end organ compromise (renal, retinal or other) - Recent (within 6 months) cardiovascular event (MI or stroke) - current symptoms of angina - heart, renal, or liver disease (excluding kidney stone) - cancer or active neoplasm (excluding skin cancers) - hyperthyroidism - mental conditions that would preclude full participation - prior weight-loss (bariatric) surgery or plan for these procedures - liposuction surgery in past 12 months or plan for these procedures - recent weight loss in the past 3 months (>20 lbs) - use of prescription weight loss medication in 3 months prior to screening - current use of medications for treatment of psychosis or manic-depressive illness


NCT ID:

NCT01325376


Primary Contact:

Principal Investigator
Brigitte Piniewski, MD
PeaceHealth Laboratories


Backup Contact:

N/A


Location Contact:

Springfield, Oregon 97477
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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