Remote Delivery of Weight Management by Phone and Social Media



Status:Active, not recruiting
Conditions:Obesity Weight Loss
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:21 - 70
Updated:3/8/2019
Start Date:July 2015
End Date:July 31, 2020

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The purpose of this study is to compare two different weight management delivery methods,
social media versus a traditional care model.

Obesity is a major public health issue as 68% of the US population is either overweight or
obese. Weight loss and weight loss maintenance is difficult. Traditionally, successful weight
loss programs are weekly behaviorally-based clinics which utilize a combination of calorie
restriction and physical activity. Traditional "face to face" weekly meetings may not be
feasible for everyone.

An alternative to provide weight loss and weight maintenance created by KUMC researchers uses
weekly group phone conference calls. While this method produced equal weight loss with fewer
burdens to participants when compared to the traditional "face to face" format, weight regain
during maintenance was still high.

This study will investigate a new delivery method (social media platform "Facebook") compared
to the group phone conference calls. In the social media platform participants will be able
to socialize with other participants in their group by commenting on posts from other
participants or posting messages themselves. Social media delivered programs have potential
to be a more a cost-effective approach to reach a large group of individuals.

Participants who are eligible and decided to be in this study will take part in study related
activities for 6 months.

Inclusion Criteria:

- Body mass index (BMI) of 30 to 45 kg/m^2

- Have access to a computer, smart phone, or tablet

- Give informed consent to participate

Exclusion Criteria:

- Unable to participate in moderate intensity PA (i.e., walking)

- Participation in a weight loss or physical activity program in the previous 6 mos.

- Greater than 3, 30-min bouts of planned exercise/week

- Not weight stable (±4.6 kg) for 3 mos. prior to intake

- Unwilling to be randomized to 1 of the 2 study groups

- Report being pregnant during the previous 6 mos., currently lactating, or planned
pregnancy in the following 6 mos.

- Serious medical risk such as cancer, recent cardiac event (i.e. heart attack, stroke,
angioplasty) as determined by the individual's PCP via the clearance to participate in
the investigation

- Current use of antipsychotics or untreated depression

- Adherence to specialized diet regimens, i.e., multiple food allergies, vegetarian,
macrobiotic

- Binge eating disorder as assessed by the Binge Eating Scale

- Living in the same household as another study participant
We found this trial at
1
site
3901 Rainbow Blvd
Kansas City, Kansas 66160
(913) 588-5000
University of Kansas Medical Center The University of Kansas Medical Center serves Kansas through excellence...
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