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Remote Delivery of Weight Management by Phone and Social Media

Remote Delivery of Weight Management by Phone and Social Media

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02496871
Enrollment
70
Registered
2015-07-14
Start date
2015-07-31
Completion date
2020-02-25
Last updated
2020-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Brief summary

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

Detailed description

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.

Interventions

University of Kansas Weight Management Program - Group Phone calls

BEHAVIORALSocial Media

University of Kansas Weight Management Program - Social Media (Facebook)

Sponsors

Blue Cross Blue Shield
CollaboratorOTHER
Kansas City Area Life Sciences Institute, Inc.
CollaboratorOTHER
University of Kansas Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Change in weightChange from Baseline to Month 6

Secondary

MeasureTime frameDescription
Change in BMIChange from Baseline to Month 6
Physical activity - stepsMonth 6Measured using pedometer to report steps per day on a weekly basis
Physical activity - total minutesMonth 6Average of total minutes per week of physical activity
Physical activity - ActiGraph Activity Level (Count/Minute; CPM)7 daysAverage ActiGraph counts/minute over 7-day period. Activity level based on cut points used in NHANES as described by Troiano. Cut points used will be Sedentary: 0 - 99 CPM; Light: 100 - 2019 CPM; Moderate: 2020 - 5998 CPM; Vigorous: 5999 - ∞ CPM.
Quality of Life Assessment (SF-36)Change from Baseline to Month 6Measured using the Short Form 36 (SF-12) Health Survey.
Quality of Life - Weight RelatedChange from Baseline to Month 6Measured using the SHIELD-WQ-9 Questionnaire
Feasibility of Interventions - adherence to protocol proceduresMonth 6Participants adherence to diet, physical activity and attendance/participation in weight loss sessions.
Dietary assessment - self-reported logMonth 6Participants will complete dietary intake log, including 2 weekdays and 1 weekend day, using MyFitnessPal application prior to baseline and month 6 visits.

Other

MeasureTime frame
Cost Analysis of InterventionsMonth 6

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026