LIVE SMART: Smartphone Intervention for Weight Control
Completed · Not applicable
Conditions studied: Overweight, Obesity
In brief
The purpose of this study is to compare three methods of delivering behavioral weight loss treatment.Participants are randomly assigned to one of three 18-month weight loss treatments (group, individual, or smartphone treatment). Participants who are assigned to group treatment will attend group meetings weekly for the first 6 months, then every 2 weeks for 6 months, and then monthly for the final 6 months. Participants who are assigned to individual treatment will attend one-on-one sessions with a weight loss counselor every month for 18 months. Participants who are assigned to smartphone treatment will use a smartphone to learn and practice weight loss skills. They will also attend one-on-one sessions with a weight loss counselor every month for 18 months. Assessment visits are conducted at baseline, 6, 12, and 18 months.
Key facts
- Study ID
- NCT01724632
- Run by
- The Miriam Hospital
- People needed
- 276
- Starts
- 2012-11-01
- Expected to finish
- 2016-08-01
- Last updated by the study team
- 2017-05-30
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Body Mass Index (kg/m2) of 25-45.
- English language fluency
- Ability to read at a 6th grade level
- Availability to attend weekly treatment sessions in Providence, RI
You may not qualify if…
- Any heart condition that limits ability to participate in physical activity
- Chest Pain
- Any cognitive of physical limitation that would preclude use of a smartphone
- Serious mental illness
- Historical or current eating disorder
- Previous or planned bariatric surgery
- Use of weight loss medication
- Recent pregnancy or a plan to become pregnant in the next 6 months
- Participation in a study at the Weight Control and Diabetes Research Center within the last two years
- A weight loss of greater than 5% body weight in the last 6 months
Where it is running
- Weight Control and Diabetes Resarch Center — Providence, Rhode Island, United States
Full record on ClinicalTrials.gov
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