- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00948415
Evaluation of the Shape Up Rhode Island Campaign Study 5
Evaluation of the Shape Up Rhode Island Campaign Study 5: Does Adding Behavioral Weight Control Information to Shape-Up Rhode Island Improve Outcomes?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Background: Given the epidemic of obesity, approaches to weight loss that can be applied on a community, state, or national level are needed. This project is an ongoing evaluation of Shape Up Rhode Island (SURI) program, a state-wide Internet based program involving team-based competition to increase physical activity and achieve weight loss.
Aim: To enhance the effectiveness of SURI utilizing a minimal contact intervention delivered online.
Design: SURI 2009 participants were invited to join a research study focusing on weight loss. Interested participants were randomized to two groups including a SURI Enhanced group (behavioral intervention presented in 12 weekly online presentations, daily self-monitoring, and weekly automated feedback) or a SURI Standard group (group given a list of previously existing online resources to aid with weight loss).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Rhode Island
-
Providence, Rhode Island, United States, 02903
- The Miriam Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Overweight or obese
- Current participant in the Shape Up RI program weight loss competition
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: SURI Enhanced
|
The SURI enhanced group will receive the standard Shape Up RI program.
In addition, participants will be asked to record and report their daily calorie intake, body weight, minutes of physical activity, and pedometer steps.
Participants will receive automated feedback on progress as well as a behavioral lesson delivered online during each week of the program.
Participants assigned to the SURI Standard arm will receive the standard Shape Up RI program.
The intervention will take place during the 12-week Shape Up RI campaign.
|
Active Comparator: SURI Standard
|
The SURI enhanced group will receive the standard Shape Up RI program.
In addition, participants will be asked to record and report their daily calorie intake, body weight, minutes of physical activity, and pedometer steps.
Participants will receive automated feedback on progress as well as a behavioral lesson delivered online during each week of the program.
Participants assigned to the SURI Standard arm will receive the standard Shape Up RI program.
The intervention will take place during the 12-week Shape Up RI campaign.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Weight loss at the end of Shape Up RI
Time Frame: 3 Months
|
3 Months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Weight loss maintenance 6 months after program completion
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2097-07 Study 5
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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