Weight Loss Maintenance (WLM) (WLM)
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|ClinicalTrials.gov Identifier: NCT00054925|
Recruitment Status : Completed
First Posted : February 14, 2003
Last Update Posted : March 7, 2012
|Condition or disease||Intervention/treatment||Phase|
|Cardiovascular Diseases Heart Diseases Obesity Diabetes Mellitus, Non-insulin Dependent Hypertension||Behavioral: Personal contact (PC) Behavioral: Interactive technology (IT)||Not Applicable|
Overweight/obesity is the second leading cause of death in the US, and is growing in prevalence at an alarming rate. Control of overweight/obesity is increasingly recognized as a high national priority because of its contribution to cardiovascular (CVD) risk factors and ultimately to CVD itself. The short-term success of behavioral interventions for weight loss has been repeatedly documented. Unfortunately, because weight re-gain is extremely common, a disappointingly, small proportion of individuals achieve long-term weight control. Of the factors that are associated with sustained weight loss, one of the most important is continued intervention with frequent contacts.
The study is a multi-center, randomized, controlled trial [Weight Loss Maintenance Trial (MAINTENANCE)] to determine the effects of two innovative behavioral interventions, each designed to maintain frequent contacts, compared to a usual care control group. Overweight and obese individuals (60% women, 40% African Americans) who are taking medication for hypertension, dyslipidemia and/or type 2 diabetes will enter a 6-month, weight loss program. Those 800 individuals who lose at least 4 kg (approximately 9 pounds) will then be randomized into one of three groups: a Personal Contact (PC) Intervention that provides monthly personal contacts with a trained interventionist, primarily via telephone; an Interactive Technology (IT) Intervention that provides frequent contacts through a state-of-the-art interactive web-based program supplemented by other communication technologies; or Usual Care (UC). The primary outcome will be weight change from the end of the initial weight loss program to the end of the 30-month weight maintenance intervention period. Other outcomes will include weight change in subgroups, prevalence of CVD risk factors, measures of behavior change, and cost of implementation. For each outcome, the Personal Contact and Interactive Technology interventions will be compared to Usual Care and, if different from Usual Care, to each other. To successfully combat the obesity epidemic, clinicians and health care systems must have options that are effective and feasible and that can be provided to large numbers of individuals.
Phase II intervention completed: July 2007
Phase III intervention completed: October 2009
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||1685 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||Weight Loss Maintenance (WLM)|
|Study Start Date :||January 2003|
|Actual Primary Completion Date :||October 2009|
|Actual Study Completion Date :||October 2009|
Active Comparator: Personal contact (PC)
The Personal Contact (PC) intervention offers one-on-one guidance and support in maintaining weight loss.
Behavioral: Personal contact (PC)
This arm uses brief, individual contacts on a monthly basis which emphasize core elements of weight maintenance. Monthly contacts with an interventionist occur for 30 months after the end of Phase I. Face-to-face contacts occur approximately every four months (e.g., three annually), with telephone contacts occurring every month between FTF contacts.
Active Comparator: Interactive technology (IT)
Utilizes internet and automated phone technology to enhance the frequency and timeliness of feedback.
Behavioral: Interactive technology (IT)
The website utilizes collaborative goal setting and problem-solving strategies to identify contingent action plans for perceived obstacles to success. In order to tailor the intervention to the needs of the participant, the action plan can be updated anytime and as frequently as desired by the individual. Participants are encouraged to input data on weight, food records, physical activity, and goals on a weekly basis. Participants are not restricted to logging on to the website only once a week. Rather, participants have the option of logging on to the website to enter data, communicate with other participants, or to seek other information, as frequently as they wish.
- Change in Weight [ Time Frame: Baseline to 30 months ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00054925
|Principal Investigator:||Lawrence Appel||Johns Hopkins University|
|Principal Investigator:||Phillip Brantley||LSU Pennington Biomedical Research Center|
|Principal Investigator:||Jack Hollis||Kaiser Foundation Research Institute|
|Principal Investigator:||Victor Stevens||Kaiser Foundation Research Institute|
|Study Chair:||Laura Svetkey||Duke University|