Evaluation of a Commercial Program on Weight Loss and Health Outcomes

NCT ID: NCT02585193

Last Updated: 2017-08-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 150 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-08-31
• Study Completion Date: 2016-03-31

Brief Summary

While some evidence on weight change elicited from commercially available weight loss programs, such as Weight Watchers, is available, there is little evidence evaluating any health-related outcomes that result from losing weight through these programs. In addition, little data exists on the adherence and satisfaction of these types of programs. The purpose of this study is to evaluate body weight and health-related outcomes that are achieved from participating in a Weight Watchers program, along with program adherence and satisfaction. Men and women (N=150) that are participating in Weight Watchers weight loss program will undergo assessments at the University of Pittsburgh to evaluate outcomes related to the Weight Watchers 6 month intervention. Assessment visits, separate from the intervention, will take place at baseline (0 months), 3 months and 6 months for approximately 90 minutes at the Physical Activity and Weight Management Research Center. Participants will be asked to undergo assessments of body weight, height, aerobic stamina, functional fitness, flexibility, and complete a series of questionnaires related to demographics, program satisfaction, sleep quality, happiness, and food cravings. Adherence to the program will be measured by the number of group sessions attended.

Detailed Description

There is a body of evidence that has evaluated the effect of Weight Watchers, a commercially available weight loss program, on changes in body weight. The current investigation aims to add to this body of evidence by providing additional data on changes in body weight and enhance the current evidence-base in regards to evaluating other health-related outcomes.

There is no evidence that demonstrates whether or not the weight loss as a result of the Weight Watchers program elicits changes in health-related outcomes related to aerobic capacity, flexibility, functional fitness, sleep, and other psychological measures. Additionally, within a scientific research protocol, measures of adherence and satisfaction have not been evaluated. This study will evaluate these outcomes beyond weight changes achieved across the 24-week program.

Conditions

Weight Loss

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Weight Watchers Intervention

All participants are enrolled in this single arm of the study. All participants receive the Weight Watchers intervention which consists of weekly group intervention/support meetings in which weight loss behaviors (diet, physical activity) are discussed.

Group Type: OTHER

Weight Watchers Intervention

Intervention Type: BEHAVIORAL

All participants are enrolled in this single arm of the study. All participants receive the Weight Watchers intervention which consists of weekly group intervention/support meetings in which weight loss behaviors (diet, physical activity) are discussed.

Interventions

Weight Watchers Intervention

All participants are enrolled in this single arm of the study. All participants receive the Weight Watchers intervention which consists of weekly group intervention/support meetings in which weight loss behaviors (diet, physical activity) are discussed.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Male or female over age 18. Set "soft quotas" on the number of male and female participants - The desire is to have a 90% female / 10% male split.
• With or without previous Weight Watchers experience. Set quota on the number of participants with previous Weight Watchers experience at 65%.
• Self reported height/weight resulting in a Body Mass Index (BMI) of 27 to 43 kg/m2 (will re-screen at facility).
• Self report that he/she feels the need to lose weight.
• Willing to discontinue any current over-the-counter (OTC) supplements not recommended/prescribed by physician, with the exception of multivitamins or other vitamin supplement.
• Willing to follow recommendations required by study protocol.
• Willing to include demographic information (e.g., ethnicity, income and education).
• Willing to participate in consumer surveys and focus groups as a part of the intervention.
• Use of a personal smartphone on a daily basis. For Android devices, must be version 4.4 (code: KitKat) or 5.0 (codename: Lollipop). For iPhones, must be iOS6 and above. Cannot accommodate Blackberry devices.
• The willingness and ability to navigate and use applications on their smartphone on a daily basis (minimum training will be provided).
• Reliable home WiFi access
• Ability to commit to attending up to 27 study visits in approximately 26 weeks:

• Ability to commit (to best of their ability) to attending weekly meetings, 30-60 minutes in duration, at the same day and time each week for 24 consecutive weeks (daytime and evening options will be available).
• Ability to commit to up to 3 additional study visits at Weeks 0, 12, and 24, each approximately 90 minutes in duration, to complete assessments (height, weight, questionnaires, physical measures).

Exclusion Criteria

• Participants that are currently following a commercial weight-loss program.
• Participants that have been involved in a related market research program within the last 6 months.
• Pregnant or nursing, or planning on becoming pregnant over the next 9 months.
• Recent weight loss of ≥ 5 kg in the previous 3 months.
• History of clinically diagnosed eating disorder.
• Orthopedic limitations preventing participation in regular physical activity.
• Untreated thyroid disease or > 1 change in dose or type of thyroid medication over previous 6 months.
• Taking any prescription medication with known effects on appetite or weight.

*With the exception of subjects on a stable dose of SSRIs (Selective Serotonin Re-uptake Inhibitors) for 6 months.

• Taking oral steroids.
• Chronic/inflammatory gastrointestinal disorders (irritable bowel syndrome acceptable).
• Previous surgical procedure for weight loss.
• Major surgery within the previous 3 months.
• History of heart problems (e.g., angina, bypass surgery, MI, etc) within previous 3 months.
• Presence of implanted cardiac defibrillator or pacemaker.
• Uncontrolled hypertension self-reported BP > 160/100mmHg)
• Diuretic use for hypertension over 1.5mg per day
• Diagnosis of type 1 or type 2 diabetes
• History of presence of cancer (completely respected basal or squamous cell carcinoma acceptable if treatment completed more than 6 months prior to enrollment).
• Consuming more than 14 alcoholic drinks per week or not more than 3 drinks per day.
• Planning to relocate in the next 9 months
• Any orthopedic limitation preventing participation in regular physical activity.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Pittsburgh

OTHER

Sponsor Role: lead

Responsible Party

Renee J. Rogers

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Renee J Rogers, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

Locations

Physical Activity and Weight Management Research Center / University of Pittsburgh

Pittsburgh, Pennsylvania, United States

Countries

United States

Other Identifiers

PRO15040047

Identifier Type: -

Identifier Source: org_study_id