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Evaluation of a Commercial Program on Weight Loss and Health Outcomes

Primary Purpose

Overweight and Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Modified Weight Watchers plan
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overweight and Obesity

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Body mass index (BMI) between 25 and 43 kg/m²
  • Ability to read and speak English
  • All ethnic groups will be recruited
  • Self-report desire to lose weight and willing to follow study recommendations
  • Use of an iPhone with iOS 8.0 or later for use on a daily basis, and basic app skills
  • Have access to the internet via a computer, and basic computer skills

Exclusion Criteria:

  • Currently following a commercial weight-loss program (including Weight Watchers) or who followed a weight loss program in the previous 6 months or who were members of Weight Watchers within the past 12 months
  • Another member of the household participating in the study.
  • Pregnant or nursing, or planning on becoming pregnant over the next 9 months.
  • Planning to relocate in the next 9 months
  • Involvement in another research study that would interfere with participation in this study
  • Excessive alcohol intake or dependence
  • Recent weight loss of ≥ 5 kg in the previous 6 months.
  • Report health problems that make weight loss or unsupervised exercise unsafe or unreasonable (e.g., orthopedic limitations, heart problems, history or heart attack or stroke)
  • History of clinically diagnosed eating disorder.
  • Untreated thyroid disease or and changes in dose or type of thyroid medication over previous 6 months
  • Chronic/inflammatory gastrointestinal disorders (Irritable Bowel Syndrome acceptable)
  • Taking any prescription medication with known effects on appetite or weight
  • Previous surgical procedure for weight loss.
  • Major surgery within the previous 6 months.
  • Resting systolic blood pressure >160 mmHg or resting diastolic blood pressure >100 mmHg
  • Diuretic use over 1.5mg per day
  • Diagnosis of type 1 or type 2 diabetes
  • Presence of implanted cardiac defibrillator or pacemaker.
  • History of presence of cancer within past 5 years or current treatment for cancer (completely resected basal or squamous cell carcinoma acceptable if treatment

Sites / Locations

  • University of North Carolina at Chapel Hill

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Modified Weight Watchers plan

Arm Description

Modified Weight Watchers Plan which includes a food plan, activity plan, group support and cognitive behavior modification. Weekly study-specific group meetings; electronic tools through iPhone app for 24 weeks.

Outcomes

Primary Outcome Measures

Weight Change
Mean Change in body weight (kg) Body weight will be assessed on a calibrated digital scale and recorded to the nearest 0.1 kg.

Secondary Outcome Measures

Achieving a weight loss of 5% or more
% participants achieving a weight loss of 5% initial body weight or more
Achieving a weight loss of 5% or more
% participants achieving a weight loss of 5% initial body weight or more
Weight Change
Mean Change in body weight (kg)
Waist circumference change (cm) (mean)
Waist circumference will be measured at the iliac crest
Waist circumference change (cm) (mean)
Waist circumference will be measured at the iliac crest
Relationship between fitness, flexibility and psychosocial measures with weight change
The relationship between weight change and any of these measures will be assessed.

Full Information

First Posted
January 27, 2017
Last Updated
May 17, 2018
Sponsor
University of North Carolina, Chapel Hill
Collaborators
Weight Watchers International
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1. Study Identification

Unique Protocol Identification Number
NCT03037567
Brief Title
Evaluation of a Commercial Program on Weight Loss and Health Outcomes
Official Title
Evaluation of a Commercial Program on Weight Loss and Health Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
January 27, 2017 (Actual)
Primary Completion Date
August 31, 2017 (Actual)
Study Completion Date
August 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
Weight Watchers International

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to examine the acceptability and efficacy of a modified Weight Watchers program over 24 weeks. Assessments will be conducted at 0, 3, and 6 months.
Detailed Description
The following assessment measures will be taken at 0, 3, and 6 months: Weight measurements. Weight will be taken according to the National Health and Nutrition Examination survey anthropometry procedures manual. Weight will be measured in kilograms to the nearest 0.1 kg using a calibrated digital scale (Tanita, Inc.) with participants in light clothing and no shoes. Two measurements will be taken. and if the measures differ by more than 0.2 kg, a third measure will be taken. An average of the closest two measures will be calculated and used for data entry. Waist circumference. Waist circumference will be assessed at baseline, 3 and 6 months. Waist circumference will be taken according to the National Health and Nutrition Examination survey anthropometry procedures manual. Measurements will be taken to the nearest 0.1cm, at the top of the pelvis ilium (just above the hip bone) with a non-stretchable tape measure, without compressing the skin, at the end of normal expiration. Two measurements will be taken with a third if the first two do not fall within 0.5 cm. Aerobic stamina. Aerobic stamina will be assessed using the 6 minute walk test. Distance traveled in meters (m) is the outcome. Flexibility. Flexibility will be assessed with the Classic Sit and Reach Test and reported in inches less than or greater than reached on a 20 inch reference mark as measured on a yard stick placed between the legs. Food Cravings. The Food Craving Inventory-II (FCI-II) is a validated self-report measure for general cravings and cravings for specific types of foods and will be completed at baseline, Months 3 and 6. Respondents rate the frequency of cravings since the last time they completed the survey for each of 33 food items using a five-point Likert scale (1, never; 2, rarely; 3, sometimes; 4, often; 5, always/almost every day). The FCI-II consists of 5 scales (sweets, high fats, carbohydrates/starches, fast food fats, and fruits & vegetables) that constitute the higher order construct of food cravings (the total score). Happiness. The Oxford Happiness Questionnaire will be used to assess happiness at 0, 3, and 6 months. The OHQ is a validated self-report measure for broad personal happiness. Respondents rate 29 sentences on a 6 point Likert scale (1, strongly disagree; 6, strong agree). Sleep. Participants will be asked to complete the Pittsburgh Sleep Quality Index (PSQI) to assess sleep quality and duration at 0, 3, 6. The PSQI is a validated self-report measure of sleep duration and sleep quality. The PSQI examines seven components of sleep quality retrospectively over a period of four weeks: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction over the last month. The patient self-rates each of these seven areas of sleep. Scoring of answers is based on a 0-3 scale, whereby '3' reflects the negative extreme on the Likert scale. The global score is generated by summing up all seven component scores and ranges from 0 to 21, with higher values corresponding to reduced sleep quality. Weight related quality of life. The Impact of Weight on Quality of Life-Lite (IWQOL-Lite) is a validated self-report measure for an individual's perception of how their weight affects their day-to-day life. Respondents rate the degree to which their weight affects them on 31 items using a five-point Likert scale (1, never true; 2, rarely true; 3, sometimes true; 4, usually true; 5, always true). The IWQOL-Lite consists of 5 scales (physical function, self-esteem, sexual life, public distress, and work). Perceived Hunger. The Visual Analogue Scale (VAS) measures sensations that range across a continuum of values and cannot be easily directly measured. Operationally, the VAS is a horizontal line measuring exactly 100 mm in length, anchored by word descriptors (i.e., Not at all hungry, Extremely hungry) at each end. Participants will be asked to complete a three item VAS by placing a mark on the line at the point they feel represents their response to the question. Program Satisfaction. The Satisfaction Survey is a self-administered survey with 25 items scored on a 5-point Likert scale. This measure will be completed at only at 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight and Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
152 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Modified Weight Watchers plan
Arm Type
Experimental
Arm Description
Modified Weight Watchers Plan which includes a food plan, activity plan, group support and cognitive behavior modification. Weekly study-specific group meetings; electronic tools through iPhone app for 24 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Modified Weight Watchers plan
Intervention Description
Weight Watchers is a structured lifestyle modification program that includes a food plan based on balanced diet and healthy eating, activity plan designed to promote progressive physical activity increase, group support and cognitive behavior modification. Participants attend weekly in-person group meetings led by a trained Weight Watchers meeting leader and have a suite of electronic tools available through an iPhone app.
Primary Outcome Measure Information:
Title
Weight Change
Description
Mean Change in body weight (kg) Body weight will be assessed on a calibrated digital scale and recorded to the nearest 0.1 kg.
Time Frame
0 - 6 months
Secondary Outcome Measure Information:
Title
Achieving a weight loss of 5% or more
Description
% participants achieving a weight loss of 5% initial body weight or more
Time Frame
0 - 6 months
Title
Achieving a weight loss of 5% or more
Description
% participants achieving a weight loss of 5% initial body weight or more
Time Frame
0 - 3 months
Title
Weight Change
Description
Mean Change in body weight (kg)
Time Frame
0 - 3 months
Title
Waist circumference change (cm) (mean)
Description
Waist circumference will be measured at the iliac crest
Time Frame
0 - 3 months
Title
Waist circumference change (cm) (mean)
Description
Waist circumference will be measured at the iliac crest
Time Frame
0 - 6 months
Title
Relationship between fitness, flexibility and psychosocial measures with weight change
Description
The relationship between weight change and any of these measures will be assessed.
Time Frame
0 - 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Body mass index (BMI) between 25 and 43 kg/m² Ability to read and speak English All ethnic groups will be recruited Self-report desire to lose weight and willing to follow study recommendations Use of an iPhone with iOS 8.0 or later for use on a daily basis, and basic app skills Have access to the internet via a computer, and basic computer skills Exclusion Criteria: Currently following a commercial weight-loss program (including Weight Watchers) or who followed a weight loss program in the previous 6 months or who were members of Weight Watchers within the past 12 months Another member of the household participating in the study. Pregnant or nursing, or planning on becoming pregnant over the next 9 months. Planning to relocate in the next 9 months Involvement in another research study that would interfere with participation in this study Excessive alcohol intake or dependence Recent weight loss of ≥ 5 kg in the previous 6 months. Report health problems that make weight loss or unsupervised exercise unsafe or unreasonable (e.g., orthopedic limitations, heart problems, history or heart attack or stroke) History of clinically diagnosed eating disorder. Untreated thyroid disease or and changes in dose or type of thyroid medication over previous 6 months Chronic/inflammatory gastrointestinal disorders (Irritable Bowel Syndrome acceptable) Taking any prescription medication with known effects on appetite or weight Previous surgical procedure for weight loss. Major surgery within the previous 6 months. Resting systolic blood pressure >160 mmHg or resting diastolic blood pressure >100 mmHg Diuretic use over 1.5mg per day Diagnosis of type 1 or type 2 diabetes Presence of implanted cardiac defibrillator or pacemaker. History of presence of cancer within past 5 years or current treatment for cancer (completely resected basal or squamous cell carcinoma acceptable if treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deborah F Tate, PhD
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27514
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Evaluation of a Commercial Program on Weight Loss and Health Outcomes

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