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Dissemination of the Look Ahead Weight Management Treatment in the Military (FITBLUE)

Primary Purpose

Overweight, Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Phone-based sessions (28 total) on a structured schedule
Phone-based sessions upon request
Weight self-monitoring
Dietary and physical activity self-monitoring
Scheduled tailored interventionist feedback
Dietary goals
Meal replacements
Physical activity goals
Toolbox
Challenges
Tailored interventionist feedback upon request
Sponsored by
University of Tennessee
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overweight

Eligibility Criteria

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

Inclusion Criteria:

  1. Active duty military personnel at Joint Base San Antonio in the San Antonio, Texas area
  2. BMI > 25kg/m2
  3. English speaking
  4. Clearance by healthcare provider for participation in study
  5. >18 years of age
  6. Participants have at least one year left on their duty assignment at enrollment

Exclusion Criteria:

  1. No access to a computer for self-monitoring in Lose It! or email feedback from counselor
  2. Scheduled extended leave away from the San Antonio area in the next 13 months (i.e. planned Permanent Change of Station/Temporary Duty Assignment/deployment)
  3. More than one failure of military-proctored physical fitness test on the last 12 months
  4. Uncontrolled hypertension defined as Blood pressure > 140/90
  5. A member of the same household is already a FitBlue participant
  6. Disability or condition that would limit physical activity
  7. Current use of a weight loss medication
  8. History of significant kidney or liver disease
  9. History of uncontrolled thyroid disease or pheochromocytoma
  10. Malignancy in last 5 years
  11. History of diabetes treated with a medication that could cause hypoglycemia
  12. Pregnancy, child birth within the last 6 months, breastfeeding for less than 6 months postpartum, or planning to become pregnant during the study follow-up time (12 months)
  13. Presence of an unstable psychiatric condition
  14. Severe asthma, bronchitis, or emphysema that precludes exercise
  15. History of bariatric surgery or history of significant recent weight loss ( > 10 pounds in past 3 months)
  16. Other medical or behavioral factors that in the judgement of the Principal Investigator may interfere with study participation or the ability to follow the intervention protocol
  17. History of cerebral, coronary, or peripheral vascular disease, uncontrolled cardiac arrhythmia, or uncontrolled congestive heart failure in past 12 months
  18. Lack of access to telephone

Sites / Locations

  • Wilford Hall Ambulatory Surgical Center/Lackland Air Force Base

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Counselor-Initiated

Self-Paced

Arm Description

Participants will receive 28 telephone sessions over a 12 month period by interventionists trained in behavior change skills and motivational interviewing techniques. Participants will be asked to monitor food intake and physical activity using the LoseIt website/app and weight daily using a Body Trace e-scale. Participants will receive feedback on self-monitoring through e-mail. Dietary goals will be based on weight and participants' weight-loss progress. Participants will be encouraged to replace 2 meals and a snack with meal replacements (provided). Participants will be asked to gradually increase their moderate to vigorous exercise to 225-250 minutes per week. The Toolbox includes additional treatment options (e.g., food scales, exercise videos, cookbooks) for those who wish to take advantage of them. There will be several challenges that will provide a specific goal (e.g. increase self-monitoring), with a small award for completion.

The Self-paced group uses a less intense approach, where the participants can receive the same telephone counseling sessions as the counselor-initiated group, only if they call the counselor. Participants will be asked to monitor food intake and physical activity using the LoseIt website/app and weight daily using a Body Trace e-scale. Participants will receive feedback on self-monitoring through e-mail only upon request. Dietary goals will be based on weight and participants' weight-loss progress. Participants will be asked to gradually increase their moderate to vigorous exercise to 225-250 minutes per week.

Outcomes

Primary Outcome Measures

Percent Weight Loss (Baseline to 12 Months)
The primary data analysis will adhere to the intention-to-treat principle and in the final analysis, the participants will be categorized according to their initial randomization. Investigators will be using the baseline weight as a covariate in the final primary model where the two arms will be compared in terms of the percentage of weight loss.

Secondary Outcome Measures

The Relationship Between Attendance and Percent Weight Loss
Evaluating the impact of intervention session attendance on percent weight loss outcome, as a measure of adherence.
The Relationship Between Dietary and Physical Activity Self-monitoring Adherence and Percent Weight Loss
We will evaluate the impact of dietary and physical activity self-monitoring adherence (using Lose It website/app) on weight loss outcome.
The Relationship Between Self-weighing on Weight Loss
We will also evaluated the impact of self-weighing (using Body Trace e-scales) on weight loss outcomes.

Full Information

First Posted
February 10, 2014
Last Updated
February 6, 2019
Sponsor
University of Tennessee
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), United States Air Force
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1. Study Identification

Unique Protocol Identification Number
NCT02063178
Brief Title
Dissemination of the Look Ahead Weight Management Treatment in the Military
Acronym
FITBLUE
Official Title
Dissemination of the Look Ahead Weight Management Treatment in the Military
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
January 6, 2014 (Actual)
Primary Completion Date
March 2017 (Actual)
Study Completion Date
June 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Tennessee
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), United States Air Force

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Purpose: This study aims to take the procedural and research-based lessons learned from a pilot weight loss intervention (IRB # 13-02563-XP), conducted by The University of Tennessee Health Science Center in 2013, and apply them to the current study of 204 active duty military personnel. The pilot study translated and tailored the Look Ahead weight loss intervention to an overweight/obese active duty U.S. Air Force population, while accommodating the lifestyle and environment that is unique to military members and evaluate materials and procedures used. Rationale: Being overweight is now by far the leading medical reason for rejection in the military. Unfortunately, the impact of weight problems on the military does not stop with those turned away from military service. From 1998 to 2008, the Armed Forces Health Surveillance Center reported the percent of active military members who experienced medical encounters for overweight or obesity significantly increased. The estimated total days of work lost from absenteeism associated with active-duty personnel who are overweight or obese was 658,000. Using Department of Defense (DOD) estimates of average daily based, it was estimated that overweight and obesity costs the DOD $103 million dollars in health care costs annually. Note this estimate is for active duty personnel only. Furthermore, obesity is a major cause for the discharge of uniformed personnel. The current study is inspired by the successful Look Ahead trial, a behavioral science obesity intervention treatment program that included: a collaborative approach, education, behavioral support, and motivational interviewing. The unique nature of this weight reduction study is significant. To our knowledge, there had not been a successful translation of a highly efficacious obesity treatment in the military until The University of Tennessee Health Science Center implemented a pilot version of the Fit Blue program for active duty U.S. Air Force members in 2013. Following a successful pilot and extant results from the Look Ahead trial, Investigators expect success during the full scale Fit Blue study.
Detailed Description
This study is a weight loss intervention program tailored to a military population. Investigators will randomize 204 consented participants to either an intensive counselor-initiated weight loss intervention or a self-paced weight loss intervention. Neither of the aforementioned conditions are controls and both treatments are expected to result in weight reduction. Procedures: This is a two-arm individually randomized trial. The Counselor-initiated group will follow a more intense counselor-initiated approach, where the counselor schedules weekly telephone sessions and contacts them directly. The Self-paced group uses a less intense approach, where the participants can receive the same telephone counseling sessions as the counselor-initiated group, only if they call the counselor. Potential participants will be recruited through the use of advertisements, electronic bulletins, emails, newspapers, and word-of-mouth. Prior to randomization, interested individuals will complete a phone screening, informed consent, two in-person data collection visits and obtain medical clearance, as well as participate in 1 week of dietary and physical activity self-monitoring. The randomized participants will spend the next year involved in study interventions (either the Counselor-Initiated intervention or the Self-Paced intervention), diet and exercise self-monitoring, daily weighing, and may also include telephone counseling sessions. The follow-up data collection visits will occur at 4 and 12 months after randomization. At these visits, physical measurements will be collected (i.e. height, weight, abdominal circumference, blood pressure and heart rate) and participants will complete various questionnaires. A Quality of Life questionnaire will also be administered by study personnel.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
248 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Counselor-Initiated
Arm Type
Experimental
Arm Description
Participants will receive 28 telephone sessions over a 12 month period by interventionists trained in behavior change skills and motivational interviewing techniques. Participants will be asked to monitor food intake and physical activity using the LoseIt website/app and weight daily using a Body Trace e-scale. Participants will receive feedback on self-monitoring through e-mail. Dietary goals will be based on weight and participants' weight-loss progress. Participants will be encouraged to replace 2 meals and a snack with meal replacements (provided). Participants will be asked to gradually increase their moderate to vigorous exercise to 225-250 minutes per week. The Toolbox includes additional treatment options (e.g., food scales, exercise videos, cookbooks) for those who wish to take advantage of them. There will be several challenges that will provide a specific goal (e.g. increase self-monitoring), with a small award for completion.
Arm Title
Self-Paced
Arm Type
Active Comparator
Arm Description
The Self-paced group uses a less intense approach, where the participants can receive the same telephone counseling sessions as the counselor-initiated group, only if they call the counselor. Participants will be asked to monitor food intake and physical activity using the LoseIt website/app and weight daily using a Body Trace e-scale. Participants will receive feedback on self-monitoring through e-mail only upon request. Dietary goals will be based on weight and participants' weight-loss progress. Participants will be asked to gradually increase their moderate to vigorous exercise to 225-250 minutes per week.
Intervention Type
Behavioral
Intervention Name(s)
Phone-based sessions (28 total) on a structured schedule
Intervention Description
28 sessions will be reviewed weekly and then bi-weekly with a trained motivational interviewing counselor for those individuals randomly assigned to the counselor-initiated condition.
Intervention Type
Behavioral
Intervention Name(s)
Phone-based sessions upon request
Intervention Description
For those individuals randomly assigned to the self-paced condition, the 28 sessions are still available to them, the participant has to call to initiate sessions.
Intervention Type
Behavioral
Intervention Name(s)
Weight self-monitoring
Intervention Description
Each randomized participant will be given a Body Trace scale that will electronically record their weight.
Intervention Type
Behavioral
Intervention Name(s)
Dietary and physical activity self-monitoring
Intervention Description
Each randomized participant will be given a free account to Lose It! Premium, an online food/activity diary for self-monitoring.
Intervention Type
Behavioral
Intervention Name(s)
Scheduled tailored interventionist feedback
Intervention Description
Randomly assigned participants to the counselor-initiated condition will receive feedback on their progress throughout their sessions with their assigned interventionist.
Intervention Type
Behavioral
Intervention Name(s)
Dietary goals
Intervention Description
Each randomized participant will receive a daily calorie goal range based on their current weight, gender, and BMI.
Intervention Type
Behavioral
Intervention Name(s)
Meal replacements
Intervention Description
Randomized participants will receive coupons for meal replacements including oatmeal and popcorn.
Intervention Type
Behavioral
Intervention Name(s)
Physical activity goals
Intervention Description
Each participant will complete the Global Physical Activity Questionnaire which will determine their weekly exercise goals.
Intervention Type
Behavioral
Intervention Name(s)
Toolbox
Intervention Description
The toolbox includes additional treatment options for those who wish to take advantage of them. Items may include: food scales, cookbooks, etc. These items may be checked out and must be returned prior to the completion of the study.
Intervention Type
Behavioral
Intervention Name(s)
Challenges
Intervention Description
There will be several challenges designed to increase participant interest and provide a specific goal (e.g., increase self-monitoring). Participants who successfully completed the challenges will be given a small award.
Intervention Type
Behavioral
Intervention Name(s)
Tailored interventionist feedback upon request
Intervention Description
Randomly assigned participants to the self-paced condition have the option to receive feedback on their progress upon request.
Primary Outcome Measure Information:
Title
Percent Weight Loss (Baseline to 12 Months)
Description
The primary data analysis will adhere to the intention-to-treat principle and in the final analysis, the participants will be categorized according to their initial randomization. Investigators will be using the baseline weight as a covariate in the final primary model where the two arms will be compared in terms of the percentage of weight loss.
Time Frame
12 month intervention
Secondary Outcome Measure Information:
Title
The Relationship Between Attendance and Percent Weight Loss
Description
Evaluating the impact of intervention session attendance on percent weight loss outcome, as a measure of adherence.
Time Frame
12 month intervention
Title
The Relationship Between Dietary and Physical Activity Self-monitoring Adherence and Percent Weight Loss
Description
We will evaluate the impact of dietary and physical activity self-monitoring adherence (using Lose It website/app) on weight loss outcome.
Time Frame
12 month intervention
Title
The Relationship Between Self-weighing on Weight Loss
Description
We will also evaluated the impact of self-weighing (using Body Trace e-scales) on weight loss outcomes.
Time Frame
12 month intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active duty military personnel at Joint Base San Antonio in the San Antonio, Texas area BMI > 25kg/m2 English speaking Clearance by healthcare provider for participation in study >18 years of age Participants have at least one year left on their duty assignment at enrollment Exclusion Criteria: No access to a computer for self-monitoring in Lose It! or email feedback from counselor Scheduled extended leave away from the San Antonio area in the next 13 months (i.e. planned Permanent Change of Station/Temporary Duty Assignment/deployment) More than one failure of military-proctored physical fitness test on the last 12 months Uncontrolled hypertension defined as Blood pressure > 140/90 A member of the same household is already a FitBlue participant Disability or condition that would limit physical activity Current use of a weight loss medication History of significant kidney or liver disease History of uncontrolled thyroid disease or pheochromocytoma Malignancy in last 5 years History of diabetes treated with a medication that could cause hypoglycemia Pregnancy, child birth within the last 6 months, breastfeeding for less than 6 months postpartum, or planning to become pregnant during the study follow-up time (12 months) Presence of an unstable psychiatric condition Severe asthma, bronchitis, or emphysema that precludes exercise History of bariatric surgery or history of significant recent weight loss ( > 10 pounds in past 3 months) Other medical or behavioral factors that in the judgement of the Principal Investigator may interfere with study participation or the ability to follow the intervention protocol History of cerebral, coronary, or peripheral vascular disease, uncontrolled cardiac arrhythmia, or uncontrolled congestive heart failure in past 12 months Lack of access to telephone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rebecca Krukowski, PhD
Organizational Affiliation
University of Tennessee
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wilford Hall Ambulatory Surgical Center/Lackland Air Force Base
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78236
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
34259635
Citation
Farage G, Simmons C, Kocak M, Klesges RC, Talcott GW, Richey P, Hare M, Johnson KC, Sen S, Krukowski R. Assessing the Contribution of Self-Monitoring Through a Commercial Weight Loss App: Mediation and Predictive Modeling Study. JMIR Mhealth Uhealth. 2021 Jul 14;9(7):e18741. doi: 10.2196/18741.
Results Reference
derived
PubMed Identifier
33949954
Citation
Fahey MC, Klesges RC, Kocak M, Gladney LA, Talcott GW, Krukowski RA. Counselor Efficiency at Providing Feedback in a Technology-Based Behavioral Weight Loss Intervention: Longitudinal Analysis. JMIR Form Res. 2021 May 5;5(5):e23974. doi: 10.2196/23974.
Results Reference
derived
PubMed Identifier
31773873
Citation
Manz KC, Waters TM, Clifton HE, Kocak M, Klesges RC, Talcott GW, Krukowski RA. Cost-Effectiveness of a Weight Loss Intervention: An Adaptation of the Look AHEAD Lifestyle Intervention in the US Military. Obesity (Silver Spring). 2020 Jan;28(1):89-96. doi: 10.1002/oby.22681. Epub 2019 Nov 26.
Results Reference
derived
PubMed Identifier
31168928
Citation
Pebley K, Klesges RC, Talcott GW, Kocak M, Krukowski RA. Measurement Equivalence of E-Scale and In-Person Clinic Weights. Obesity (Silver Spring). 2019 Jul;27(7):1107-1114. doi: 10.1002/oby.22512. Epub 2019 Jun 5.
Results Reference
derived
PubMed Identifier
30277031
Citation
Fahey MC, Klesges RC, Kocak M, Wayne Talcott G, Krukowski RA. Changes in the Perceptions of Self-weighing Across Time in a Behavioral Weight Loss Intervention. Obesity (Silver Spring). 2018 Oct;26(10):1566-1575. doi: 10.1002/oby.22275.
Results Reference
derived
PubMed Identifier
30277030
Citation
Krukowski RA, Hare ME, Talcott GW, Gladney LA, Johnson KC, Richey PA, Kocak M, Keller PL, Hryshko-Mullen A, Klesges RC. Dissemination of the Look AHEAD Intensive Lifestyle Intervention in the United States Military: A Randomized Controlled Trial. Obesity (Silver Spring). 2018 Oct;26(10):1558-1565. doi: 10.1002/oby.22293.
Results Reference
derived
PubMed Identifier
30125001
Citation
Fahey MC, Hare ME, Talcott GW, Kocak M, Hryshko-Mullen A, Klesges RC, Krukowski RA. Characteristics Associated With Participation in a Behavioral Weight Loss Randomized Control Trial in the U.S. Military. Mil Med. 2019 Mar 1;184(3-4):e120-e126. doi: 10.1093/milmed/usy199.
Results Reference
derived
PubMed Identifier
25545025
Citation
Krukowski RA, Hare ME, Talcott GW, Johnson KC, Richey PA, Kocak M, Balderas J, Colvin L, Keller PL, Waters TM, Klesges RC. Dissemination of the Look AHEAD intensive lifestyle intervention in the United States Air Force: study rationale, design and methods. Contemp Clin Trials. 2015 Jan;40:232-9. doi: 10.1016/j.cct.2014.12.014. Epub 2014 Dec 26.
Results Reference
derived

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Dissemination of the Look Ahead Weight Management Treatment in the Military

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