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Dissemination of the Look Ahead Weight Management Treatment in the Military

Dissemination of the Look Ahead Weight Management Treatment in the Military

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02063178
Acronym
FITBLUE
Enrollment
248
Registered
2014-02-14
Start date
2014-01-06
Completion date
2018-06-30
Last updated
2019-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight, Obesity

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.

Interventions

BEHAVIORALPhone-based sessions (28 total) on a structured schedule

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.

BEHAVIORALPhone-based sessions upon request

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.

BEHAVIORALWeight self-monitoring

Each randomized participant will be given a Body Trace scale that will electronically record their weight.

BEHAVIORALDietary and physical activity self-monitoring

Each randomized participant will be given a free account to Lose It! Premium, an online food/activity diary for self-monitoring.

BEHAVIORALScheduled tailored interventionist feedback

Randomly assigned participants to the counselor-initiated condition will receive feedback on their progress throughout their sessions with their assigned interventionist.

BEHAVIORALDietary goals

Each randomized participant will receive a daily calorie goal range based on their current weight, gender, and BMI.

Randomized participants will receive coupons for meal replacements including oatmeal and popcorn.

BEHAVIORALPhysical activity goals

Each participant will complete the Global Physical Activity Questionnaire which will determine their weekly exercise goals.

BEHAVIORALToolbox

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.

BEHAVIORALChallenges

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.

BEHAVIORALTailored interventionist feedback upon request

Randomly assigned participants to the self-paced condition have the option to receive feedback on their progress upon request.

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
United States Air Force
CollaboratorFED
University of Tennessee
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Percent Weight Loss (Baseline to 12 Months)12 month interventionThe 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

MeasureTime frameDescription
The Relationship Between Attendance and Percent Weight Loss12 month interventionEvaluating 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 Loss12 month interventionWe 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 Loss12 month interventionWe will also evaluated the impact of self-weighing (using Body Trace e-scales) on weight loss outcomes.

Countries

United States

Participant flow

Participants by arm

ArmCount
Counselor-Initiated
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. Phone-based sessions (28 total) on a struct
124
Self-Paced
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.
124
Total248

Baseline characteristics

CharacteristicCounselor-InitiatedSelf-PacedTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
124 Participants124 Participants248 Participants
Age, Continuous35.3 years
STANDARD_DEVIATION 8.2
33.8 years
STANDARD_DEVIATION 6.8
34.6 years
STANDARD_DEVIATION 7.5
Ethnicity (NIH/OMB)
Hispanic or Latino
25 Participants31 Participants56 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
99 Participants93 Participants192 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
African American
26 Participants23 Participants49 Participants
Race/Ethnicity, Customized
Caucasian
79 Participants84 Participants163 Participants
Race/Ethnicity, Customized
Other
19 Participants17 Participants36 Participants
Region of Enrollment
United States
124 participants124 participants248 participants
Sex: Female, Male
Female
61 Participants61 Participants122 Participants
Sex: Female, Male
Male
63 Participants63 Participants126 Participants
Weight88.0 kg
STANDARD_DEVIATION 12.9
90.0 kg
STANDARD_DEVIATION 15.5
89.0 kg
STANDARD_DEVIATION 14.3

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 1240 / 124
other
Total, other adverse events
75 / 12455 / 124
serious
Total, serious adverse events
5 / 1245 / 124

Outcome results

Primary

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.

Time frame: 12 month intervention

ArmMeasureValue (MEAN)Dispersion
Counselor-InitiatedPercent Weight Loss (Baseline to 12 Months)2.1 percent weight lossStandard Deviation 4.7
Self-PacedPercent Weight Loss (Baseline to 12 Months)0.0 percent weight lossStandard Deviation 4
Comparison: This randomized clinical trial was designed to have 90% power to detect a 4% weight loss percent difference at 12 months between the two study arms.p-value: <0.001Wilcoxon (Mann-Whitney)
Secondary

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.

Time frame: 12 month intervention

ArmMeasureValue (NUMBER)
Counselor-InitiatedThe Relationship Between Attendance and Percent Weight Loss0.49 spearman rho correlation
Self-PacedThe Relationship Between Attendance and Percent Weight Loss-0.10 spearman rho correlation
Comparison: The association between weight change percent and attendance was described using Spearman rank correlation.p-value: <0.0001Correlation
Secondary

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.

Time frame: 12 month intervention

ArmMeasureValue (NUMBER)
Counselor-InitiatedThe Relationship Between Dietary and Physical Activity Self-monitoring Adherence and Percent Weight Loss0.41 Spearman's rho correlation
Self-PacedThe Relationship Between Dietary and Physical Activity Self-monitoring Adherence and Percent Weight Loss0.05 Spearman's rho correlation
p-value: <0.0001Correlation
Secondary

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.

Time frame: 12 month intervention

ArmMeasureValue (NUMBER)
Counselor-InitiatedThe Relationship Between Self-weighing on Weight Loss0.41 spearman's rho correlation
Self-PacedThe Relationship Between Self-weighing on Weight Loss-0.11 spearman's rho correlation
p-value: <0.0001Correlation

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026