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Preventing Overweight in USAF Personnel: Minimal Contact Program

Preventing Overweight in USAF Personnel: Minimal Contact Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00417599
Enrollment
500
Registered
2007-01-01
Start date
2001-12-31
Completion date
2015-11-30
Last updated
2016-06-24

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

Conditions

Obesity, Overweight

Keywords

Prevention of overweight, Prevention of obesity, Treatment of overweight, Treatment of obesity

Brief summary

The prevalence of overweight in the United States Air Force (USAF) is about 22%. The objective of this study is to compare the effectiveness of a minimal contact behavioral therapy plus usual care group(MCBT+UC) using a controlled experimental comparison of usual care(UC). Subjects are USAF personnel who are 5lbs below their Maximum Allowable Weight (MAW) and heavier. The primary hypothesis is that: MCBT+UC will have significant weight loss as compared to UC.

Detailed description

The objective of this study is to compare the relative effectiveness of two approaches to weight management, using a controlled comparison experiment. The two approaches are: Minimal Contact Behavior Therapy Plus Usual Care (MCBT+UC) which includes an orientation meeting, provision of a self-help book, use of an interactive weight management web site for 6 months, and 2 brief motivational interviewing telephone follow-ups, plus usual care;and Usual Care (UC) which includes and orientation meeting and usual care (consisting of required USAF annual physical and fitness exam, participation in any mandatory weight loss or fitness programs, and the requirement to stay below a Maximum Allowable Weight \[MAW\], with penalties or separation as potential contingencies for failure to remain below MAW). The primary outcome is weight loss.Additional outcomes include body mass index, percent body fat, and waist circumference.

Interventions

BEHAVIORALLifestyle Intervention

lifestyle intervention .

OTHERcontrol group

waiting list control group

Sponsors

United States Department of Defense
CollaboratorFED
Baylor College of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Within 5 pounds below or equal to their MAW or above MAW according to USAF Weight and height tables * Access to personal computer with Internet access * Plan to remain in the local area for one year * Male or female between the ages 18-55 years

Exclusion criteria

* Pregnant, planning to become pregnant or becomes pregnant * Weight loss of more than 10 pounds in the past 3 months * No prescription or nonprescription weight-loss medication for at least 6 months prior to screening * On any medical profile. Specific exclusion includes history of myocardial infarction, stroke, or cancer in the past 5 years, diabetes, angina, and orthopedic or joint problems that would prohibit exercise.

Design outcomes

Primary

MeasureTime frame
Body Weight1 year

Secondary

MeasureTime frame
Body Mass Index1 year
Percent Body Fat1year
Waist Circumference1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 6, 2026