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N/A N=122 Randomized Prevention

Effectiveness of a Group Lifestyle Balance Class in a Military Population

Primary Prevention

Enrolled (actual)
122
Serious AEs
0.0%
Results posted
Jul 2020
Primary outcome: Primary: Weight — 191.47; 198.08; 204.08 pounds

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Group Lifestyle Balance (Behavioral); Better Body Better Life (Behavioral); Fitness Improvement Program (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
David Grant U.S. Air Force Medical Center
Primary completion
Oct 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Weight
191.47; 198.08; 204.08
PRIMARY
Abdominal Circumference
34.96; 35.68; 36.09
SECONDARY
Well-being
77; 82; 76
SECONDARY
Lipids
188.17; 180.52; 170.67
SECONDARY
Physical Activity
45; 50; 45
SECONDARY
HbA1C
5.26; 5.22; 5.26

Summary

With this study researchers will evaluate the effects of the GLB intervention on weight loss, chronic disease indicators and self-perceived function and well-being in an active duty population. The purpose of this study is to examine the effectiveness of the GLB program [compared with two currently available programs, the Fitness Improvement Program (FIP) and the Better Body Better Life (BBBL) program], on the following health indicators: improvement of individual physical fitness as measured by change in abdominal circumference, weight and physical activity; decrease in risk associated with chronic disease as measured by changes in lipid and HbA1c levels; and improvement in self-perceived function and well-being as measured by the RAND 36 Item Short Form Health Survey (RAND SF- 36). In addition, the researchers seek to obtain feedback about the programs from the participants.

Eligibility Criteria

Inclusion Criteria

  • • An active duty member of the USAF
  • Have at least one of the following conditions:
  • An abdominal circumference over 35 inches for men or 31.5 inches for women
  • BMI over 25 kg/m2
  • Are willing to commit to weekly 1 hour classes for 12 weeks and monthly 1 hour classes for an additional 3 months

Exclusion Criteria

  • • Women who are pregnant or breastfeeding
  • Participants who are within 8 months of a Permanent Change of Station or deployment
  • Anyone who has been restricted from participating in moderate activity equivalent to a brisk walk
  • Taking lipid-lowering or glucose-lowering medication
  • Anyone who for medical reasons cannot have a calorie-restricted diet
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02556112). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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