Healthy Eating, Activity, & Lifestyle Training Headquarters: II Pilot Project
NCT ID: NCT02905422
Last Updated: 2024-12-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
80 participants
INTERVENTIONAL
2016-01-31
2019-04-22
Brief Summary
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Detailed Description
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1. An Internet/Smartphone program for weight management and weight gain prevention developed during previous DoD research.
2. Integrated remote monitoring technology/devices, e.g. smart scales, activity tracking devices.
3. Individualized weight management and exercise recommendations based on data collected from web/mobile app/devices to be delivered via web/mobile app/Smartphone; participants will not travel to a clinical facility for the intervention.
The objectives are:
1. to further develop the H.E.A.L.T.H. intervention by merging components of the H.E.A.L.T.H. program, remote monitoring technology components, e.g. activity tracking devices, smart scales, and direct/individualized weight management and exercise feedback into a single and comprehensive intervention that targets weight and fat loss, improved fitness, improved sleep, and personal well-being for Soldiers and their family members.
2. Compare body weight, body fat, and activity changes associated with participation in the H.E.A.L.T.H Intensive intervention for six months and a six-month website only phase/follow-up phase, in comparison to participation in a wait-list control group; and
3. Evaluate blood biomarkers associated with changes in body weight. Evaluate changes in gut bacteria associated with body weight.
Conditions
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Keywords
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
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Waitlist Control Group
Six month delayed access to the H.E.A.L.T.H. II Intervention - Intensive intervention (wait-list control)
No interventions assigned to this group
Active Intervention Group
Immediate access to the H.E.A.L.T.H. II Intervention - Intensive intervention
H.E.A.L.T.H. II Intervention
12 month study with 6 month intervention phase and 6 month follow up phase. Participants will receive bi-weekly educational information pertaining to weight loss during the intervention phase. Participants will use online website to monitor weight, access meal plans, access weight loss information, and access fitness plans.
Interventions
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H.E.A.L.T.H. II Intervention
12 month study with 6 month intervention phase and 6 month follow up phase. Participants will receive bi-weekly educational information pertaining to weight loss during the intervention phase. Participants will use online website to monitor weight, access meal plans, access weight loss information, and access fitness plans.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Direct family member of the LANG member who is enrolled in the study and will participate with the Soldier
2. ≥18 years old
3. For Soldiers: BMI ≥ 25, AND who exceeds Screening Table Weight AND maximum allowed body fat as outlined by AR600-9 Army regulations For Family Member: BMI ≥ 25
4. Has no known deployments (to the best of their knowledge) for one year upon beginning the study
Exclusion Criteria
2. Soldiers and family members who are pregnant
3. Soldiers and family members who cannot read
4. Soldiers and family members who do not have daily access to wifi
5. Soldiers and family members who do not have access to a smartphone
18 Years
ALL
Yes
Sponsors
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Pennington Biomedical Research Center
OTHER
Responsible Party
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Tiffany Stewart
Associate Professor, Director, Behavior Technology Laboratory
Principal Investigators
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Tiffany Stewart, PhD
Role: PRINCIPAL_INVESTIGATOR
Pennington Biomedical Research Center
Locations
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Pennington Biomedical Research Center
Baton Rouge, Louisiana, United States
Countries
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Other Identifiers
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PBRC 2015-013
Identifier Type: -
Identifier Source: org_study_id