Healthy Eating, Activity, & Lifestyle Training Headquarters: II Pilot Project

Pennington Biomedical Research Center

Status: Completed

Conditions: Weight Loss; Overweight

Treatments: Behavioral: H.E.A.L.T.H. II Intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT02905422

PBRC 2015-013

Details and patient eligibility

About

The proposed study aims to combine evidenced based tools and guidance (H.E.A.L.T.H.: Healthy Eating Activity Lifestyle Training Headquarters) previously tested that has been developed specifically for use by Army Soldiers and a remote clinical intervention model that includes mobile tracking technology/devices for physical activity, weight and nutrition. This program is called the H.E.A.L.T.H. Intensive.

Full description

The purpose of this investigation is to test the efficacy of a remote intervention to assist Soldiers in meeting standards for body fat and fitness. The intervention will include:

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.

Enrollment: 80 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Male and Female Soldiers who are members of the Louisiana National Guard

   • 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

1. Soldiers and family members younger than 18 years of age
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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Single Blind

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80 participants in 2 patient groups

Waitlist Control Group

No Intervention group

Description:

Six month delayed access to the H.E.A.L.T.H. II Intervention - Intensive intervention (wait-list control)

Active Intervention Group

Active Comparator group

Description:

Immediate access to the H.E.A.L.T.H. II Intervention - Intensive intervention

Treatment:

Behavioral: H.E.A.L.T.H. II Intervention