Menu
Recruiting NCT06212063

Aim High: Readiness & Meeting the Standards in Military Pre-Recruits

No phase Interventional Health Behavior

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Cadet Health.
Who it may be relevant to
Registry conditions: Health Behavior. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The primary objective of the proposed study is to complete a comprehensive needs assessment of the Louisiana National Guard (LANG) Youth Challenge Program (YCP) in the YCP leadership and junior cadet population related to nutrition, fitness, sleep, and mental health and resilience. Results of this needs assessment will further inform the development of the intervention skills training program. The secondary objective of this work is to provide a scalable, integrated physical and mental optimization training program that would be integrated into relevant systems and maintained over time as a core tool for young individuals readying themselves to join the Army. The program would include an environmental intervention approach as well as nutrition, physical activity, sleep, and stress reduction/positive coping guidance.

Interventions

  • Behavioral Cadet Health
    Integrated physical and mental optimization training program used as tool for young individuals readying themselves to join the military

Primary outcome measures

  • Height [Time frame: 16 Months]
  • Weight [Time frame: 16 Months]
  • Body Fat [Time frame: 16 Months]
  • Depression [Time frame: 16 Months]
  • Anxiety [Time frame: 16 Months]
  • Body Esteem [Time frame: 16 Months]
  • Coping [Time frame: 16 Months]
  • Perceived Stress [Time frame: 16 Months]
  • Eating Competence [Time frame: 16 Months]
Secondary outcome measures (2)
  • Knowledge & Attitudes [Time frame: 16 Months]
  • Program Satisfaction [Time frame: 16 Months]

Eligibility criteria

Inclusion criteria

  • Must be either staff, cadre, or cadets in the YCP program.

Exclusion criteria

  • Not staff, cadre, or cadets in the YCP program.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Other

Study locations

United States · 1 center
  • Pennington Biomedical Research Center — Baton Rouge

Identifiers

NCT: NCT06212063 · PBRC 2023-074

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗