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Lifestyle Intervention Program in Overweight Medical Students

A Novel Lifestyle Intervention Program to Improve Body Composition and Chronic Disease Bio Markers in Overweight Medical Students: a Randomized Cross-over Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03636581
Enrollment
40
Registered
2018-08-17
Start date
2018-08-08
Completion date
2021-04-25
Last updated
2022-01-18

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

Conditions

Overweight

Brief summary

This study will be a randomized cross-over design over the course of 2 academic years. 40 subjects -20 overweight women and 20 over weight men will be recruited. Each subject will have body composition tested, blood lipid profile, and resting metabolic rate done in the beginning of the first academic year and at the end of the first academic year. The intervention group will receive activity trackers, diet counseling, and fitness counseling for one academic year. The second year, all outcome measures (a body scan, blood lipid profile, and resting metabolic rate) will be performed again at the start of the academic year 2, except the intervention group will now be the control group and the control group will now receive the same intervention. All final outcome measures will be performed at the end of the second year.

Interventions

BEHAVIORALLifestyle counseling

This group will receive online education modules to educate them on exercise prescription, nutrition and behavioral changes.

Sponsors

New York Institute of Technology
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Male and female NYITCOM students between the ages of 18-35 * BMI ≥ 25.0 * Body fat % \>19% for males; \>33% for women (will be determined by body composition scan) * Own their own smartphone

Exclusion criteria

* People who have used weight loss smartphone applications in the past 6 month * People who have used an activity tracker in past 6 months * Anyone who answers yes to one or more questions on the PAR-Q screen * Any contraindication to having a duel x-ray body scan performed based on the American College of Radiology's practice guidelines

Design outcomes

Primary

MeasureTime frameDescription
Body fat percentage4 monthsBody composition

Secondary

MeasureTime frameDescription
Step Count4 monthsActivity based on step count
Resting Metabolic Rate4 monthsResting metabolic rate changes as per oxygen consumption
Total Cholesterol4 monthsfasting serum mg/dL
High Density Lipoproteins4 monthsfasting serum mg/dL
Low Density Lipoproteins4 monthsfasting serum mg/dL
Triglycerides4 monthsfasting serum mg/dL
Hemoglobin A1C4 monthsfasting plasma % of total hemoglobin

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026