Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Healthy Lifestyle
  • Men
  • Obese
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Sequential AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 40 years
Gender
Only males

Description

The investigators will recruit 20 normal weight, active men and 80 obese, inactive men to compare their sperm epigenome at their baseline state. The investigators will randomize the 80 obese, inactive men to intervention or no intervention for 12 weeks:1) observation with clinic visits; 2) low fat/l...

The investigators will recruit 20 normal weight, active men and 80 obese, inactive men to compare their sperm epigenome at their baseline state. The investigators will randomize the 80 obese, inactive men to intervention or no intervention for 12 weeks:1) observation with clinic visits; 2) low fat/low caloric diet; 3) supervised periodized strength and endurance training; and 4) low fat/ low caloric diet plus exercise training. The investigators will compare changes in their sperm epigenome within each group before and after intervention, between groups after intervention including the non-obese,active men at baseline. The investigators will follow the 80 men in the intervention groups and re-examined their sperm epigenome at 12 weeks and then another 24 weeks after cessation of treatment.

Tracking Information

NCT #
NCT04175678
Collaborators
National Institutes of Health (NIH)
Investigators
Principal Investigator: Christina Wang, MD The Lundquist Institute