Lifestyle overhaul may rewrite Sperm's epigenetic code
NCT ID NCT04175678
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how diet and exercise affect the epigenome—chemical marks on DNA—in sperm of overweight Hispanic men. Researchers will compare sperm from 20 healthy active men and 80 obese inactive men before and after a 12-week program of diet, exercise, or both. They will also check if changes last after stopping the interventions. The goal is to understand if a healthier lifestyle can reverse harmful epigenetic changes that might affect fertility and future children's health.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- diet and exercise
- What this could lead to
- If successful, this could show that lifestyle changes can reverse unhealthy epigenetic marks in sperm, potentially improving fertility and reducing disease risk in children.
- What could go wrong
- This is an early-stage observational and interventional study with only 100 participants, all Hispanic men, so results may not apply to other groups. The long-term health impact on offspring is not directly tested.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2020
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 40 years
- Sex
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Male participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male volunteers in good health as confirmed by physical examination, medical history, and clinical laboratory tests of blood and urine within the reference range at the time of screening 2. Must have Hispanic Father and Mother from Mexico or Central America 3. Normal weight, active subjects: * BMI 18.5 - 24.9 calculated as weight in Kg/ (height in cm)2 * Participates in ≥150 min/week of moderate intensity physical activity as assessed by accelerometer * Consume \< 30% of calories as fat/day * Fasting lipid panel within reference range or not clinically significant above the reference ranges Obese and physically inactive subjects: * BMI ≥ 30 calculated as weight in Kg/ (height in cm)2 in obese subjects * Have risk factors for developing type 2 diabetes (first degree relatives with Diabetes Mellitus type 2, BP≥130/80, HDL-cholesterol ≤ 35mg/dL or triglycerides ≥200mg/dL, fasting plasma glucose ≥100mg/dl to 125mg/dL or HgbA1c ≥ 5.7 to 6.4%, abnormal liver transaminases (not more than 3 times upper limit of normal suggestive of hepatic steatosis) * Participates in ≤150 min/week of moderate intensity physical activity * Consume \>30 % fat as calories/day * Stable weight for past six months prior to the first screening visit * Willing to commit to 12 weeks of three times a week personalized exercise training * Willing to commit to 12 weeks of weight loss diet (low fat and low calories) 4. In the opinion of the investigator, subject is able to comply with the protocol, understand and sign an informed consent and HIPAA form 5. Does not meet any of the exclusion criteria. Exclusion Criteria: 1. Men who meet any of the following criteria are NOT eligible for enrollment in the trial: 2. Men participating in another clinical trial within the last 30 days prior to the first screening visit 3. Men not living in the catchment's area of the clinic or within a reasonable distance from the site 4. Clinically significant abnormal findings at screening except for those stated above for the obese, inactive group 5. Abnormal serum chemistry values, according to local laboratory normal values that indicate chronic liver or kidney dysfunction or that may be considered clinically significant (except for obesity related abnormal laboratory tests including blood glucose, Hgb A1c, liver transaminases, lipids for the obese, active group as stated above). Other abnormal lab values may also be exclusionary, at the discretion of the investigator 6. Sperm concentration below 15 million/mL in more than one of three screening samples 7. Diastolic (D) blood pressure (BP) \> 30 and Systolic (S) BP \> 130 mm Hg for the healthy, non-obese and active group; and diastolic (D) blood pressure (BP) \> 150 and Systolic (S) BP \> 100 mm Hg for the obese, inactive group on in the opinion of the investigator not suitable for exercise training (BP will be taken 3 times at 5 minute intervals and the mean of all measurements be considered) 8. History of hypertension, including hypertension controlled with treatment in the healthy, active group 9. Known history of reproductive dysfunction including vasectomy or infertility 10. Known history of cardiac, renal, hepatic, cardiac or respiratory disease 11. A serious systemic disease such as diabetes mellitus defined by the American Diabetes Association or morbid obesity (body weight greater than 120% of ideal body weight or BMI limitation as above) 12. Known or suspected alcoholism or drug abuse or chronic infections 13. Serious digestive and/or absorptive problems, including inflammatory bowel disease and 14. Chronic food intolerance or diarrhea that preclude adherence to the study diet. 15. Cardiovascular, respiratory or musculoskeletal disease or joint problems that preclude moderate physical activity. 16. Psychiatric disorders (including eating disorders) or conditions that, in the opinion of the investigator, would preclude participation in the study intervention (e.g. untreated major depression or psychosis, substance abuse, severe personality disorder). 17. History of other malignancies except: adequately treated non-melanoma skin cancer
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The Lundquist Institute
Torrance, California, 90502, United States
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