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A Study Of Starting Strength Barbell Training

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Mayo Clinic

Status

Enrolling

Conditions

Lipid Profile
Fasting Glucose
Blood Pressure

Treatments

Other: Progressive Barbell Strength Training

Study type

Interventional

Funder types

Other

Identifiers

NCT07578285
26-001184

Details and patient eligibility

About

The purpose of this study is to determine the effect of a 12-week coached Starting Strength barbell training program on systolic and diastolic blood pressure.

Enrollment

200 estimated patients

Sex

All

Ages

15 to 100 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Adults aged 18-100 years
  • Sedentary or minimally active (less than 150 minutes of moderate-intensity physical activity per week)
  • No participation in structured resistance training programs within the past 6 months.
  • Able to safely participate in resistance training as determined by medical screening
  • Willing to commit to 3 training sessions per week for 12 weeks
  • Able to provide informed consent
  • Willing to obtain pre- and post-intervention laboratory tests from the same laboratory company.

Exclusion criteria

  • Current participation in structured resistance training programs
  • Cardiovascular disease requiring activity restriction
  • Uncontrolled hypertension (systolic BP >180 mm Hg or diastolic BP >110 mm Hg)
  • Musculoskeletal conditions precluding safe barbell training
  • Changes in lipid-lowering or antihypertensive medications within 3 months prior to enrollment
  • Known cardiovascular, metabolic, or renal disease that would preclude safe participation in resistance training

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

Starting Strength barbell training program
Experimental group
Description:
12-week coached, progressive overload barbell strength training program (Starting Strength)
Treatment:
Other: Progressive Barbell Strength Training

Trial contacts and locations

1

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Central trial contact

Joshua Lee, PA-C,MPAS

Data sourced from clinicaltrials.gov

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