Actively Recruiting
Velocity-Based Resistance Training in Kidney Transplant Recipients
Led by Fundación Universitaria del Area Andina · Updated on 2026-01-27
12
Participants Needed
1
Research Sites
113 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This randomized controlled trial aims to evaluate the effects of velocity-based resistance training on renal function and metabolic health in kidney transplant recipients. Participants will be randomized into two groups performing resistance training at different execution velocities (maximal intended vs. submaximal controlled). The intervention will last 12 weeks and include multi-joint exercises (squat, bench press, military press). Primary outcomes include renal function (serum creatinine, eGFR, blood urea nitrogen, uric acid) and metabolic markers (HDL, triglycerides, glucose, waist circumference, blood pressure). Secondary outcomes include muscle strength, force-velocity profile, anthropometry, physical activity, fitness perception, and adherence to immunosuppressive medication.
CONDITIONS
Official Title
Velocity-Based Resistance Training in Kidney Transplant Recipients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men and women aged 18 to 50 years
- Kidney transplant performed 12 months or more before enrollment
- Stable graft function in the previous 6 months (serum creatinine < 1.5 mg/dL, no rejection episodes)
- Written medical clearance from a nephrologist to perform moderate-to-vigorous physical activity
- Signed informed consent
You will not qualify if you...
- Active autoimmune disorders
- Recent coronary disease (within 6 months)
- Severe musculoskeletal limitations preventing resistance training
- Diagnosis of diabetes mellitus (pre- or post-transplant)
- Current active infection
- Use of immunosuppressive drugs contraindicated for exercise (e.g., mTOR inhibitors at baseline)
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Colombia
Bogotá, Bogota D.C., Colombia, 0000
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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