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NCT Number: NCT06806670

Exercise and Diet Effects in Reducing Cardiovascular Risk in Kidney Transplant Recipients

The goal of this clinical trial is to assess whether, over an observation period of 3 years, there is a reduction in cardiovascular risk, and the extent of this reduction, in a group of adult kidney transplant patients undergoing tailored exercise combined with dietary counselling compared to a group of patients following the 'standard of care'.

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Key information

Age range

30 year–69 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, BO, 40138, Italy

Location status: Recruiting

Location contact

Giuseppe Tarantino, MD

CONTACT

[email protected]

0512144912

Giuseppe Tarantino, MD

PRINCIPAL_INVESTIGATOR

Valentina Totti, PhD

CONTACT

[email protected]

Valentina Totti, PhD

SUB_INVESTIGATOR

About this study

The main questions it aims to answer are:

  • Prescribed exercise and dietary counselling could reduce of at least 1% in the cardiovascular risk score (by Framingham score) and cardiovascular biomarkers in kidney transplant recipients?
  • How much can a lifestyle intervention affect kidney function, quality of life and the gut microbiota in this patient population?

Researchers will compare kidney transplant recipients undergoing tailored exercise combined with dietary counselling compared to a group of patients following the 'standard of care' to see if there is a reduction in cardiovascular risk, BMI, inflammatory markers, improve of gut microbiota and perception of quality of life. In addition, a number of hospital admissions for important clinical events, the number of fatal and non-fatal cardiovascular events (MACE), and mortality from all causes will be assessed in the long term.

Participants will enroll from the Nephrology, Dialysis and Transplant Units and randomize in intervantion group (A) or control (B).

In group A/intervention, a tailored exercise programme combined with specific dietary counselling will be prescribed, in group B/control, generic advice on healthy lifestyles will be given (standard of care) without specific prescription.

In all patients, quality of life, gut microbiota, inflammatory and cardiovascular biomarkers (Framingham score, BNP, etc.), lipid profile and renal function over time will be assessed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinically stabilised male and female kidney transplant patients (assessment by the referring transplant centre)
  • Minimum age, 30 years;
  • Maximum age, 69 years;
  • Period since transplantation: from 6 months (subject to clinical stability being achieved) to 10 years;
  • Organ function: eGFR (CKD-EPI formula) ≥ 30 mL/min/1.73m ;2
  • Obtaining informed consent;

Exclusion criteria

  • Patients unable to follow the prescription,
  • Recent acute cardiovascular event (< 2 months),
  • Unstable angina,
  • Hyperkinetic/hypokinetic arrhythmias not controlled by therapy, and with signs of haemodynamic impairment,
  • Severe aortic stenosis,
  • Heart failure NYHA class III-IV, FE < 40%,
  • Acute illnesses that limit physical activity,
  • Severe hypertension (basal BP ≥200/110 mm Hg),
  • Neuro-musculo-skeletal pathologies that may be aggravated by exercise,
  • Patients unwilling to change lifestyle;
  • Any form of substance abuse, psychiatric disorder or condition that, according to the investigator, can complicate communication between doctor and patient;
  • Pregnant women.

Treatment and study plan

Lifestyle Intervention

Behavioral

exercise and dietary counselling

Primary outcomes

  1. Cardiovascular risk reduction

    Time frame: From enrollment to the end of the treatment (3 years)

    reduction of at least 1% in the cardiovascular risk score - Framingham score - over the observation time. This score estimates the risk of developing a cardiovascular event over a 10-year period and is calculated in relation to the outcome from the following identifiable variables in normal clinical practice:

    • Sex
    • Age
    • Systolic pressure value
    • Treatment for hypertension (yes/no)
    • Smoker (yes/no)
    • Diabetes (yes/no)
    • HDL value
    • Total cholesterol value

Secondary outcomes

  1. Renal function

    Time frame: From enrollment to the end of the treatment (3 years)

    The trend of renal function assess by eGFR using the CKD-EPI formula

  2. Gut microbiota analysis

    Time frame: From enrollment to the end of the treatment (3 years)

    The relative abundances of the main intestinal bacterial groups and hence the effect of physical exercise on the gut microbiota

  3. Inflammatory status

    Time frame: From enrollment to the end of the treatment (3 years)

    The variation of the inflammatory status (by CRP analysis, IL-6, ferritin, cortisol)

  4. Quality of Life (QoL)

    Time frame: From enrollment to the end of the treatment (3 years)

    The perception of quality of life through the SF12 questionnaire (composite items of physical and mental health)

  5. Adherence to the lifestyle intervention

    Time frame: From enrollment to the end of the treatment (3 years)

    Adherence to dedicated counseling through IPAQ questionnaire to assess physical activity and food frequency questionnaire to assess diet

  6. Cost-effectiveness of a healthy lifestyle intervention

    Time frame: From enrollment to the end of the treatment (3 years)

    number of hospital admissions for major clinical events

  7. Cardiovascular biomarkers

    Time frame: From enrollment to the end of the treatment (3 years)

    the trend of biomarkers related to cardiovascular risk (lipid profile, BNP)

Study contacts

Contact information is provided by the study sponsor or research team.

Giuseppe Tarantino, MD

CONTACT

[email protected]

0512144912

Valentina Totti, PhD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Collaborators

  • Azienda Unità Sanitaria Locale della Romagna
  • CNT (Centro Nazionale Trapianti)

Registry information

Official study title

Effects of Exercise and Dietary Counselling in Reducing the Cardiovascular Risk Score in Kidney Transplant Patients: KT- LIFESTYLE Study

Acronym: KT-LIFESTYLE

Important dates

Study start
2025
Primary completion
2030
Study completion
2031
First posted
Feb 4, 2025
Registry last updated
Feb 4, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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