The Effect of Walking in Kidney Transplant Patients

August 6, 2021 updated by: FATMA DEMIR KORKMAZ, Ege University

The Effect of Pedometer Assisted Walking on Physical Activity Level and Metabolic Parameters in Patients With Renal Transplantation

Cardiovascular diseases are among the most common causes of death in kidney transplant patients. Physical activity is of great importance in preventing cardiovascular diseases after transplantation. Although regular physical activity is recommended in international guidelines to prevent post-transplant mortality and morbidity in kidney transplant patients, studies have shown that patients do not follow regular physical activity instructions.The aim of our project is to examine the effect of pedometer-assisted physical activity on metabolic parameters after kidney transplantation.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Patients with kidney transplant surgery will be randomized to the intervention (n: 34) and control groups (n: 34), respectively, according to the transplant surgery date. Intervention and Control groups will be given the same training on the importance of physical activity during discharge training. The pedometer will be given to the intervention group to evaluate the activity level, and it will be said that their goal is to take 2000 steps in 20 minutes a day after discharge. Patients will be asked to carry the pedometer during physical activity, and to write down the number of steps they take in 20 minutes on the form given to them for 90 days. Patients in the control group will only be advised to do physical activity every day and will be asked to record the minutes of physical activity they do for 90 days. Metabolic parameters of the patients in the intervention and control groups will be examined at the end of the 4th and 12th months. These parameters are blood pressure, body mass index, complete blood count (hemoglobin, leukocyte, thrombocyte), blood glucose, sodium, potassium, calcium, liver enzymes, serum creatinine, total and indirect bilirubin, albumin and total cholesterol levels.

Study Type

Interventional

Enrollment (Anticipated)

68

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria: • Over the age of 18 and under the age of 65,

  • Kidney transplantation at the center where the study was conducted between the research dates,
  • There is no activity restriction recommendation by the physician,
  • Patients who agree to participate in the study.

Exclusion Criteria:

  • Multiple organ transplantation at the same time,
  • Death or graft loss/rejection in the hospital before discharge,
  • Patients with physical activity restrictions by the physician,
  • Patients who are re-hospitalized within the first 3 months after discharge

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Using a pedometer
The pedometer will be given to the intervention group to evaluate the activity level and to encourage a walk , it will be said that their goal is to take 2000 steps in 20 minutes a day after discharge. Patients will be asked to carry the pedometer during physical activity, and to write down the number of steps they take in 20 minutes on the form given to them for 90 days.
2000 steps per day in 20 minutes for 90 days, guided by a pedometer after a kidney transplantation
No Intervention: Not using a pedometer
The control group will not be given a pedometer.Patients in the control group will only be instructed to do physical activity every day and will be asked to record the minutes of physical activity they do for 90 days.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Blood Pressure
Time Frame: Change from Baseline Blood Pressure at 4 months after discharge
mmHg
Change from Baseline Blood Pressure at 4 months after discharge
Blood Pressure
Time Frame: Change from Baseline Blood Pressure at 12 months after discharge
mmHg
Change from Baseline Blood Pressure at 12 months after discharge
Body Mass Index (BMI)
Time Frame: Change from Baseline BMI at 4 months after discharge
BMI is weight in kilograms divided by height in meters squared. Formula: weight (kg) / [height (m)]2
Change from Baseline BMI at 4 months after discharge
Body Mass Index (BMI)
Time Frame: Change from Baseline BMI at 12 months after discharge
BMI is weight in kilograms divided by height in meters squared. Formula: weight (kg) / [height (m)]2
Change from Baseline BMI at 12 months after discharge
Hemoglobin
Time Frame: Change from Baseline Hemoglobin at 4 months after discharge
g/dL
Change from Baseline Hemoglobin at 4 months after discharge
Hemoglobin
Time Frame: Change from Baseline Hemoglobin at 12 months after discharge
g/dL
Change from Baseline Hemoglobin at 12 months after discharge
Leukocyte
Time Frame: Change from Baseline Leukocyte at 4 months after discharge
10^3/µL
Change from Baseline Leukocyte at 4 months after discharge
Leukocyte
Time Frame: Change from Baseline Leukocyte at 12 months after discharge
10^3/µL
Change from Baseline Leukocyte at 12 months after discharge
Thrombocyte
Time Frame: Change from Baseline Thrombocyte at 4 months after discharge
10^3/µL
Change from Baseline Thrombocyte at 4 months after discharge
Thrombocyte
Time Frame: Change from Baseline Thrombocyte at 12 months after discharge
10^3/µL
Change from Baseline Thrombocyte at 12 months after discharge
Blood Glucose
Time Frame: Change from Baseline Blood Glucose at 4 months after discharge
mg/dL
Change from Baseline Blood Glucose at 4 months after discharge
Blood Glucose
Time Frame: Change from Baseline Blood Glucose at 12 months after discharge
mg/dL
Change from Baseline Blood Glucose at 12 months after discharge
Sodium
Time Frame: Change from Baseline Sodium at 4 months after discharge
mEq/L
Change from Baseline Sodium at 4 months after discharge
Sodium
Time Frame: Change from Baseline Sodium at 12 months after discharge
mEq/L
Change from Baseline Sodium at 12 months after discharge
Potassium
Time Frame: Change from Baseline Sodium at 4 months after discharge
mEq/L
Change from Baseline Sodium at 4 months after discharge
Potassium
Time Frame: Change from Baseline Sodium at 12 months after discharge
mEq/L
Change from Baseline Sodium at 12 months after discharge
Calcium
Time Frame: Change from Baseline Sodium at 4 months after discharge
mEq/L
Change from Baseline Sodium at 4 months after discharge
Calcium
Time Frame: Change from Baseline Sodium at 12 months after discharge
mEq/L
Change from Baseline Sodium at 12 months after discharge
Serum Creatinine
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
Serum Creatinine
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge
Total Bilirubin
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
Total Bilirubin
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge
Indirect Bilirubin
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
Indirect Bilirubin
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge
High-density lipoprotein (HDL) cholesterol
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
High-density lipoprotein (HDL) cholesterol
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge
Low-density lipoprotein (LDL) cholesterol
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
Low-density lipoprotein (LDL) cholesterol
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge
Aspartate Aminotransferase
Time Frame: Change from Baseline Sodium at 4 months after discharge
U/L
Change from Baseline Sodium at 4 months after discharge
Aspartate Aminotransferase
Time Frame: Change from Baseline Sodium at 12 months after discharge
U/L
Change from Baseline Sodium at 12 months after discharge
Alanine aminotransferase
Time Frame: Change from Baseline Sodium at 4 months after discharge
U/L
Change from Baseline Sodium at 4 months after discharge
Alanine aminotransferase
Time Frame: Change from Baseline Sodium at 12 months after discharge
U/L
Change from Baseline Sodium at 12 months after discharge
Alkaline Phosphatase
Time Frame: Change from Baseline Sodium at 4 months after discharge
U/L
Change from Baseline Sodium at 4 months after discharge
Alkaline Phosphatase
Time Frame: Change from Baseline Sodium at 12 months after discharge
U/L
Change from Baseline Sodium at 12 months after discharge
Triglyceride
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
Triglyceride
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge
Total Cholesterol
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
Total Cholesterol
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge
Albumin
Time Frame: Change from Baseline Sodium at 4 months after discharge
g/dL
Change from Baseline Sodium at 4 months after discharge
Albumin
Time Frame: Change from Baseline Sodium at 12 months after discharge
g/dL
Change from Baseline Sodium at 12 months after discharge
glucose in urine
Time Frame: Change from Baseline Sodium at 4 months after discharge
mg/dL
Change from Baseline Sodium at 4 months after discharge
glucose in urine
Time Frame: Change from Baseline Sodium at 12 months after discharge
mg/dL
Change from Baseline Sodium at 12 months after discharge

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Investigators

  • Principal Investigator: Fatma DEMIR KORKMAZ, Professor, Ege University Faculty of Nursing 35000, Izmir, Turkey

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 19, 2020

Primary Completion (Anticipated)

November 1, 2022

Study Completion (Anticipated)

November 1, 2022

Study Registration Dates

First Submitted

March 30, 2021

First Submitted That Met QC Criteria

August 6, 2021

First Posted (Actual)

August 12, 2021

Study Record Updates

Last Update Posted (Actual)

August 12, 2021

Last Update Submitted That Met QC Criteria

August 6, 2021

Last Verified

August 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • fatma.demir1

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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