Effect of a Structured Physical Exercise Program on Arteriovenous Fistula Maturation for Hemodialysis in Chronic Kidney Disease Patients
NCT ID: NCT06960304
Last Updated: 2025-05-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
128 participants
INTERVENTIONAL
2025-01-16
2026-06-30
Brief Summary
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Detailed Description
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One of the main issues related to AVFs is primary maturation failure. It is estimated that between 28% and 53% of AVFs experience compromised maturation, which can hinder or even prevent effective long-term cannulation for hemodialysis treatment.
It is well recognized that physical exercise promotes vascular remodeling, as shown by increased capillarity in active muscles, the development of adjacent blood vessels, increased muscle strength, and greater diameter and prominence of veins. Due to its positive influence on vascular remodeling, exercise involving the AVF limb is frequently recommended by international best practice guidelines, and it has the potential to improve the AVF maturation process. However, current scientific evidence does not yet offer a consensus on the most effective type, duration, or intensity of exercise.
Nevertheless, intentional, repetitive, and sustained physical exercise has been shown to lead to vascular remodeling, which may positively impact the functional maturation of an AVF. In this context, the aim is to conduct a quantitative, experimental, and randomized study to evaluate the effect of implementing a Physical Exercise Program for the AVF limb (PEFAV), designed by a rehabilitation nursing specialist, on the AVF maturation process.
As part of the development of the research project titled "Effect of a Structured Physical Exercise Program on Arteriovenous Fistula Maturation", the research team intends to conduct a quantitative, experimental, and randomized study with an expected duration of twenty-four months. The main objective is to evaluate the effect of implementing a Physical Exercise Program for the AVF limb (PEFAV) on the maturation process of the AVF in individuals with stage 5 Chronic Kidney Disease (CKD) who have an upper limb AVF.
Participant recruitment will take place during the specialized nursing clinics for individuals with AV for HD at CHUC - HUC Campus, using a non-probability convenience sampling method. To ensure anonymity and data confidentiality, participants will be randomly assigned to either the Exercise Group (EG) or the Control Group (CG) through a computer-generated randomization sequence using the RedCap software, with a 1:1 allocation ratio.
Two in-person appointments with the participants will be required, both taking place at the specialized nursing clinics for CKD patients with AV for HD at CHUC - HUC Campus. During the first visit, participants will be provided with information about the study's objectives and procedures, and informed consent will be obtained. Following consent, data collection instruments and procedures will be applied. Participants in the EG will receive training and instruction on how to carry out the PEFAV, while those in the CG will receive only the usual recommendations regarding AVF care.
Each participant in the EG will receive a "PEFAV Follow-up Booklet," which will include illustrations and descriptions of the exercises, the number of sets and repetitions, and a section called the "Exercise Log," where participants will be asked to record, after each session, any sensations, perceived changes, or complications related to the AVF, as well as any difficulties performing the exercises.
At the second in-person visit (eight weeks after the first), data collection instruments and procedures will be applied again, and the EG's adherence to the PEFAV will be assessed.
Data collection will include: a questionnaire; grip strength testing and measurements of forearm and arm circumference; and data from the specialized nursing consultation report (physical examination and ultrasound criteria) at CHUC - HUC Campus.
All data collection procedures will follow formal and ethical research standards, ensuring that all informed participants voluntarily, anonymously, consent to take part in the study, with confidentiality maintained and no costs or harm to participants.
The ultimate goal is to increase the number of functional and clinically viable AVFs while reducing associated complications.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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Exercised group
The participants in this group follow a structured physical exercise program for the arm with the Arteriovenous Fistula (AVF), including progressive exercises using weights and therapeutic balls. The goal is to assess the impact of this intervention on AVF maturation and functionality.
Physical exercise program
Evaluation of AVF maturation using clinical and ultrasound criteria, after applying a structured physical exercise program.
Control Group
The participants in this group do not follow the exercise program and only receive the usual recommendations on AVF care (standard of care).
No interventions assigned to this group
Interventions
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Physical exercise program
Evaluation of AVF maturation using clinical and ultrasound criteria, after applying a structured physical exercise program.
Eligibility Criteria
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Inclusion Criteria
* AVF in the upper limb
* No cognitive decline and ability to follow instructions
Exclusion Criteria
* History of injury/condition causing pain or loss of function in the AVF limb
* Musculoskeletal conditions/osteoarticular pathology (e.g., myopathy, rheumatoid arthritis)
* Neurological conditions/cardiovascular events (e.g., stroke, peripheral neuropathy
18 Years
ALL
No
Sponsors
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Unidade Local de Saúde de Coimbra, EPE
OTHER
Responsible Party
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CTU-CACC
Nephrology Nurse Ricardo Ferreira
Principal Investigators
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Ricardo A. S. Ferreira, Bachelor's degree in Nursing
Role: PRINCIPAL_INVESTIGATOR
Unidade Local de Saude de Coimbra
Locations
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Unidade Local de Saude de Coimbra
Coimbra, Coimbra District, Portugal
Countries
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Central Contacts
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Ricardo A. S. Ferreira, Bachelor's degree in Nursing
Role: CONTACT
Clinical Trials Unit Unidade Local de Saude de Coimbra
Role: CONTACT
Facility Contacts
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Clinical Trials Unit Unidade Local de Saude de Coimbra
Role: primary
Other Identifiers
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035 / 24 CE
Identifier Type: -
Identifier Source: org_study_id
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