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Effect of Exercise With Virtual Reality in Hemodialysis Patients

Primary Purpose

Kidney Failure, Chronic

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Exercise with non-immersive virtual reality
Exercise with a static pedal
Sponsored by
Universidad Miguel Hernandez de Elche
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Kidney Failure, Chronic focused on measuring Kidney Failure, Chronic, Inflammation, Functional capacity, Psychological state, Renal Dialysis

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria: - Patients with CKF in a stable clinical situation who have been on HD treatment for at least 3 months. Exclusion criteria: Had a myocardial infarction in the 6 months before the start of the study Suffered unstable angina at rest or during exercise Have cerebrovascular diseases (such as transient ischemia or stroke) Present amputation of lower limbs above the knee without prothesis Present a musculoskeletal or respiratory pathology likely to worsen with exercise Present an inability to carry out functional assessment tests Present visual or cognitive impairments that affect the ability to use the VR equipment or understand the VR exercise

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Intervention Group (IG)

    Control Group (CG)

    Arm Description

    They will perform an intradialysis physical exercise program with non-immersive virtual reality during the first two hours of hemodialysis treatment (n = 40).

    They will exercise with a static pedal during the first two hour of hemodialysis treatment (n = 40).

    Outcomes

    Primary Outcome Measures

    Change of Interleuquine 6 (IL-6) (pg/ml)
    Inflammatoy marker
    Change of Tumoral Necrosis Factor-alpha (TNF-alpha) (pg/ml)
    Inflammatoy marker
    Change of C Reactive Protein (CRP) (mg/L)
    Inflammatoy marker
    Change of Intercellular Adhesion Molecule 1 (ICAM 1) (ng/ml)
    Inflammatoy marker
    Change of Vascular cell adhesion protein 1 (VCAM 1) (ng/ml)
    Inflammatoy marker

    Secondary Outcome Measures

    Assessment of the functional capacity of patients: Short Physical Performance Battery (SPPB)
    Mesure dependency, institutionalization, hospitalization and mortality. Score ranges from 1 to 12 points
    Assessment of the functional capacity of patients: 10 Sit To Stand Test (10 STS).
    Seconds it takes for the patient to get up and sit down 10 times
    Assessment of the functional capacity of patients: 60 Sit To Stand Test (60 STS).
    Number of times the patient gets up and sits down during 60 seconds
    Assessment of the functional capacity of patients: 6 minute walk test (6MWT)
    Meters that a patient is able to walk for 6 minutes
    Psychological assessment of patients: Multidimensional Questionnaire of Adaptation to the Disease for Renal Patients on Dialysis
    It consists of two phases: Phase A and Phase B. The Phase A, which includes 12 items, collects all the information from the clinical history of the patient. This phase includes two areas "Data Doctors" and "Previous Psychopathological History". Phase B, which includes 51 items, it is made up of nine areas that make up the evaluation of the patient. This phase includes the following areas: "Sociodemographic data" (6 items), "Information",(9 items), "Medication and diet" (3 items), "Social support" (4 items), "State of encouragement" (2 items), "Personal resources, coping and resilience" (8 items), "Learning and perceived changes" (5 items), "Spirituality" (2 items) and "Care planning" (2 items). The questions have four formats of response; three of them closed in nature (dichotomous responses, nominal categorical, and 10-point Likert-type scales), and one open and qualitative. An increase in the scale score is positive. A change α < 0.05 is considered statistically significant.

    Full Information

    First Posted
    September 25, 2022
    Last Updated
    February 16, 2023
    Sponsor
    Universidad Miguel Hernandez de Elche
    Collaborators
    European University of Madrid
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05606484
    Brief Title
    Effect of Exercise With Virtual Reality in Hemodialysis Patients
    Official Title
    Effect of Virtual Reality Exercise on Hemodialysis Patients: A Randomized Controlled Clinical Trial Research Protocol
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    June 9, 2023 (Anticipated)
    Primary Completion Date
    October 1, 2023 (Anticipated)
    Study Completion Date
    December 1, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Universidad Miguel Hernandez de Elche
    Collaborators
    European University of Madrid

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Background. An increase in inflammatory biomarkers is associated with impaired kidney function and increased cardiovascular risk and mortality. Physical exercise has been shown to improve the functional capacity and inflammatory status of patients undergoing hemodialysis (HD) treatment, increasing their health-related quality of life. Virtual reality (VR) is an effective and safe tool to increase patient adherence to the exercise program, however, there are very few studies that analyze its effect on the functional capacity of patients with chronic kidney disease (CKD) in HD and none analyze its effect on the inflammatory state of these patients, which justifies the performance of this study. Methods. Eighty patients with CKD on HD treatment will be randomly assigned into two groups, one of them will perform an intradialysis exercise program with non-immersive VR (intervention group; n=40), and the other will exercise with a static pedal (control group; n). =40). The functional capacity of the patients and their inflammatory and psychological status, as well as their exercise adherende, will be analyzed before and after exercise programs.
    Detailed Description
    Description of the intervention The exercise program will last for 12 weeks. Randomly, half of the patients will be instructed to - Control Group (CG): They will be instructed to exercise with a static pedal (control group) and the other half will be instructed to carry out the intradialysis non-immersive virtual reality exercise program. Intervention Group (IG): Will perform an intradialysis physical exercise program with non-immersive virtual reality during the first two hours of hemodialysis treatment (n = 40). Control Group (CG): They will exercise with a static pedal (n = 40). Exercise program The direction and supervision of the exercise programs will be the responsibility of the nursing staff of the Hemodialysis Unit and several physiotherapists of the Rehabilitation Unit of the General University Hospital of Alicante Doctor Balmis, the nursing staff being in charge of directing and supervising the intradialysis exercise program. Prior to the beginning of the intervention, said personnel will receive exhaustive training on the characteristics of the exercise program and on how to carry it out in an optimal way. In this training they will be instructed on how to execute each of the exercises in the program with virtual reality. During the two weeks prior to the intervention, a "first contact" period will be carried out, during which the nursing staff will implement the virtual reality intradialis exercise program as a test, so that they can familiarize themselves with the material necessary to exercise, as well as resolve any doubts that may arise. This trial period will be supervised by the physiotherapist in charge of giving them the training. On the other hand, to improve adherence to exercise by patients and avoid losses throughout the program, all the staff in charge of directing and supervising the exercise will receive a training session by a psychologist specialized in managing barriers in special populations during exercise, with the aim of developing strategies to address these barriers during the intervention period. The exercise program will have a duration of 12 weeks, with a frequency of 3 exercise sessions per week, these being of a progressive duration according to the patient's capacity (EEP 13-15), until reaching 30 minutes per session, and performed during the first two hours of HD treatment. Before and after each exercise session, heart rate and blood pressure will be recorded. Patients will be instructed to perform the exercise independently or with minimal assistance. The non-immersive virtual reality exercise program is described below: - Intervention Group (IG): Participants assigned to this group will start with a 5-minute warm-up session and then perform a virtual reality exercise session for up to a maximum of 30 minutes, depending on the rate of perceived exertion that should be felt between "somewhat hard" and "hard" (13-15 out of 20 in EEP). The intensity will progress by increasing the number of exercise series (each lasting 3 minutes) and may vary between 1 and 10 series, depending on the patient's capacity, taking a 1-minute break between each series. The hemodialysis session may be carried out simultaneously with the exercise, since the work will focus on the lower limbs. An adapted version of ACT (Treasure Hunt) will be used for the VR program. ACT is a non-immersive virtual reality system designed with a playful scheme. For the participants, the system is an intradialysis virtual reality game, which makes dialysis sessions more enjoyable. In ACT, the subject tries to hit a series of targets (avoiding obstacles) by moving the leg. The difficulty in ACT is graduated according to the characteristics of the participants, who will be able to change the leg during the game when they feel tired. The general hardware setup consists of a standard computer, a television (commonly found in HD units), and a Ms Kinect® motion tracking system. At the beginning of the session, the therapists define the VR intervention for the session using a management tool, adding different rest periods and configuring their duration. The difficulty level of the exercise will also be set at startup, and therapists will be able to program the system to automatically increase or decrease the difficulty level depending on the participant's performance. Before their first session, each participant will receive instructions on the general use of the system and a test session will take place. At the end of the program, participants will end the session with another 5 minutes of gentle stretching. Control group (CG): The participants in this group will exercise with a static pedal, exercising the same muscle groups as the VR group. They will perform the exercise at the same time as the VR group, during the first two hours of hemodialysis, with a duration of 30 minutes each session, performing 3 weekly sessions at a perceived exertion intensity of 12-15 (something hard-hard) in the Borg scale. The patients will be blind, being distributed in the hemodialysis room so that in one area there are the patients who exercise with VR and in the other the patients who exercise with a static pedal.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Kidney Failure, Chronic
    Keywords
    Kidney Failure, Chronic, Inflammation, Functional capacity, Psychological state, Renal Dialysis

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Experimental, controlled and randomized study, whose methodology complies with the CONSORT standards for clinical trials
    Masking
    ParticipantOutcomes Assessor
    Masking Description
    The patients and the evaluator will be blind.
    Allocation
    Randomized
    Enrollment
    80 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intervention Group (IG)
    Arm Type
    Experimental
    Arm Description
    They will perform an intradialysis physical exercise program with non-immersive virtual reality during the first two hours of hemodialysis treatment (n = 40).
    Arm Title
    Control Group (CG)
    Arm Type
    Active Comparator
    Arm Description
    They will exercise with a static pedal during the first two hour of hemodialysis treatment (n = 40).
    Intervention Type
    Other
    Intervention Name(s)
    Exercise with non-immersive virtual reality
    Intervention Description
    Patients will exercise for 30 minutes with non-immersive virtual reality (VR) with a perceived exertion between 12-15 (somewhat hard-hard) on the Borg scale. Patients will perform 3 weekly sessions during the second hour of hemodialysis, on simultaneous days.
    Intervention Type
    Other
    Intervention Name(s)
    Exercise with a static pedal
    Intervention Description
    Patients will exercise with a stationary pedal for 30 minutes at an intensity of 12-15 (somewhat hard-hard) on the Borg scale of perceived exertion. The patients will carry out an exercise session 3 times a week on alternate days, coinciding with the patients of the exercise with VR.
    Primary Outcome Measure Information:
    Title
    Change of Interleuquine 6 (IL-6) (pg/ml)
    Description
    Inflammatoy marker
    Time Frame
    Change from Baseline IL-6 at 12 weeks
    Title
    Change of Tumoral Necrosis Factor-alpha (TNF-alpha) (pg/ml)
    Description
    Inflammatoy marker
    Time Frame
    Change from Baseline TNF-a at 12 weeks
    Title
    Change of C Reactive Protein (CRP) (mg/L)
    Description
    Inflammatoy marker
    Time Frame
    Change from Baseline CRP at 12 weeks
    Title
    Change of Intercellular Adhesion Molecule 1 (ICAM 1) (ng/ml)
    Description
    Inflammatoy marker
    Time Frame
    Change from Baseline ICAM 1 at 12 weeks
    Title
    Change of Vascular cell adhesion protein 1 (VCAM 1) (ng/ml)
    Description
    Inflammatoy marker
    Time Frame
    Change from Baseline VCAM 1 at 12 weeks
    Secondary Outcome Measure Information:
    Title
    Assessment of the functional capacity of patients: Short Physical Performance Battery (SPPB)
    Description
    Mesure dependency, institutionalization, hospitalization and mortality. Score ranges from 1 to 12 points
    Time Frame
    baseline and up to 12 weeks
    Title
    Assessment of the functional capacity of patients: 10 Sit To Stand Test (10 STS).
    Description
    Seconds it takes for the patient to get up and sit down 10 times
    Time Frame
    baseline and up to 12 weeks
    Title
    Assessment of the functional capacity of patients: 60 Sit To Stand Test (60 STS).
    Description
    Number of times the patient gets up and sits down during 60 seconds
    Time Frame
    baseline and up to 12 weeks
    Title
    Assessment of the functional capacity of patients: 6 minute walk test (6MWT)
    Description
    Meters that a patient is able to walk for 6 minutes
    Time Frame
    baseline and up to 12 weeks
    Title
    Psychological assessment of patients: Multidimensional Questionnaire of Adaptation to the Disease for Renal Patients on Dialysis
    Description
    It consists of two phases: Phase A and Phase B. The Phase A, which includes 12 items, collects all the information from the clinical history of the patient. This phase includes two areas "Data Doctors" and "Previous Psychopathological History". Phase B, which includes 51 items, it is made up of nine areas that make up the evaluation of the patient. This phase includes the following areas: "Sociodemographic data" (6 items), "Information",(9 items), "Medication and diet" (3 items), "Social support" (4 items), "State of encouragement" (2 items), "Personal resources, coping and resilience" (8 items), "Learning and perceived changes" (5 items), "Spirituality" (2 items) and "Care planning" (2 items). The questions have four formats of response; three of them closed in nature (dichotomous responses, nominal categorical, and 10-point Likert-type scales), and one open and qualitative. An increase in the scale score is positive. A change α < 0.05 is considered statistically significant.
    Time Frame
    baseline and up to 12 weeks

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion criteria: - Patients with CKF in a stable clinical situation who have been on HD treatment for at least 3 months. Exclusion criteria: Had a myocardial infarction in the 6 months before the start of the study Suffered unstable angina at rest or during exercise Have cerebrovascular diseases (such as transient ischemia or stroke) Present amputation of lower limbs above the knee without prothesis Present a musculoskeletal or respiratory pathology likely to worsen with exercise Present an inability to carry out functional assessment tests Present visual or cognitive impairments that affect the ability to use the VR equipment or understand the VR exercise

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Effect of Exercise With Virtual Reality in Hemodialysis Patients

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