- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02860312
Long Term Physical Activity for Hemodialysis Patients
Effects of One Year Perdialytic Physical Activity on Aerobic Capacities and Quality of Life in Hemodialysis Patients
Patients on chronic hemodialysis present severe physical dysfunctioning associated with a significant reduction of their muscle mass. These two parameters are associated with increased morbidity and mortality along with deconditioning and poor quality of life. There are several studies- usually short term, single center uncontrolled and underpowered- that have shown a significant improvement of the physical, metabolic and dialytic parameters.
There are only few studies that have measured the impact of a long term intradialytic exercise intervention on a supervised manner. This is a multi-center controlled study examining the effects of intradialytic cycling on parameters of physical functioning, body composition, cardiovascular and nutritional status, immunological status and quality of life in a group of clinically stable hemodialysis patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
General Context Chronic Kidney Patients (CKD) live a sedentary life. Sedentarity and Sarcopenia worsen during the evolution of CKD with numerous cardiovascular diseases, infectious and other comorbidities. Inactivity may activate and amplify the inflammatory process, hypercoagulability, malnutrition, invoking a vicious circle of further inactivity and deconditioning.
These populations have a very low physical activity profile due to important tiredness, perturbed general condition and bad adaptation in effort. The patients with cardiovascular problems have additional limitations due to breathlessness associated with congestive cardiac failure and intermittent claudication due to peripheral arteriopathy. At the dialysis stages the tiredness is accentuated after the hemodialysis sessions. The days off dialysis are rarely used for practicing a physical activity.
The deconditioning along with the reduction of the physical activity are leading to a de-socializing progressing in the course of the chronic renal failure. In that way the patient feels more and more isolated with a serious eventual impact on the nutrition status and his quality of life.
Regular physical activity in this population of patients is exerting beneficial effects on insulin resistance, inflammation, dialysis efficiency, nutrition and arterial pressure. It may also reduce the intradialytic hypotensive episodes and improve quality of life, without side effects.
The objective of this study is to investigate an improvement of the physical functioning associated with a reprogramming of the autonomous nervous system, a reduction of the pro-inflammatory factors with a reduction of the insulin resistance (reduction of the metabolic syndrome), along with improvements on the immune system functioning for hemodialysis patients participating on a one year intradialytic physical activity program.
Principal objective :
The principal aim of the present study is to show the efficacy of intradialytic physical activity on functional capacity with the sit-to-stand test in 60 seconds (STS60) and the time to perform 5 complete sit-to-stand movements (STS5) along with a 6 minutes' walk test (6MWT).
Secondary objectives :
The secondary objectives are the amelioration of parameters associated with cardiovascular, sympathetic or autonomous nervous system, immune, nutritional, metabolic and inflammatory outcomes among with quality of life.
This is a multicenter, controlled randomized trial
Study description:
Inclusion of patients willing to participate in the study, and consequently their randomization in 2 groups.
The intervention group will benefit from a supervised physical activity during the dialysis session and the other group will carry on with his usual physical activities and have the same tests before and after the trial without undergoing a supervised intradialytic physical activity program
Primary judgment criteria :
The principal criteria will be the effect of an aerobic training program with a warming up phase, followed by 30 minutes of intradialytic cycling on 55% of the VO2max, 3 times a week.
The primary judgement criteria will be the improvement of the Sit-to-stand test in 60 seconds (STS60) and the time to complete 5 sit-to stand movements (STS5) as well as the 6 minutes' walk test (6MWT) from T0 (before the training program) to T12 (12 months after the start of the training period)
Secondary criteria:
- Quality of life parameters evaluated from the questionaries SF36 (The Short Form (36) Health Survey), Borg scale, EVA.
- Physical activity levels: IPAQ (international physical activity questionary).
- Body composition (Fat mass, lean mass, bone mineral density, estimation of the muscular mass) with DEXA (dual-energy x-ray absorptiometry).
- Cardiovascular parameters : Cardiac echography, doppler of the carotid arteries and the lower extremity arteries, 24h cardiac rhythm exploration
- Immune parameters: leucocyte subpopulation functioning
- Nutritional and metabolic parameters: weight, BMI, albumin, pre-albumin, pre- and post-dialytic serum urea and creatinine levels, nPCR (normalised Protein catabolic Rate).
- Inflammatory parameters :(Interleucin) IL1 bêta, IL6, IL8, IL-10, TNF alpha (Tumor necrosis factor alpha), CRP (C reactive protein)
- Dialysis parameters : Kt/v, anemia control : Hemoglobin (Hb), MCV (mean corpuscular volume), ferritin, erythropoetin dosage (EPO).
- Number, etiology and duration of hospitalisations
- Survival in 1 year
Number of participants : 100, ie 50 per group
Layout of the study :
Inclusion of the patient, evaluations at the start of the study protocol, at 6 months and at the end -12 months (M0, M6, M12).
Benefits and risks of this study :
Improvement of functional aerobic capacity, inflammatory status and quality of life. Improvements on the state of pain, autonomy, augmentation of the lean mass with conservation of the muscular mass for the lower extremities and reduction of the total fat mass are expected as well as improvement of the nutritional status, dialysis parameters, anemia control.
The risks are of cardiovascular origin: a possible decompensation of coronary artery disease, peripheral artery disease, taking into consideration that all patients benefit from echo doppler arterial control before the start of the study.
Regular Perdialytic Activity during Dialysis is practiced in AURA Auvergne (Association pour l'Utilisation du Rein Artificiel Santé) since 2 years; there has been no secondary vascular problem associated with the supervised physical activity. Nevertheless, rare tendon problems or articular and muscular pains could be possible on the course of the study
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Consenting active hemodialysis patients since at least 6 months aged between 20 and 90 y.o.
Exclusion Criteria:
- Unstable angina,
- severe left ventricular dysfunction,
- Ejection fraction < 30%,
- severe peripheral arterial disease,
- lower extremity amputation,
- impossibility of physical effort: pain, uncontrolled bone/muscular disease,
- participation on another study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
ACTIVE_COMPARATOR: Exercisers
Intradialytic exercise on stationary bicycles
|
Patients are exercising for 30-60 min during dialysis on an Rated Perceived Exertion (RPE) Scale between 12 and 14
|
|
PLACEBO_COMPARATOR: Non Exercisers
No intradialytic exercise
|
Patients are having their usual physical activity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improvement of the distance covered after walking for 6 minutes (6 minutes walk test)
Time Frame: 12 months
|
The principal aim of the present study is to show the efficacy of intradialytic physical activity on the improvement of the physical capacity of the patients assessed with the 6 minutes walk test ((6MWT)
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of life parameters 1
Time Frame: 12 months
|
Quality of life parameters evaluated from the questionnaire SF36 QD
|
12 months
|
|
Quality of life parameters 2
Time Frame: 12 months
|
Quality of life parameters evaluated from the questionnaire Borg scale
|
12 months
|
|
Quality of life parameters 3
Time Frame: 12 months
|
Quality of life parameters evaluated from the EVA scale
|
12 months
|
|
Physical activity levels
Time Frame: 12 months
|
Physical activity levels from the questionnary IPAQ (international physical activity questionnairy)
|
12 months
|
|
Body composition
Time Frame: 12 months
|
Body composition (Fat mass, lean mass, bone mineral density, estimation of the muscular mass) with DEXA ccanning and bioimpendance
|
12 months
|
|
Cardiovascular parameters
Time Frame: 12 months
|
Cardiovascular parameters : Cardiac echography, echodoppler of the carotid arteries and the lower extremity arteries, 24h cardiac rythm exploration
|
12 months
|
|
Immune parametres
Time Frame: 12 months
|
Immune parametres: leucocyte subpopulation fonctioning
|
12 months
|
|
Nutritional and metabolic parameters 1
Time Frame: 12 months
|
BMI
|
12 months
|
|
Nutritional and metabolic parameters 2
Time Frame: 12 months
|
serum albumin levels
|
12 months
|
|
Nutritional and metabolic parameters 3
Time Frame: 12 months
|
serum prealbumin levels
|
12 months
|
|
Nutritional and metabolic parameters 4
Time Frame: 12 months
|
pre and post dialytic serum urea levels
|
12 months
|
|
Nutritional and metabolic parameters 5
Time Frame: 12 months
|
pre and post dialytic serum creatinine levels
|
12 months
|
|
Nutritional and metabolic parameters 6
Time Frame: 12 months
|
nPCR (normalised Protein Catabolic Rate)
|
12 months
|
|
inflammatory parameters 1
Time Frame: 12 months
|
IL1 bêta
|
12 months
|
|
inflammatory parameters 2
Time Frame: 12 months
|
IL6
|
12 months
|
|
inflammatory parameters 3
Time Frame: 12 months
|
IL8
|
12 months
|
|
inflammatory parameters 4
Time Frame: 12 months
|
IL-10
|
12 months
|
|
inflammatory parameters 5
Time Frame: 12 months
|
TNF alpha
|
12 months
|
|
inflammatory parameters 6
Time Frame: 12 months
|
CRP
|
12 months
|
|
Dialysis parameters
Time Frame: 12 months
|
Kt/V
|
12 months
|
|
Anemia control 1
Time Frame: 12 months
|
Hemoglobin (Hb)
|
12 months
|
|
Anemia control 2
Time Frame: 12 months
|
MCV (mean corpuscular volume)
|
12 months
|
|
Anemia control 3
Time Frame: 12 months
|
Ferritine
|
12 months
|
|
Anemia control 4
Time Frame: 12 months
|
Erythropoetine dosage (EPO).
|
12 months
|
|
Number of hospitalisations
Time Frame: 12 months
|
Number of hospitalisations
|
12 months
|
|
Duration of hospitalisations
Time Frame: 12 months
|
Duration of hospitalisations
|
12 months
|
|
Survival
Time Frame: 12 months
|
Survival in one year
|
12 months
|
|
Improvement of Sit to Stand test in 60 seconds (STS60)
Time Frame: 12 months
|
The physical capacity of the patients assessed with the number of cycles performed during a sit-to-stand test in 60 seconds (STS60).
|
12 months
|
|
Improvement of the time needed to perform 5 Sit to Stand cycles (STS5)
Time Frame: 12 months
|
Time needed to perform 5 Sit to Stand cycles (STS5)
|
12 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AURAS
- ID-RCB 2015-A0031-48 (OTHER: CPP Clermont Ferrand)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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