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EXerCise Introduction To Enhance Performance in Dialysis(EXCITE)

EXerCise Introduction To Enhance Performance in Dialysis: the EXCITE Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01255969
Acronym
EXCITE
Enrollment
500
Registered
2010-12-08
Start date
2010-04-30
Completion date
2015-07-31
Last updated
2016-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients on Dialysis (Hemodialysis, Peritoneal Dialysis)

Keywords

Dialysis, Physical exercise, Clinical Trial, Quality of Life, Performance, Fitness, Cardiovascular Mortality, Vascular access

Brief summary

To evaluate if a model of intervention based on a low-grade physical program prescribed in the dialysis centre and performed at home can modify the functional capacity and quality of life, reduce the risk of cardiovascular and all-causes mortality, non-fatal cardiovascular events and vascular access failure in dialysis patients.

Detailed description

Background Dialysis patients show an exceedingly higher risk of death and cardiovascular complications (1). These patients are also characterized by poor physical performance and reduced quality of life. Observational findings in the United States Renal Data System (USRDS) indicated that physical rehabilitation programs after coronary artery bypass are associated with better clinical outcomes in this population (2). However, the hypothesis that physical training in dialysis patients may translate into better physical performance and clinical outcomes has never been tested in large randomized clinical trials. In studies performed so far, physical exercise was proposed during the dialysis session or between two dialysis sessions. These programs imply compliance, organization and cost problems, mainly related with intensification of visit to the dialysis centre. To limit these difficulties, a single easy-to-implement program of physical exercise for dialysis patients, prescribed in the dialysis centre but performed at home, has been recently elaborated and a pilot study has shown that this program improves physical performance in medium term (3). Purpose This clinical trial tests whether a physical program prescribed in the dialysis centre but performed at home improves the degree of fitness and the quality of life in dialysis patients. Study population * Inclusion Criteria: * 500 Patients on dialysis * Dialysis vintage\>6 months * Age\>18 years * Signed informed consent * Stable clinical conditions * Exclusion Criteria: * physical or clinical limitations to deambulation Outcomes: * Functional capacity : Evaluation of the variation in the distance covered in a pre-determined time with a validated walking test (six minute walking test); Evaluation of the variation in the time needed to complete 5 cycles of the sit-to-stand-to sit test. * Quality of Life : Score obtained by a validated questionnaire for dialysis patients (Kidney Disease Quality of Life instrument o KDQOL). * Fatal and non-fatal events (cardiovascular and all-causes). * All-cause hospitalizations. * Vascular access survival. The power analysis was performed by calculating the sample size for each clinical outcome contemplated by the study protocol. The overall sample size of the trial is that portended by the calculation demanding the highest individuals numbers (that of the outcome fatal and non fatal cardiovascular events in our instance). In a previous observational study by our group, the incident rate of fatal and non fatal cardiovascular events was at three years 25% (4). We hypothesised that the physical exercise will produce a 10% reduction in the hazard ratio of fatal cardiovascular events (hazard ratio: 0.70) as compared to that of the control group. References: 1. Mallamaci F, Tripepi G, Cutrupi S, Malatino LS, Zoccali C. Prognostic value of combined use of biomarkers of inflammation, endothelial dysfunction, and myocardiopathy in patients with ESRD. Kidney Int. 2005 Jun;67(6):2330-7. PMID: 15882276 2. Kutner NG, Zhang R, Huang Y, Herzog CA. Cardiac rehabilitation and survival of dialysis patients after coronary bypass. J Am Soc Nephrol. 2006 Apr;17(4):1175-80. Epub 2006 Feb 15. PMID: 16481413 3. Malagoni AM, Catizone L, Mandini S, Soffritti S, Manfredini R, Boari B, Russo G, Basaglia N, Zamboni P, Manfredini F. Acute and long-term effects of an exercise program for dialysis patients prescribed in hospital and performed at home. J Nephrol. 2008 Nov-Dec;21(6):871-8. PMID: 19034871 4. Zoccali C, Tripepi G, Mallamaci F.Predictors of cardiovascular death in ESRD.Semin Nephrol. 2005 Nov;25(6):358-62

Interventions

OTHERExercise

Personalized exercise program

Sponsors

Fondazione C.N.R./Regione Toscana G. Monasterio, Pisa, Italy
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients on dialysis * Dialysis vintage\>6 mo. * Age\>18 aa. * Signed informed consent * Stable clinical conditions

Exclusion criteria

-any physical or clinical limitations to deambulation

Design outcomes

Primary

MeasureTime frameDescription
Assessment of Quality of Life (QoL) modification by the KIDNEY DISEASE QUALITY OF LIFE (KDQOL)questionary6 months6 months is the time frame for the primary analysis but the follow-up will continue until 3 years.
Assessment of functional capacity by Six-Minute Walking test and Sit-to-Stand-to-sit test6 months6 months is the time frame for the primary analysis but the follow-up will continue until 3 years.

Secondary

MeasureTime frameDescription
Evaluation of mortality (all causes and cardiovascular only), non-fatal cardiovascular events, all-causes hospitalizations and dialysis access survival.6 months6 months is the time frame for the primary analysis but the follow-up will continue until 3 years.
All - causes and cardiovascular hospitalizations6 monthsHospitalizations will be characterized by ICD-9 codes. Six months is the time frame for the primary analysis but the follow-up will continue until 3 years.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026