Efficacy of an Intradialysis Combined Training Program on Disability Level and Physical Performance.

NCT02883309 · Status: APPROVED_FOR_MARKETING · Type: EXPANDED_ACCESS

Last updated 2016-09-30

No results posted yet for this study

Summary

The patient subjected to hemodialysis has a low physical capacity due to being advanced in years and the complexity of the process, which is encouraged by family members and caregivers who lead them to a total dependence. The Intradialytic physical exercise is presented as an alternative to counteract this functional deterioration of patients with terminal chronic kidney failure.

Conditions

  • Chronic Renal Failure

Interventions

OTHER

intradialytic physical training program

Nine patients participated in the experimental group in a combined training program, which lasted 12 weeks with a frequency of 3 times a week, the training sessions were carried out within each dialysis session during the first 2 hours of the dialysis treatment, the working session involved a warm up period, aerobic exercise with pedals, or strength exercises based on free weight depending on the training stage. The Borg scale and the heart rate reserve were used to control the training intensity. The disability level was evaluated at the beginning and the end of the study through the World Health Organization Disability Assessment Schedule II, the aerobic capacity was evaluated through the six minute walk and the limbs strength was evaluated through a dynamometer.

Sponsors & Collaborators

  • Nephrocare Portugal

    collaborator INDUSTRY
  • Universidad Austral de Chile

    lead OTHER

Principal Investigators

  • Paula I Moscoso, Mph PTh · Universidad Austral de Chile

  • Roberto G Mancilla, Student · Universidad Austral de Chile

  • Cesar E Gonzalez, Student · Universidad Austral de Chile

  • Manuel Monrroy, Msc(c) PTh · Universidad Austral de Chile

  • Lizzy Orellana, MD · Universidad Austral de Chile

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2014-01-31
Completion
2014-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02883309 on ClinicalTrials.gov