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Published on: March 29, 2019
Intradialytic resistance training: an effective and easy-to-execute strategy
Antônio Paulo André de Castro1, Sergio Ribeiro Barbosa2, Henrique Novais Mansur3
1Programa de Pós-graduação em Saúde, Faculdade de Medicina, Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brasil.
Intradialytic resistance training (IRT) significantly improves physical capacity and quality of life in chronic kidney disease patients undergoing hemodialysis. This safe and effective low-cost protocol enhances muscle strength and walking speed, benefiting patient well-being.
Area of Science:
- Nephrology
- Exercise Physiology
- Rehabilitation Medicine
Background:
- Chronic kidney disease (CKD) impairs skeletal muscle function, reducing physical capacity (PC) and quality of life (QoL) in patients.
- Intradialytic resistance training (IRT) is a potential intervention to mitigate these effects but lacks widespread adoption.
Purpose of the Study:
- To evaluate the efficacy and safety of a low-cost, user-friendly IRT protocol for CKD patients on hemodialysis.
- To assess improvements in physical capacity (PC) and quality of life (QoL) following IRT.
Main Methods:
- 43 hemodialysis patients (mean age 52.8 years) participated in a 9.3-month study.
- An intradialytic resistance training (IRT) protocol involving moderate-to-high intensity exercises for major muscle groups was implemented three times weekly.
- Efficacy was measured by changes in muscle strength (MS) and preferred walking speed (PWS); safety was monitored via adverse events.
Main Results:
- High compliance (96.5%) with the IRT protocol was observed.
- Significant improvements were noted in muscle strength (27.3 to 34.8 Kgf) and preferred walking speed (0.99 to 1.26 m/s).
- Both physical and emotional aspects of quality of life (QoL) showed significant increases.
Conclusions:
- Intradialytic resistance training (IRT) effectively enhances physical capacity (PC) and quality of life (QoL) in CKD patients.
- The implemented IRT protocol was safe, with no major adverse events reported.
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