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Effects of Resistance Training on Physical Activity in Daily Life and Functional Capacity in Hemodialysis Patients

Not Applicable
Conditions
Renal Insufficiency, Chronic
Interventions
Other: Resistance Exercise Program
Registration Number
NCT02651025
Lead Sponsor
Federal University of Juiz de Fora
Brief Summary

The purpose of this study is to determine whether a supervised resistance exercise training during hemodialysis is effective to increase physical activity in daily life in patients with end stage renal disease.

Detailed Description

The patients will be randomized into two groups: intervention and control groups. Patients in the intervention group will receive a supervised resistance exercise training, during hemodialysis, three times/week for 12 weeks, and patients allocate to the control group will received a passive stretching program during the same timeframe.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
29
Inclusion Criteria
  • Patients with end stage renal disease on hemodialysis for at least three months
  • Sedentary for at least six months
Exclusion Criteria
  • Presence of physical limitations that prevent the implementation of physical tests
  • Presence of severe comorbidity and unstable (unstable angina, decompensated heart failure, myocardial infarction history of the past six months, cardiac arrhythmias, uncontrolled hypertension with systolic blood pressure ≥ 200 mmHg and / or diastolic blood pressure ≥ 120 mmHg, diabetes decompensated, severe lung disease, acute systemic infection as well as neurological disorders, musculoskeletal and osteoarticular or other disabling conditions according to the clinical judgment)
  • Hospitalization in the three months prior to study entry

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Resistance Exercise ProgramResistance Exercise ProgramPatients included in intervention group will submit to resistance exercise training during hemodialysis, three times a week, for twelve weeks. This program includes exercises for the upper and lower limbs.
Primary Outcome Measures
NameTimeMethod
Physical Activity in Daily Life12 weeks

The physical activity in daily life will be estimated as the mean number of steps using a triaxial accelerometer.

Secondary Outcome Measures
NameTimeMethod
Muscle function12 weeks

The muscle function will be assessed by electromyography.

Muscle strength12 weeks

The measurement of maximal voluntary strength of handgrip will be assessed by hydraulic model of dynamometer.

Functional capacity12 weeks

The functional capacity will be assessed by six-minute walking test.

Depression and anxiety12 weeks

Depression and anxiety will be assessed by the Hospital Anxiety and Depression Scale.

Quality of life12 weeks

The quality of life will be assessed by the 36-Item Short Form Health Survey (SF36).

Trial Locations

Locations (1)

University Hospital of the Federal University of Juiz de Fora

🇧🇷

Juiz de Fora, Minas Gerais, Brazil

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