Skip to main content
OpenTrials
Completed

NCT Number: NCT02834026

Impact of the Cycle Ergometer in Muscle Strength and Pulmonary Function in Patients in Hemodialysis

Muscle strength can be measured by dynamometry, but the investigators did not find in the literature the study of this technique in the quadriceps of patients with chronic kidney disease on hemodialysis. Analyze training impact conducted by cycle ergometer in quadriceps muscle strength in patients with chronic kidney disease during hemodialysis. This study will be a prospective, randomized. Inclusion of 46 patients followed by the dialysis unit of a university hospital, over 18 years, of both genders who underwent hemodialysis for more than six months and signed the consent form and enlightened. Patients will be divided into two groups: Intervention (n = 23) and control (n = 23). All will be evaluated for demographics and quadriceps strength given by standardization of technique, with hard and windy belt. The control group will be reassessed after two months of the initial assessment, since the intervention group held two months of training in hemodialysis a physical therapy protocol with the cycle ergometer.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Chronic Renal Disease Behavior Chronic Disease Disease Attributes Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Kidney Diseases Male Urogenital Diseases Motor Activity Pathologic Processes Pathological Conditions, Signs and Symptoms Renal Dialysis Renal Insufficiency Renal Insufficiency, Chronic Urogenital Diseases Urologic Diseases

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Vera Lúcia dos Santos Alves

São Paulo, Brazil

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged over 18 years
  • Performing HD over six months
  • Clinically stable
  • Patients no diagnosis of lung disease
  • Neurological or mioarticular previous or current and agreed to participate in the study and signed informed consent and informed

Exclusion criteria

  • Patients undergoing elective surgery or emergency six months before or during the performance of the protocol
  • Cardiac decompensation
  • Used continuous or nocturnal oxygen
  • Patients using bracing of the lower limbs.

Treatment and study plan

Cicloergometry training

Other

No Cicloergometry training

Other

Primary outcomes

  1. Muscle strength evaluated by dynamometry

    Time frame: Two months

    dynamometry

  2. Peripheral blood tests

    Time frame: Two months

    hemoglobin (g / dL)

  3. Peripheral blood tests

    Time frame: Two months

    serum albumin (GDL)

  4. Peripheral blood tests

    Time frame: Two months

    Creatinine (mg / dL)

  5. Peripheral blood tests

    Time frame: Two months

    Urea (mg / dL)

  6. Peripheral blood tests

    Time frame: Two months

    Kt / V

Sponsors and collaborators

Lead sponsor

Faculdade de Ciências Médicas da Santa Casa de São Paulo

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2018
First posted
Jul 15, 2016
Registry last updated
Dec 2, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.