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Effect of a course of aerobic training versus control group on blood factors and psychological symptoms in patients undergoing hemodialysis

Effect of a course of aerobic training versus control group on blood factors and psychological symptoms in patients undergoing hemodialysis: a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120215009014N608
Enrollment
40
Registered
2026-05-14
Start date
2026-05-31
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Hemodialysis. Encounter for adequacy testing for hemodialysis

Interventions

Intervention 1: Intervention group: Treatment and routine care for hemodialysis patients, along with aerobic exercises including pedaling on a stationary mini electric bike for 30 minutes, and resista

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age of 18 to 65 years, Patients undergoing hemodialysis,

Exclusion criteria

Exclusion criteria: Movement disorders

Design outcomes

Primary

MeasureTime frame
Blood calcium level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood phosphorus level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood sodium level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood potassium level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood hemoglobin level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood hematocrit level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood platelet level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood creatinine level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood urea level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood albumin level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood triglyceride level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood cholesterol level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood alkaline phosphatase level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood sample.;Blood SGOT level. Timepoint: Before the intervention and three months later. Method of measurement: By taking and testing a blood samp

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFahimeh Ghodrati

Islamic Azad University

fahimeghoratii@gmail.com+98 66 4251 8000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026