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Investigating the Effect of Tai Chi in Hemodialysis Patients

Investigating the Effect of Tai Chi Exercises on Sleep Quality, Fatigue Levels, and Selected Physiological Parameters in Patients with Chronic Kidney Disease Undergoing Hemodialysisfvv

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20260314068987N1
Enrollment
82
Registered
2026-04-18
Start date
2026-04-04
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

Chronic kidney disease. Chronic kidney disease (CKD)

Interventions

Intervention 1: "Intervention group: For 12 weeks, participants will engage in Tai Chi protocol (10 standard forms of Yang style Tai Chi Chuan) for 3 sessions per week, each lasting 40-60 minutes. Thi
however, at the end of the study, they will be provided with the training materials and videos prepared for the intervention group.".

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Willingness and Consent to Participate in the Study A minimum of 3 months of hemodialysis history Confirmation by a nephrologist for the patient’s participation in the study Ability to perform gentle physical movements Absence of acute illnesses Not receiving other exercise interventions PSQI score > 5 Possession of a smartphone Access to the internet Being literate

Exclusion criteria

Exclusion criteria: The existence of underlying disease Severe mobility limitations Age less than 18 years

Design outcomes

Primary

MeasureTime frame
Sleep Quality. Timepoint: Before the start of the study, time point zero immediately after the intervention and 1 month after the end of the study. Method of measurement: Pittsburgh Sleep Quality Index (PSQI) questionnaire.;Fatigue Levels. Timepoint: Before the start of the study, time point zero immediately after the intervention and 1 month after the end of the study. Method of measurement: Multidimensional Fatigue Inventory (MFI) questionnaire.;Dialysis adequacy. Timepoint: Before the start of the study, time point zero immediately after the intervention and 1 month after the end of the study. Method of measurement: It will be calculated by the researcher using the standard Kt/V formula based on information collected from patient records.;Systolic and diastolic blood pressure. Timepoint: Before starting the study at time point zero, immediately after the intervention, and one month after the study completion. Method of measurement: Blood pressure data (systolic and diastolic) will be measured according to standard guidelines from the American Heart Association using a standard mercury sphygmomanometer and a calibrated digital sphygmomanometer with an appropriate cuff.;Blood urea nitrogen (BUN) and serum creatinine levels. Timepoint: Before starting the study at time point zero, immediately after the intervention, and one month after the study completion. Method of measurement: Data on blood urea nitrogen (BUN) and serum creatinine levels will be extracted from routine monthly biochemical tests recorded in the medical records of hemodialysis patients at the dialysis center of Boali Sina Hospital, Qazvin.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Ahmadvand

Qazvin University of Medical Sciences

Azadeh.ahmadvand@yahoo.com+98 28 3333 9537

Outcome results

None listed

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