Effect of Autogenic Training on Hemodialysis Patients (NCT07276828) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Autogenic Training on Hemodialysis Patients
Egypt54 participantsStarted 2025-12-15
Plain-language summary
goal of this interventional study to investigate the effect of autogenic training on sleep disturbance , restless leg syndrome and fatigue on hemodialysis patient Is there any significant effect of autogenic training on restless leg syndrome, sleep disturbance and fatigue in patients with hemodialysis?
The intervention will include structured autogenic training sessions, and outcomes such as sleep quality and RLS severity and fatigue will be evaluated after 8 weeks of autogenic training on hemodialysis patients .
Who can participate
Age range
45 Years – 55 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria
* Age between 45 and 55 years.
* Body Mass Index (BMI) between 25.0 and 29.9 kg/m².
* Clinically and medically stable.
* On hemodialysis for at least 6 months prior to enrollment.
* Diagnosed with chronic kidney disease (CKD), defined by one or more of the following:
Evidence of kidney damage (e.g., albuminuria), or
Decreased kidney function with glomerular filtration rate (GFR) \< 60 mL/min/1.73 m² for ≥ 3 months, irrespective of clinical diagnosis.
\*Systolic blood pressure \< 140 mmHg, diastolic blood pressure \< 90 mmHg, and heart rate \< 80 bpm.
Exclusion Criteria
Uncontrolled pulmonary disease.
Severe vascular complications (e.g., critical limb ischemia).
Unstable angina.
Uncontrolled cardiac arrhythmia.
Decompensated heart failure.
Cognitive impairment.
Participants who miss more than two weeks of the program or request termination.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.