Actively Recruiting
Physical Impairments in Children With Chronic Renal Failure
Led by Izmir Democracy University · Updated on 2025-08-28
25
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
When the literature is examined, it is seen that the extent to which cough strength, grip strength, physical activity level and quality of life levels are affected in children with chronic kidney failure compared to healthy children is not sufficiently clarified. For this reason, this study aimed to reveal impairments in grip strength, cough strength, physical activity, sleep quality or quality of life in children with chronic renal failure compared to healthy children.
CONDITIONS
Official Title
Physical Impairments in Children With Chronic Renal Failure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children and adolescents aged 8 to 18 years with chronic kidney failure
- Clinically stable for at least the last 3 weeks (for those with chronic kidney failure)
- Able to cooperate with the measurements
- Willing to participate in the study
- Healthy children and adolescents aged 8 to 18 years
- Able to cooperate with the measurements
- Willing to participate in the research
You will not qualify if you...
- History of orthopedic, neurological, cardiovascular, or psychological problems preventing measurements in the last 6 months (for chronic kidney failure group)
- Smoker or former smoker
- Having had a kidney transplant (for chronic kidney failure group)
- History of orthopedic, neurological, cardiovascular, or psychological problems preventing measurements in the last 6 months (for healthy group)
- Having any chronic disease (for healthy group)
- Smoker or former smoker
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
İzmir Demokrasi Üniversitesi
Izmir, Turkey (Türkiye), 35140
Actively Recruiting
Research Team
G
Gülşah Barğı
CONTACT
H
Hüseyin Kıran
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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