The effects of appropriate nutrition education in small groups on the laboratory values in the hemodialysis patients

Not Applicable

• Conditions: N18, N19; Chronic Renal Failuer Patients who need hemodialysis.

• Registration Number: IRCT2016082229481N1
• Lead Sponsor: Zanjan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

Criteria for study:
1. age 18 to 70 years
2. No known psychiatric disorders and psychiatric treatment, according to a Psychiatrist Specializing
3. The absence of any cognitive impairment, speech or hearing
4. The lack of pain during training
5. dialysis in Zanjan
6. phone access
7. having full consent to participate in the study
8. The End-Stage Renal Disease that is constantly undergoing Hemodialysis program
9. two to three times a week for three to four hours is treated with dialysis
10. Having read and write at least
11. sick or disabled family members are able to understand and speak the Persian orTurkish or Azari language
12. caregivers of patients who have the greatest participation in the treatment of disease, and he spent the most time with and least education (literacy), respectively.
Exclusion criteria:
1. Used to treat kidney transplant during the study
2. migration from dialysis during the study
3. patient died during the study
4. who frequently ill during hemodialysis and hemodialysis have not been able to afford full-time
5. The incidence of severe deterioration and the development of critical situations for each of the samples during the study
6. Not wanting to take part in a training session or a follow-up sessions during the study

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The laboratory values BUN,Cr, Na, K, Ca, P. Timepoint: wo months before and two months after intervention. Method of measurement: five ml blood samples from patients and Biochemical reagents Company Bayvrks England.