Malnutrition Clinical Trial
Official title:
The Influence of Dietary Phosphorus Education Program on Nutritional Status and Serum Phosphate Level Among Hemodialysis Patient
Aim:
Dietary Phosphorus Education Program can improve patients' knowledge, attitude and behavior
of phosphorus restriction diet to reduce the risk of hyperphosphatemia and malnutrition of
hemodialysis patients.
Inclusion criteria:
The criteria of subjects are undergoing regular hemodialysis for longer than 3 months at
baseline. Subjects' age range is from 20 to 85 years old. Their baseline serum albumin < 4.0
mg/dL, or serum phosphate > 5.0 mg/dL, are eligible for inclusion.
Subjects will be enrolled into this trial after signed informed consent. We expect to recruit
60 subjects. Patients will be excluded if they had liver cirrhosis, malignant tumor, can't
finish all education sessions and/or can't complete dietary records monthly. We will recruit
a control group into this trial, they are eligible for inclusion but don't want to
participant education sessions.
Intervention protocol:
At baseline, the investigators collect demography and pre-test KAP questionnaires among all
subjects. If subjects were illiterate then investigator will conduct face-to-face interview
and record their answers. Dietary Phosphorus Education is a 6-month program and be
implemented by dietitians and investigators, including education, nutritional counseling and
dietary records monthly.
The first month was intensive weekly education sessions, each 20 to 30 minutes. Second and
third month were monthly education sessions, each 20 to 30 minutes. There are total 6
sessions in this trial. The last 3 months will follow-up periods, will collect anthropometry
data monthly, biochemistry measurements and 3-day dietary records among all subjects. If
subjects were illiterate then investigator will conduct face-to-face interview or
phone-interview to complete each dietary record. Investigator collect post-test KAP
questionnaires, diet behavior questionnaires and satisfaction questionnaires from subjects in
the end of the trial,. If subjects are illiterate then investigators interview subjects and
record.
This is a 6-months trial and retrospective study to collect anthropometry, biochemical
measurements and 3-day dietary records from control subjects monthly.
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