The Effect of Nutrition Education Hemodialysis Patients

NCT ID: NCT06217692

Last Updated: 2024-01-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-12-15

Study Completion Date

2024-08-02

Brief Summary

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type of study: Clinical trial Purpose of the study: The aim of this study was to investigate the effect of nutrition education on dietary attitudes and daily consumption of essential nutrients in patients receiving haemodialysis treatment.

Detailed Description

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Patients who agree to participate in the study will be included in the experimental group and control group as a result of statistical analysis and the number of patients will be determined. Then, the patients will be assigned to the groups with the randomisation method of;simple and stratified sampling;. The experimental and control groups within the scope of the research will be determined by simple randomisation method (coin toss). In the first interview, the individuals in the training group will be administered the Individual Information Form; and the;Attitude Scale of Hemodialysis Patients towards Diet Therapy as a pre-test by the researcher using the face-to-face interview method. Then, 24-Hour Food Consumption Record will be given and all food/liquids eaten and drunk for 24 hours retrospectively will be asked to be written on this form. At this stage, the researchers will help the participants to fill in the food consumption record if needed. This process will take approximately 20 minutes and the food consumption record will be collected again. Then, the individuals in the training group will be informed about nutrition education and the first nutrition education will be started. The training will last for 4 weeks, twice a week, and the length of the training will be forty minutes. After the last of the trainings, which will last 8 times in total, the Attitude Scale of Hemodialysis Patients towards Diet Therapy will be applied as a post-test using the face-to-face interview method. In the same way, 24-Hour Food Consumption Record will be given and all food/liquids eaten and drunk for 24 hours retrospectively will be asked to be written on this form. In the control group, pretest data forms (Individual Information Form and Attitude Scale towards Diet Therapy of Haemodialysis Patients) and three-day 24-Hour Food Consumption Record will be filled out, and the Attitude Scale and three-day 24-Hour Food Consumption Record will be filled out one month later as the posttest.

Conditions

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Haemodialysis Patients

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants

Study Groups

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experimental group

experimental group

Group Type EXPERIMENTAL

nutrition education

Intervention Type OTHER

nutrition education

control group

control group

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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nutrition education

nutrition education

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* \- Receiving treatment in the haemodialysis unit of Bayburt State Hospital, having contact addresses in electronic media,
* Maintaining haemodialysis treatment for the last 3 months
* No significant psycho-emotional problems,
* It will consist of patients who are not taking any psychotropic medication and who volunteer to participate in the study.

Exclusion Criteria

* \- Reluctance to continue co-operation,
* Moving from the haemodialysis centre to other centres for any reason,
* The emergence of acute and malignant disease,
* The need for transplantation for any reason
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bayburt University

OTHER

Sponsor Role lead

Responsible Party

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Zahide Akeren

Director

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Bayburt University

Bayburt, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Researcher

Identifier Type: OTHER

Identifier Source: secondary_id

Researcher

Identifier Type: -

Identifier Source: org_study_id

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