Impact of an Intervention Education Program on the Knowledge, Attitudes, and Practices of Dietitians

ConditionNo Conditions
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorUniversiti Putra Malaysia

About this trial

This study aims to develop, implement, and evaluate an educational program-based intervention on the knowledge, attitude, and practice toward renal nutrition among dietitians working with chronic kidney disease (CKD) patients in public hospitals in Saudi Arabia. The study hypothesizes that there will be a significant improvement in the knowledge, attitude, and practice of renal nutrition among the dietitians in the intervention group compared to the control group after the implementation of the educational program. The findings will contribute to enhancing the ability of dietitians to provide effective nutritional care and support for CKD patients in Saudi Arabia.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Dietitians who worked with chronic kidney disease patients.

Dietitians who registered in Saudi Commission for Health Specialties.

Completed at least one-year experience in their job.

Dietitians who agree to participate in the study.

Disqualifiers

Medical doctor dietitians.

Internship and student.

Dietitians under one-year experience.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Education intervention

    Other intervention

    Knowledge, Attitude, and Practice Questionnaire (KAPQ) Regarding Renal Nutrition will be used to collect the data at baseline, after the intervention, and three months follow-up, which is adjusted for clustering.

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: Education intervention programOther 1 intervention
Group B: No Intervention: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Improved in Knowledge Regarding Renal Nutrition

A structured assessment designed to evaluate knowledge and perception of nutrition care including dietary guidelines, nutrient functions, and health benefits will be explored. The assessment consists of 25 questions, each aimed at gauging the respondents' understanding of various aspects of nutrition. Each question will have multiple-choice answers, with one correct answer and several distractors. The best answer will be coded as "1" and the wrong answer as "0". There will be a maximum score of 25 and a minimum of 0.

Time frame
Timepoint 1 = Baseline. Timepoint 2 = After the intervention (one week post intervention). Timepoint 3 = three months follow-up ( 12 weeks)
2

Improved in Attitude Regarding Renal Nutrition

The assessment of attitudes regarding renal nutrition among dietitians will be conducted using a structured questionnaire based on a Likert scale. This approach allows for the quantification of attitudes related to renal diets, which is crucial for evaluating dietitians' perspectives and enhancing their counselling strategies. The proposed questionnaire will consist of 45 questions categorized into five Likert scale options: 1= Never, 2= Rarely, 3=Sometimes, 4 = Often, 5= Always. The scoring system for the questionnaire will range from a minimum score of 45 (if all responses are "Never") to a maximum score of 225 (if all responses are "Always").

Time frame
Timepoint 1 = Baseline. Timepoint 2 = After the intervention (one week post intervention). Timepoint 3 = three months follow-up ( 12 weeks)
3

Improved in Practice Regarding Renal Nutrition

This section involvoes 45 questions related to nutrition care practices. Each question has five possible answers: Never, Rarely, Sometimes, Often, and Always. The response options: Never (1 point), Rarely (2 points), Sometimes (3 points), Often (4 points) and Always (5 points). The total score can range from a minimum of 45 (if all responses are "Never") to a maximum of 225 (if all responses are "Always").

Time frame
Timepoint 1 = Baseline. Timepoint 2 = After the intervention (one week post intervention). Timepoint 3 = three months follow-up ( 12 weeks)

Secondary outcomes

Other outcomes

Sponsors and contacts

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