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No ConditionsNCT06862466

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

A study testing Education intervention in people with No Conditions, run by Universiti Putra Malaysia at 1 site in Malaysia.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 80 yearsHealthy volunteers can take part
Conditions the study is for
No Conditions
What is being tested?
Education intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteMalaysia
Study dates
1 Mar 2024to 30 Dec 2025
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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.
  • Dietitians who are available at the time of data collection.

Who cannot join

  • Medical doctor dietitians.
  • Internship and student.
  • Dietitians under one-year experience.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Malaysia1 site, 1 recruiting
  • Universiti Putra Malaysia

    Serdang, Selangor, 43300

    Zulfitri 'Azuan Mat Daud, PhD, +603-9769 12444, zulfitri@upm.edu.my

    Shatha Alattar, Master, +966555604580, GS66695@upm.edu.my

    Recruiting

Other trials in Malaysia

About this study

Official title: Impact Of An Intervention Education Program On The Knowledge, Attitudes, And Practices Of Dietitians Working With Chronic Kidney Disease Patients In Public Hospitals Of Saudi Arabia

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.

Read the detailed description

A cluster randomized controlled trial will be conducted to evaluate the effectiveness of the intervention on the level of knowledge, attitude, and practice in renal nutrition competencies among the dietitians. A total of 100 participants (50 participants for each group) will be select using simple random sampling.

The education intervention program will be developed based on the literature review of the guidelines for the nutritional management of CKD by looking into all evidence-based practice guidelines of renal medical nutrition therapy. The education intervention will include five weeks of in-person education sessions. The education intervention program will cover five lessons including nutrition assessment for CKD, malnutrition, macro- and micronutrients deficiencies in CKD, nutrition intervention and counselling skills. The education program will be delivered through lectures, workshops, brainstorming and case studies using materials such as PowerPoints, videos, cards, posters, booklets and activities. The program will be offered online via Zoom software, and the learners will have the materials to review at home. The program will be provided in close collaboration between the researcher and the hospital's nutrition department.

Data will be collected from four selected public hospitals in Jazan city, Saudi Arabia, by direct interview of the dietitians in the hospitals to determine the competency assessment on knowledge, attitude, and practice of renal nutrition. All respondents in the hospitals will be evaluated before the start of the program (baseline evaluation), after the final intervention session (post-intervention evaluation), and three months after intervention (three-month follow-up after intervention). Data will be analyzed by using the software Statistical Package for Social Sciences (SPSS) version 26.

Conditions
No Conditions
Being tested
Education intervention

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Education interventionOther

    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.

Study groups in NCT06862466
Study groupRoleWhat they receive
Education intervention programOtherThe intervention group will have an education intervention program which will cover five lessons including nutrition assessment for CKD, malnutrition, macro- and micronutrients deficiencies in CKD, nutrition intervention and counselling skills. The education program will be delivered through lectures, workshops, brainstorming and case studies using materials such as PowerPoints, videos, cards, posters, booklets and activities. The program will be offered online via Zoom software, and the learners will have the materials to review at home. The program will be provided in close collaboration between the researcher and the hospital's nutrition department.
Receives: Other: Education intervention
No Intervention: Control groupNo interventionThe control group will not have any intervention.

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 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").

    Measured: 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").

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

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Mar 2025
  2. Study start1 Mar 2024
  3. Primary completion1 Oct 2025 (estimated)
  4. Study completion30 Dec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Model description
A cluster randomized controlled trial
Masking
Single blind
Who is masked
Participant
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06862466
Sponsor's protocol ID
UPM-PhDSAlattar
Status last verified
Mar 2025
First submitted
2 Mar 2025
Last updated
6 Mar 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Education intervention in people with No Conditions, run by Universiti Putra Malaysia at 1 site in Malaysia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Malaysia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Improved in Knowledge Regarding Renal Nutrition (time frame: Timepoint 1 = Baseline. Timepoint 2 = After the intervention (one week post intervention). Timepoint 3 = three months follow-up ( 12 weeks)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Mar 2025.

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