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Chronic Kidney Disease (CKD)NCT07493642

Multimedia Health Education on Physical Fitness and Physical Activity for Patients With Chronic Kidney Disease

A study testing Multimedia Health Education and Standard Education Group in people with Chronic Kidney Disease (CKD) and CKD Stage 1-3, run by Fu Jen Catholic University Hospital at 1 site in Taiwan.

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 clinical trial aims to determine whether a multimedia educational intervention can effectively improve physical fitness and physical activity levels in patients with chronic kidney disease (CKD), while also evaluating its overall outcomes. Read more about this study

Who is it for?
Ages 20 years and older
Conditions the study is for
Chronic Kidney Disease (CKD), CKD Stage 1-3
What is being tested?
Multimedia Health Education and Standard Education Group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteTaiwan
Study dates
17 Nov 2025to 31 Jul 2026
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 20 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Conscious adults aged 20 years or older who are literate and able to communicate in Mandarin or Taiwanese.
  • Diagnosed with chronic kidney disease (CKD) stage 1 to 3b according to the CKD-EPI formula and confirmed by a nephrologist.
  • Able to operate a mobile device (such as a smartphone, tablet, or computer) and have access to equipment capable of playing multimedia videos; family members or caregivers may assist if necessary.
  • Able to view and understand multimedia educational video content.

Who cannot join

  • Individuals with cognitive or psychiatric disorders that prevent understanding or adherence to the exercise program.
  • Individuals with gait instability or limb amputation who are unable to perform the exercise protocol.
  • Individuals with poorly controlled cardiovascular disease, such as heart failure, myocardial infarction, angina, arrhythmia, or those who have experienced chest pain during activity or rest within the past three months.
  • Individuals deemed unsuitable for exercise by their attending physician.
  • Individuals with poorly controlled diabetes (HbA1C > 9%) accompanied by retinopathy or foot ulcers.

Trial locations and contacts

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

Taiwan1 site, 1 recruiting
  • Fu Jen Catholic University Hospital

    New Taipei City, Taishan District, 243

    HUEI SHIN WEN, +886963012591, cvicky851122@gmail.com

    Recruiting

Other trials in Taiwan

About this study

This clinical trial aims to determine whether a multimedia educational intervention can effectively improve physical fitness and physical activity levels in patients with chronic kidney disease (CKD), while also evaluating its overall outcomes.

The study primarily seeks to answer the following questions:

Read more
  • Can multimedia education enhance CKD patients' cardiorespiratory endurance, muscle strength, flexibility, and physical activity levels?
  • Do patients receiving multimedia education demonstrate greater improvements in health behavior and fitness compared to those receiving standard education alone?

Researchers will compare a multimedia educational video program with conventional patient education to assess whether the multimedia approach helps patients maintain regular exercise and improve physical performance.

Participants will:

  • Be randomly assigned to either the multimedia education group or the standard education group.
  • Take part in a 12-week intervention and assessment period.
  • Undergo pre- and post-intervention evaluations, including:
  • Six-minute walk test, grip strength and chair-stand test, flexibility test, and body composition analysis (BMI, waist-to-hip ratio, InBody).
  • Completion of a physical activity questionnaire (IPAQ-C). The findings will be used to evaluate the clinical value of multimedia education in CKD management and to support the development of effective patient exercise education programs.
Being tested
Multimedia Health Education, Standard Education Group
Medical subject headings
Renal Insufficiency, Chronic

What participants receive

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

  • Multimedia Health EducationBehavioural

    Participants in this group will receive a multimedia exercise education program designed for patients with chronic kidney disease (CKD). The program includes instructional videos demonstrating proper exercise techniques, safety guidelines, and motivational content to encourage regular physical activity. The intervention aims to enhance participants' exercise knowledge, physical fitness, and activity levels over a 12-week period.

  • Standard Education GroupBehavioural

    Standard CKD Education

Study groups in NCT07493642
Study groupRoleWhat they receive
Multimedia Health EducationExperimentalNot described
Receives: Behavioral: Multimedia Health Education
Standard Education GroupActive comparatorStandard CKD Education
Receives: Behavioral: Standard Education Group

What is being measured

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

  1. Change in 6-minute walk test distance from baseline to 12 weeks, measured in meters.

    Measured: Baseline and 12 weeks after intervention

Secondary outcomes (7)
  1. Physical activity level (IPAQ-C)

    Change in physical activity level measured by the International Physical Activity Questionnaire - Chinese version (IPAQ-C) from baseline to 12 weeks. Total physical activity will be expressed in metabolic equivalent task minutes per week (MET-min/week), with higher scores indicating higher levels of physical activity.

    Measured: Baseline and 12 weeks after intervention

  2. Change in handgrip strength from baseline to 12 weeks, measured in kilograms.

    Measured: Baseline and 12 weeks after intervention

  3. Change in chair stand test performance from baseline to 12 weeks, measured by number of repetitions completed in 30 seconds.

    Measured: Baseline and 12 weeks after intervention

  4. Change in sit-and-reach test score from baseline to 12 weeks, measured in centimeters.

    Measured: Baseline and 12 weeks after intervention

  5. Change in waist-to-hip ratio from baseline to 12 weeks.

    Measured: Baseline and 12 weeks after intervention

  6. Change in body mass index from baseline to 12 weeks, measured in kg/m².

    Measured: Baseline and 12 weeks after intervention

  7. Change in body composition from baseline to 12 weeks, including body fat percentage and skeletal muscle mass.

    Measured: Baseline and 12 weeks after intervention

Timeline

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

  1. First posted25 Mar 2026
  2. Study start17 Nov 2025
  3. Primary completion30 Jun 2026 (estimated)
  4. Study completion31 Jul 2026 (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
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07493642
Sponsor's protocol ID
FJUH114494
Status last verified
Nov 2025
First submitted
4 Mar 2026
Last updated
25 Mar 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Multimedia Health Education and Standard Education Group in people with Chronic Kidney Disease (CKD) and CKD Stage 1-3, run by Fu Jen Catholic University Hospital at 1 site in Taiwan.

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 4 inclusion and 5 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 25 Mar 2026. 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 Taiwan. 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?

Contact HUEI SHIN WEN (+886963012591, cvicky851122@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in 6-minute walk test distance from baseline to 12 weeks, measured in meters. (time frame: Baseline and 12 weeks after intervention). 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 25 Mar 2026.

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