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NCT Number: NCT07493642

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

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:

* 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.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Fu Jen Catholic University Hospital

New Taipei City, Taishan District, 243, Taiwan

Location status: Recruiting

Location contact

HUEI SHIN WEN

CONTACT

[email protected]

+886963012591

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

Multimedia Health Education

Behavioral

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 Group

Behavioral

Standard CKD Education

Primary outcomes

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

    Time frame: Baseline and 12 weeks after intervention

Secondary outcomes

  1. Physical activity level (IPAQ-C)

    Time frame: Baseline and 12 weeks after intervention

    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.

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

    Time frame: 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.

    Time frame: Baseline and 12 weeks after intervention

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

    Time frame: Baseline and 12 weeks after intervention

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

    Time frame: Baseline and 12 weeks after intervention

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

    Time frame: Baseline and 12 weeks after intervention

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

    Time frame: Baseline and 12 weeks after intervention

Study contacts

Contact information is provided by the study sponsor or research team.

HUEI SHIN WEN

CONTACT

[email protected]

+886963012591

Sponsors and collaborators

Lead sponsor

Fu Jen Catholic University Hospital

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 25, 2026
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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