Actively Recruiting

Phase Not Applicable
Age: 20Years - 70Years
All Genders
Healthy Volunteers
NCT07243717

Information-Assisted Intervention for Potential Living Kidney Donors

Led by National Taipei University of Nursing and Health Sciences · Updated on 2026-04-08

45

Participants Needed

1

Research Sites

70 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effectiveness of an information-assisted intervention in enhancing knowledge, decision self-efficacy, and reducing decisional conflict among potential living kidney donors. Using a one-group pretest-posttest design, participants will be recruited from the urology and kidney transplant outpatient clinics of two hospitals in northern Taiwan. After providing informed consent and completing a baseline questionnaire (T0), participants will receive a four-week information-assisted intervention in addition to routine care, with follow-up assessments at 4 weeks (T1) and 8 weeks (T2). Data will be collected using structured questionnaires assessing decisional conflict, decision self-efficacy, knowledge, positive thinking, family resilience, and satisfaction with the intervention.

CONDITIONS

Official Title

Information-Assisted Intervention for Potential Living Kidney Donors

Who Can Participate

Age: 20Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing to undergo evaluation for living kidney donation
  • Owns a smartphone or tablet with internet access
  • Able and willing to participate in the study and provide written informed consent
Not Eligible

You will not qualify if you...

  • Deemed unsuitable for kidney donation after evaluation by a transplant specialist

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Chang Gung Memorial Hospital

Taoyuan, Taiwan, 333

Actively Recruiting

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Research Team

C

Ching-Hui Chien, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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