Effect of Pecha Kucha Education on Fluid and Diet Adherence in Hemodialysis Patients
Effect of Pecha Kucha-Based Education on Fluid and Dietary Adherence and Clinical Outcomes in Hemodialysis Patients: A Randomized Controlled Trial
1 other identifier
interventional
70
0 countries
N/A
Brief Summary
This randomized controlled trial aims to evaluate the effect of education based on the Pecha Kucha presentation technique on fluid and dietary adherence in patients undergoing hemodialysis. Patients receiving hemodialysis often experience difficulties in adhering to fluid and dietary restrictions, which may lead to adverse clinical outcomes. The Pecha Kucha technique is a structured, visually supported presentation format designed to improve understanding and retention of information. In this study, patients in the intervention group will receive education using the Pecha Kucha method, while the control group will receive standard education routinely provided in the dialysis unit. The study will assess whether this innovative educational approach improves adherence to treatment and clinical parameters. The findings are expected to contribute to improving patient education strategies in hemodialysis care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2026
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2026
CompletedFirst Submitted
Initial submission to the registry
April 2, 2026
CompletedFirst Posted
Study publicly available on registry
April 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2027
April 8, 2026
April 1, 2026
8 months
April 2, 2026
April 2, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Fluid Adherence (Interdialytic Weight Gain)
Fluid adherence will be assessed using interdialytic weight gain measurements obtained from patient records between dialysis sessions.
Baseline and 4 weeks after the intervention
Secondary Outcomes (1)
Serum Potassium Level
Baseline and 4 weeks
Study Arms (2)
Pecha Kucha Education Group
EXPERIMENTALParticipants will receive structured education using the Pecha Kucha presentation technique.
Standard Education
ACTIVE COMPARATORRoutine education provided to patients undergoing hemodialysis.
Interventions
Routine education provided to patients undergoing hemodialysis according to standard clinical practice.
A structured and visually supported educational intervention delivered using the Pecha Kucha presentation format to improve patients' understanding of fluid and dietary management.
Eligibility Criteria
You may qualify if:
- Receiving hemodialysis treatment for at least 6 months
- Aged 18 years or older
- Literate
- Willing to participate in the study
You may not qualify if:
- Cognitive or communication impairment
- Participation in a similar education program within the last 3 months
- Presence of terminal illness
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- Due to the nature of the educational intervention, blinding of participants and care providers is not feasible.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 2, 2026
First Posted
April 8, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
March 1, 2027
Last Updated
April 8, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to privacy and confidentiality considerations. The data contain sensitive patient information collected in a clinical setting, and sharing such data is restricted by ethical and institutional regulations.