App-based Education Program for CKD

Not Applicable

Active, not recruiting

• Conditions: Renal Insufficiency, Chronic
• Interventions: Other: Education

• Registration Number: NCT05766644
• Lead Sponsor: Inje University

Brief Summary

A randomized control trial to test the effect of a mobile app-based educational program for Chronic Kidney Disease patients.

Detailed Description

Not available

Study Timeline

• Study Start: 2022-10-27
• Primary Completion: 2023-02-06
• Study First Submitted: 2023-02-27
• Status Verified: 2023-03
• Study First Submitted QC: 2023-03-09
• Last Update Submitted: 2023-03-09
• Study First Posted: 2023-03-13
• Last Update Posted: 2023-03-13
• Study Completion: 2023-10-06

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 129

Inclusion Criteria

• Diagnosed with CKD Stage 1~5
• Have been receiving CKD treatment for more than 6 months
• Owns an android mobile phone

Exclusion Criteria

• Diagnosed with cancer within 5 years of recruitment

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Education	Education	Enrolled in a mobile app-based education program, with guidance from a healthcare professional. All educational materials and surveys are provided via the app.

Primary Outcome Measures

Name	Time	Method
Quality of Life (SF-36v2)	48 days	36-Item Short Form Health Survey, version 2. Scores range from 0 to 100, higher value corresponding to better outcome (better quality of life)
Potassium	56 days	Serum potassium levels obtained from routine blood test.
Phosphate	56 days	Serum phosphate levels obtained from routine blood test.
MIS	55 days	10-item nutritional status measured with Malnutrition Inflammation Score. Scores range from 0 to 30, higher value corresponding to worse outcome (higher risk of malnutrition)
Albumin	56 days	Serum albumin levels obtained from routine blood test.

Secondary Outcome Measures

Name	Time	Method
Depression	55 days	21-item depression score measured with Korean-Beck Depression Inventory. Scores range from 0 to 63, higher value corresponding to worse outcome (severe depression).
Sodium intake behavior	0 days	15-item sodium intake behavior score. Scores range from 0 to 15, higher values corresponding to worse outcome (higher tendency to prefer salty food).
Insomnia	48 days	7-item insomnia score measured with Insomnia Severity Index in Korean. Scores range from 0 to 28, higher value corresponding to worse outcome (severe insomnia)
Creatinine	56 days	Creatinine levels obtained from routine blood test.
Sodium intake attitude	0 days	17-item sodium intake attitude score. Scores range from 0 to 17, higher values correspond ing to better outcome (more willing to reduce sodium intake).

Trial Locations

Locations (1)

Inje University Seoul Paik Hospital; 🇰🇷 Seoul, Korea, Republic of