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Symptom Assessment And Management For Adults With CKD In Vietnam (SAM-CKD)

G

Griffith University

Status

Not yet enrolling

Conditions

Chronic Kidney Disease

Treatments

Device: Symptom Assessment and Management Program (SAM-CKD) which is delivered via Smart Kidney mobile app

Study type

Interventional

Funder types

Other

Identifiers

NCT07186361
135/2025/CN/HDDD VMEC

Details and patient eligibility

About

Adults with chronic kidney disease (CKD) have many symptoms that lower their quality of life and put a huge burden on the healthcare system. Recently, eHealth solutions have been introduced in chronic kidney disease care, helping with symptom management and improving patient outcomes. While symptom management via electronic health (eHealth) is emerging in other countries, it has not commenced in Vietnam. This study aims to develop and evaluate a remote symptom assessment and management program delivered through a mobile application for adults with CKD living in Vietnam to help them manage their symptoms. This is the first intervention program focusing on symptom assessment and management in Vietnam. By assessing and managing symptoms, adults with CKD can better self-manage their symptoms.

Full description

Adults with CKD experience a wide range of symptoms that significantly impact their health-related quality of life and place a huge burden on the healthcare system. Mobile health app-based interventions for symptom assessment and management have the potential to alleviate the burden of CKD and improve patient outcomes. This study aims to develop and test a Symptom Assessment and Management (SAM-CKD) program embedded into a mobile app for adults with CKD living in Vietnam. A feasibility randomised trial will be designed in designed following the Consolidated Standards of Reporting Trials (CONSORT) statement extension for randomised pilot and feasibility trials to evaluate the feasibility, usability, acceptability, and potential effectiveness of symptoms and health-related quality of life. Adults with CKD grade 4 or 5 (including those on dialysis) will be randomly assigned to either the intervention or control groups. Informed by the Theory of Symptom Management, the intervention includes three main components: a general introduction to CKD symptoms, a symptom tracker, and symptom management strategies. The intervention group will use the program for 6 weeks to self-manage their symptoms. Primary outcomes are feasibility and acceptability, measured by eligibility rate, recruitment rate, retention and attrition, protocol adherence, mobile app usability and acceptability. Secondary outcomes are changes in CKD symptoms and health-related quality of life measured by Integrated Palliative Outcome Scale - Renal (IPOS-Renal) and European Quality of Life 5-Dimension 5-Level Questionnaire (EQ-5D-5L), respectively. Data analysis involves descriptive and intention-to-treat analyses. The results will be reported following the CONSORT statement extension for randomised pilot and feasibility trials. Findings will provide empirical evidence about the feasibility, acceptability and initial effectiveness of mobile-based symptom management intervention and will inform the design of future large-scale effectiveness studies.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged 18 years or above
  • are diagnosed with CKD grade 4 or grade 5 with or without haemodialysis
  • speak and read Vietnames
  • own a smartphone operating on Android with internet accessibility
  • agree to participate in this study.

Exclusion criteria

  • cognitive impairment
  • psychological problems
  • terminal illness, such as cancer and advanced lung disease
  • acutely unwell
  • participating in another study during this trial

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Intervention group (SAM-CKD group)
Experimental group
Description:
The intervention group will be invited to use the SAM-CKD program for 6 weeks
Treatment:
Device: Symptom Assessment and Management Program (SAM-CKD) which is delivered via Smart Kidney mobile app
Control group
No Intervention group
Description:
Participants in the control group will receive usual care and they will be offered to use the intervention after the study completes

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Khanh Linh Bui, Master of Science in Nursing

Data sourced from clinicaltrials.gov

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