Digital Dyadic Empowerment Program on Lifestyle Modification for Chronic Kidney Disease Management
- Conditions
- Chronic Kidney Diseases
- Registration Number
- NCT06756113
- Lead Sponsor
- National Cheng Kung University
- Brief Summary
The goal of this clinical trial is to find out if the Digital Dyadic Empowerment Program (DDEP) can help people with chronic kidney disease (CKD) and their care partners make healthy lifestyle changes. The main questions this study will answer are:
* Does DDEP help protect kidney function?
* Does DDEP support healthier daily habits?
Researchers will compare two groups:
* One group will receive the DDEP and get usual medical care.
* The other group will get usual medical care only.
Participants will:
* Receive usual care with or without DDEP for six months.
* Visit the clinic at the start and end of the study for health checks and tests.
* Practice healthy habits at home with or without help from DDEP.
This study aims to show if adding DDEP to regular care can make it easier for people with CKD and their care partners to live healthier lives.
- Detailed Description
This randomized controlled trial (RCT) aims to evaluate the long-term effects of the Digital Dyadic Empowerment Program (DDEP) in comparison to routine care for people with chronic kidney disease (CKD) and their significant others. The study will assess whether the DDEP can improve health outcomes such as kidney function, health-promoting lifestyle behaviors, and the quality of relationships between significant others over a six-month period. The trial will follow the Consolidated Standards of Reporting Trials (CONSORT) 2010 and CONSORT-EHEALTH guidelines to ensure rigorous reporting and transparency.
Baseline assessments will occur in a private clinic room and will include demographic information, disease-related characteristics, and self-reported measures. Participants in both groups will also complete the Trans-Theoretical Model (TTM) staging inventory to evaluate their readiness for lifestyle changes. Dyads assigned to the intervention group will receive DDEP setup instructions and training on platform use during the baseline visit. Throughout the study, dyads will be encouraged to utilize the platform for self-management tasks at home, including diet tracking, exercise planning, and monitoring blood pressure.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 208
- The patient has a diagnosis of Chronic Kidney Disease for at least six months;
- The patient can identify a helpful significant other, and both parties are willing to participate;
- The patient can communicate in Mandarin or Taiwanese.
- The significant other is a healthcare provider;
- The patient or the significant other has a mental illness diagnosis;
- The patient is currently receiving renal replacement therapies;
- Neither the patient nor the significant other uses a smartphone or the LINE messaging app.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Change from Baseline in eGFR at 6 Months (Patient-specific) Before initial intervention and 6 months after initial intervention For each patient, change from Baseline (Followup score - Baseline score) in the estimated Glomerular Filtration Rate (eGFR) by the Isotope Dilution Mass Spectrometry - Modification of Diet in Renal Disease (IDMS-MDRD) Equation at 6 months was obtained through the patient's biochemical test reports. Higher eGFR numbers generally indicate better kidney functions.
- Secondary Outcome Measures
Name Time Method Change from Baseline in CKD Stage at 6 Months (Patient-specific) Before initial intervention and 6 months after initial intervention For each patient, change from Baseline in CKD stage at 6 months was obtained by comparing the CKD stage at baseline and at follow-up, converted into the following three categories: (1) recover (e.g., from Stage 3a \[at baseline\] to Stage 2 \[at follow-up\]); (2) stable (e.g., remaining Stage 3a at both baseline and follow-up); and (3) progress (e.g., from Stage 3a \[at baseline\] to Stage 3b \[at follow-up\]).
Change from Baseline in TTM Stage at 6 Months (Patient-specific) Before initial intervention and 6 months after initial intervention For each patient, change from Baseline in TTM stage at 6 months was obtained by comparing the TTM stage of change at baseline and at follow-up, converted into the following three categories: (1) regress (e.g., from Preparation \[at baseline\] to Contemplation \[at follow-up\]); (2) maintain (e.g., remaining Action at both baseline and follow-up); and (3) advance (e.g., from Action \[at baseline\] to Maintenance \[at follow-up\]).
Change from Baseline in Health Promoting Lifestyle at 6 Months (Patient-specific) Before initial intervention and 6 months after initial intervention For each patient, change from Baseline (Followup score - Baseline score) in patient's Health Promoting Lifestyle at 6 months was assessed using the Health Promoting Lifestyle Profile-II Chinese version Revised (HPLP-IICR), a validated scale with 30 items rated on a 4-point Likert scale. The total scores range from 30 to 120, with higher scores indicate better health-promoting behavior.
Change from Baseline in Dyadic Adjustment at 6 Months Before initial intervention and 6 months after initial intervention For each participant, change from Baseline (Followup score - Baseline score) in Dyadic Adjustment at 6 months was assessed using the 7-item Dyadic Adjustment Scale (DAS-7). The first six items are rated on a 6-point scale, while the seventh item is rated on a 7-point scale. The total scores range from 0 to 36, with higher scores indicating better relationship quality.
Trial Locations
- Locations (1)
National Cheng Kung University
🇨🇳Tainan City, Taiwan