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Cognitive behavioral therapy for hyperkalemia in maintenance hemodialysis patients: a prospective, single center, randomized controlled trial

Cognitive Behavioral Therapy for Hyperkalemia in Hemodialysis Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122754
Enrollment
Unknown
Registered
2026-04-17
Start date
2026-04-20
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperkalemia

Interventions

intervention group:Interventions in the experimental group were delivered via a smartphone application centered on cognitive behavioral therapy (CBT), consisting of two phases: Phase 1 (Weeks 1–2): Id
control group:Clinicians provide patient education via PowerPoint presentations on tablet computers and distribute educational brochures to patients. Week 1: Disease knowledge education Patients recei

Sponsors

The First Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1.Age >= 18 years; 2.Undergoing regular hemodialysis for > 3 months; 3.At least one episode of hyperkalemia (venous serum potassium > 5.5 mmol/L) in the past year; 4.Able to operate a smartphone and complete the assessment scales independently; 5.Provision of written informed consent prior to study enrollment.

Exclusion criteria

Exclusion criteria: 1.Severe visual, hearing, language, or cognitive impairments, or a history of mental disorders; 2.Planned changes in dialysis modality during the study period; 3.Participation in other clinical trials that could affect the study outcomes.

Design outcomes

Primary

MeasureTime frame
Serum potassium concentration ;Adverse outcomes occurred in study participants within 12 weeks;

Countries

China

Contacts

Public ContactHongli Lin

The First Affiliated Hospital of Dalian Medical University

linhongli@vip.163.com+86 159 4097 5840

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026