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. 2024 Mar 20;17:91–104. doi: 10.2147/IJNRD.S387598

Table 1.

Current Clinical Trials Addressing Symptom Management in Haemodialysis Patients

Study Patient Population Intervention Outcome
Roumelioti et al 201878 150 adult haemodialysis patients from Pennsylvania and New Mexico Two-site parallel group randomised controlled trial comparing a 12-week stepped collaborative care intervention [includes Cognitive Behavioural Therapy (CBT)] with a control arm of technology-delivered health education. The delivery of CBT will be with live videoconferencing. Patient symptoms, health-related quality of life, treatment adherence and inflammatory biomarkers,
Johnson et al 202079 Participants from eligible (in-centre haemodialysis with clinicians able to review patient-reported data) haemodialysis units in Alberta and Ontario. Multi-centre randomised controlled trial to evaluate the use of disease-specific and generic patient-reported outcome measures (PROMs). The patients will be randomised to one of four groups: 1) complete a dialysis specific PROM, 2) complete a generic PROM, 3) complete both types of PROMs, 4) receive usual care with no PROMs. The primary outcome is improvement in patient-provider communication with secondary outcomes of patient symptom management, use of healthcare service and cost-effectiveness.
Unruh et al 202080 126 adult participants treated with haemodialysis in community-based facilities in Seattle and Alburquerque with chronic insomnia Patients will be randomised 1:1:1 over 31 months to either a 6- week treatment with CBT, trazodone, or placebo. Short term improvement in insomnia at 6 weeks and long-term effectiveness at 25 weeks.
Greenham et al 202281 Up to 2400 adult haemodialysis participants from 143 satellite haemodialysis centres in Australia and New Zealand. Registry-based cluster randomised controlled trial to determine the clinical and cost effectiveness of symptom monitoring using the Integrated Palliative Outcome Scale-Renal (IPOS-Renal) survey. Patients in the intervention arm will complete the IPOS-renal survey 3-monthly over a 12-month period. Change in health-related quality of life as measured by the EQ-5D-5L and compared between the intervention and control arm. Secondary outcomes are dialysis withdrawal, overall survival, fatigue, cause-specific mortality, symptom severity, haemodialysis duration and adequacy and cost-effectiveness,