Workstream 1 (main randomised controlled trial) |
Inclusion criteria: |
• Adults (≥ 18 years); |
• End-stage kidney failure receiving thrice-weekly in-centre haemodialysis for at least 3 months |
• Able to provide written informed consent; |
• Able participate fully in follow-up |
Exclusion criteria: |
• Currently receiving in-centre nocturnal haemodialysis; |
• < 3 months since stopping extended daytime dialysis or in-centre nocturnal haemodialysis; |
• Extended-hours haemodialysis is clinically indicated (e.g. calciphylaxis, pregnancy) |
• Scheduled living-donor transplant in the next 6 months; |
• Plans to change dialysis modality in the next 6 months; |
• Life expectancy < 6 months; |
• Current participation in an interventional trial with conflicting therapies or primary outcome |
Workstream 2 (Process Evaluation) |
Staff inclusion criteria |
• Clinical and non-clinical staff working at haemodialysis units participating in the NightLife study; |
• Adults (≥ 18 years); |
• Ability to give written informed consent; |
• Ability and willingness to participate fully in the observations and interviews |
Relative/visitor inclusion criteria |
• Relatives or visitors accompanying patients (that fulfil workstream 1 eligibility criteria) to haemodialysis sessions; |
• Adults (age ≥ 18 years); |
• Ability to give written informed consent; |
• Ability and willingness to participate fully in the observations and interviews |
Workstream 3 (QuinteT recruitment intervention) |
Staff inclusion criteria |
• Clinical and non-clinical staff working involved in overseeing or recruiting to the NightLife study; |
• Adults (≥ 18 years); |
• Ability to give informed consent |