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INCremental Dialysis to Improve Health Outcomes in People Starting Haemodialysis (INCH-HD)

The INCremental Dialysis to Improve Health Outcomes in People Starting Haemodialysis (INCH-HD) Study: a Randomised Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04932148
Enrollment
372
Registered
2021-06-18
Start date
2022-07-06
Completion date
2026-08-01
Last updated
2026-05-13

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

Conditions

Kidney Failure

Keywords

Incremental HD, Incident HD

Brief summary

The INCH-HD trial will test if incremental HD preserves the quality of life of patients and families and is a safe, practical, cost effective treatment option.

Detailed description

Kidney failure is a growing public health problem and fatal unless treated with dialysis or transplantation. Haemodialysis is the most common treatment for kidney failure in Australia and globally. Patients find haemodialysis extremely burdensome due to symptoms like fatigue, pain, cramps and poor quality of life that generally equates to \<60% of full health. Furthermore, haemodialysis is associated with an extremely high mortality (\<50% survive 5 years), particularly in the first 3-6 months of starting haemodialysis, which is likely linked to the rapid loss of patients' own kidney function when starting haemodialysis abruptly at three sessions/week. Observational studies suggest that starting haemodialysis incrementally at two sessions/ week is associated with lower mortality and better preservation of patients' remaining kidney function while offering many patient-important advantages, including dialysis free time and ability to work. However, robust evidence to recommend this incremental approach is lacking. The INCH-HD study is an investigator-initiated, international, multicentre, prospective, adaptive, randomised, open-label, parallel group, non-inferiority trial. The primary objective of the study is to demonstrate whether incremental HD is non-inferior to conventional HD for the patient-important outcome of quality of life measured using Kidney-specific component of the Kidney Disease Quality of Life - Short Form measurement (KDQOL-SF) at 6 months from dialysis commencement. The study will recruit a total of 372 participants across HD centres in Australia, and Canada. The outcomes of this trial will will provide urgently needed high quality evidence on whether starting haemodialysis incrementally at two sessions/week compared to the conventional three sessions/week can safely reduce the physical, financial and quality-of life burden on patients, lower early mortality rates and slow loss of kidney function while increasing haemodialysis capacity and reducing costs.

Interventions

OTHERIncremental HD

Starting haemodialysis at twice weekly frequency

Starting haemodialysis at thrice weekly frequency

Sponsors

The University of Queensland
Lead SponsorOTHER
Medical Research Future Fund
CollaboratorOTHER
Queensland Health
CollaboratorOTHER_GOV
Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Adults (≥ 18 years of age) and 2. Commencing HD as their initial dialysis therapy and 3. Able to give informed consent

Exclusion criteria

1. Urine output \<0.5Litres/day 2. Unlikely to be on HD for ≥1 year.

Design outcomes

Primary

MeasureTime frameDescription
Heath related quality of life6 monthsThis will be measured using Kidney-specific component (KSC) of the Kidney Disease Quality of Life Short Form (KDQOL-SF) V1.3 questionnaire. The KSC is the mean of the 11 domains of the kidney-disease specific items of KDQOL-SF. Scores are transformed onto a 0-100 range, where a higher score reflects a better quality of life.

Secondary

MeasureTime frameDescription
Residual kidney function (RKF)Baseline, 3, 6, 12 and 18 monthsCalculated as (creatinine clearance + kidney urea clearance) divided by 2 then corrected for body surface area using the DuBois method (0.20247 x (height in centimetres x 0.725) x (weight in kilograms x 0.425). Expressed as millilitres per minute (ml/min). Expected range 1 ml/min to 20 ml/min, where lower values indicate worse kidney function.
Healthcare resource utilisationBaseline to 18 monthsHealthcare resource use over 18 months using linked data and patient monthly calendars
Healthcare costsBaseline to 18 monthsHealthcare costs over 18 months using linked data and patient monthly calendars
Heath related quality of life using Kidney Disease Quality of Life Short Form (KSQOL-SF) questionnaireBaseline, 3, 6, 9, 12, 15 and 18 monthsHeath-related quality of life will be measured using Kidney-specific component (KSC) of the Kidney Disease Quality of Life Short Form (KDQOL-SF) V1.3 questionnaire. The KSC is the mean of the 11 domains of the kidney-disease specific items of KDQOL-SF. Scores are transformed onto a 0-100 range, where a higher score reflects a better quality of life.
Heath related quality of life using EuroQol 5-dimension 5-level (EQ-5D-5L) questionnaireBaseline, monthly to 18 monthsHeath-related quality of life will be measured using EuroQol 5 Domain 5 Level (EQ-5D-5L) questionnaire. EQ-5D has descriptive and visual analogue scale (VAS). Descriptive system consists of five dimensions mobility, self-care, usual activities, pain/discomfort and anxiety/depression. VAS records patient's self-rated health on vertical visual analogue scale with endpoints best to worst health with 0 being worst and 100 being best health.
Incidence of all-cause mortalityBaseline to 18 monthsIncidence of all-cause mortality up to 18 months
Time to major cardiovascular event (MACE)Baseline to 18 monthsTime to first major cardiovascular event (MACE) up to 18 months
Number of non-elective hospital admissionsBaseline to 18 monthsNumber of non-elective hospital admissions up to 18 months
Total hospital daysBaseline to 18 monthsTotal hospital days up to 18 months
Time to deathBaseline to 18 monthsTime to death up to 18 months
Number of hospital admissionsBaseline to 18 monthsNumber of hospital admissions up to 18 months
Adverse events and side-effectsBaseline to 18 monthsThis will include episodes of hyperkalaemia, extra dialysis sessions for fluid overload, number of vascular access complications
Symptom scoresBaseline, 3, 6, 9, 12, 15 and 18 monthsThis will be measured using change in the physical and mental component summaries of the Kidney Disease Quality of Life Short Form (KDQOL-SF) V1.3 questionnaire. This is scored using the mean of the physical and mental components of the KDQOL-SF. Scores are transformed onto a 0-100 range, where a higher score reflects a better quality of life.
FatigueBaseline, 3, 6, 9, 12, 15 and 18 monthsThis will be measured using the Standardised Outcomes in Nephrology-Haemodialysis (SONG-HD) Fatigue questionnaire. The SONG-HD Fatigue measure consists of three items that assess the effect of fatigue on life participation, tiredness, and level of energy. The overall score for fatigue is obtained by summing the responses across the three questions, resulting in a scale ranging from zero (no fatigue) to nine (maximum fatigue).
Nutritional StatusBaseline, 6, 12 and 18 monthsThis will be measured using the Subjective Global Assessment (SGA) of nutrition which is scored as proportion of well nourished (A) versus malnourished (B or C). A (well nourished), B (mildly-moderately malnourished), C (Severely malnourished)
Vascular accessBaseline to 18 monthsThis will be measured as mumber of functional vascular access interventions required per patient per year to enable and /or maintain vascular access for HD per patient-year

Countries

Australia, Canada

Contacts

CONTACTLisan Mulvey
inch-hd.trial@uq.edu.au+61 417 690 237
PRINCIPAL_INVESTIGATORPeter Kerr, Prof

University of Queensland, Monash University

PRINCIPAL_INVESTIGATORDavid Johnson, Prof

University of Queensland, Queensland Health

PRINCIPAL_INVESTIGATORAndrea Viecelli, Dr

University of Queensland, Queensland Health

PRINCIPAL_INVESTIGATORCharmaine Lok, Prof

University Health Network, Toronto

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 14, 2026