Skip to main content
OpenTrials
Completed

NCT Number: NCT07129083

Exploring Predictors of Quality of Life in Older Adults With End-Stage Kidney Disease Receiving In-Center Hemodialysis

This cross-sectional observational study investigates the overall quality of life (QoL) in adults aged 65 and older receiving in-center hemodialysis. While health-related quality of life (HRQoL) is commonly used in nephrology, it may not fully reflect what matters most to older patients. Using the Amnestic Comparative Self-Assessment (ACSA) as the primary measure, this study explores key determinants of QoL and examines how it relates to existing HRQoL tools (EQ-5D-3L, EORTC QLQ-C30, QLQ-MY20). Data are collected from four hospitals in Flanders, Belgium, using psychosocial (geriatric) assessments. Statistical analysis includes regression and cluster methods to identify predictors and patient subgroups. Results aim to inform more patient-centered care and improve QoL measurement in dialysis research.

Completed

Looking for future studies?

Notify Me

Key information

About this study

The global prevalence of end-stage kidney disease (ESKD) is steadily rising, with older adults representing the fastest-growing demographic in this patient population. In Europe, individuals aged 65 and older now account for over 52% of all incident ESKD cases. The primary treatment modality, in-center hemodialysis (ICHD), although life-sustaining, imposes a considerable treatment burden. This burden, when combined with the inherent symptom load of advanced kidney disease, often leads to a significant reduction in patients' overall well-being.

Compared to their younger counterparts, older adults on dialysis experience more complex clinical trajectories, characterized by multi-morbidity, increased frailty, and psychosocial vulnerability. Moreover, this population often faces challenges in adhering to the demanding schedules and lifestyle restrictions associated with dialysis. These factors collectively contribute to a reduction in overall quality of life (QoL), which patients often prioritize even over life expectancy.

Numerous studies have demonstrated that many older dialysis patients are willing to trade significant lengths of life expectancy, up to nine years in some cases, in exchange for better QoL. Despite this, QoL remains a vastly underutilized metric in nephrology clinical research. Only a small fraction of randomized controlled trials include QoL as an outcome measure, and even fewer consider it as a primary endpoint.

Health-Related Quality of Life (HRQoL), a narrower construct within the broader domain of QoL, is often used as a proxy for evaluating the well-being of patients. However, HRQoL tools may not fully capture what matters most to patients, especially during major life transitions such as dialysis initiation. Furthermore, differences in HRQoL instruments can produce inconsistent evaluations of patient outcomes and influence the estimation of quality-adjusted life years (QALYs), potentially skewing health policy decisions.

In light of these concerns, there is a need to examine overall QoL among older adults receiving dialysis, moving beyond standard HRQoL assessments to capture a more holistic and patient-centered understanding of life quality in this vulnerable population.

This study aims to:

  • Identify the key determinants of overall QoL in older adults undergoing ICHD.
  • Examine how overall QoL relates to existing HRQoL measures.
  • Evaluate whether existing HRQoL instruments adequately capture domains that are meaningful to this population.
  • Explore natural groupings (clusters) of patients based on QoL and associated variables to inform future patient-centered interventions.

Study Design This is a cross-sectional, observational study reported in accordance with the Strengthening The Reporting of Observational Studies in Epidemiology (STROBE) guidelines. The study involves quantitative data collection through a structured assessment set administered face-to-face during dialysis sessions.

Participants are recruited from four hospitals in the Flanders region of Belgium between January and April 2018. Hospitals are selected to ensure a representative sample across urban, rural, academic, and regional settings.

Eligibility criteria include:

Age ≥65 years Receiving ICHD Able to provide informed consent Sufficient cognitive and language capacity to complete the questionnaire in Dutch

Exclusion criteria

include:

Receiving dialysis due to an acute hospital admission Diagnosed with severe psychiatric or cognitive disorders (e.g., dementia) as documented in the medical record

Data Collection and Outcome Measures A total of 95 variables are assessed across multiple domains, guided by the International Classification of Functioning, Disability and Health (ICF) framework. Assessments are conducted during one to three consecutive dialysis sessions, depending on each participant's physical and cognitive condition. Each session lasts approximately 45 minutes.

An independent researcher with no clinical ties to the patient or dialysis unit conducts all interviews to reduce bias and minimize socially desirable responses.

Primary Outcome Measure Amnestic Comparative Self-Assessment (ACSA): A self-anchoring QoL rating scale ranging from -5 (worst period of life) to +5 (best period), based on the individual's life experiences. Participants reflect on the most positive and negative periods of their life and rate their current quality of life relative to these anchors. This tool allows for a highly individualized and sensitive measure of overall QoL.

Secondary Measures (Independent Variables) Sociodemographic Variables: Age, sex, education level, marital status, living situation Dialysis-Related Variables: Duration of dialysis, comorbidity index, dialysis adequacy Comprehensive Geriatric Assessment (CGA): Functional, psychological, and social domains including Fall Risk: STRATIFY scale, Psychological Measures: Geriatric Depression Scale (GDS-4), Nutritional Status: Nutritional Risk Screening (NRS-2002) Frailty Assessment: Groningen Frailty Indicator (GFI) Functional Status: Brussels Integrated Activity Scale (BIA) - measuring basic, instrumental, and advanced ADLs

HRQoL Instruments:

EuroQol 5-Dimension 3-Level Questionnaire (EQ-5D-3L) European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) EORTC QLQ-Myeloma Module (QLQ-MY20)

Statistical Analysis

All data are analyzed using SPSS (version 29.0.2.0). Missing values are handled using listwise deletion per questionnaire. The analysis is carried out in four stages:

  • Descriptive Statistics: Means and standard deviations for normally distributed variables, medians and interquartile ranges for non-normal distributions. Normality assessed via Shapiro-Wilk test.
  • Univariate Analyses:

Mann-Whitney U test for dichotomous variables Kruskal-Wallis test for categorical variables with more than two groups Spearman's correlation for continuous and ordinal variables

  • Multivariate Regression: Variables significantly associated with ACSA scores in univariate analysis are entered into a stepwise linear regression model to identify independent predictors of QoL.
  • Cluster Analysis: Hierarchical clustering (Ward's method) is used to determine optimal grouping, followed by K-means clustering to explore patterns of QoL across patient subgroups.

Ethical Considerations This study was reviewed and approved by the Ethical Committee of Ghent University Hospital (B670201837264). All participants are fully informed of the study's purpose and procedures and provided both written and verbal informed consent. The study complies with the Declaration of Helsinki on ethical principles for medical research involving human subjects.

Significance and Expected Outcomes

This study offers an exploration of overall QoL in older adults receiving hemodialysis. By using the ACSA alongside commonly used HRQoL instruments and a wide range of biopsychosocial variables, the findings will help:

  • Clarify which factors most strongly influence QoL in this population
  • Reveal potential mismatches between standardized HRQoL measures and patients' lived experiences
  • Inform future intervention design focused on improving well-being, not just clinical outcomes
  • Provide empirical evidence to guide the choice of QoL instruments in research and policy evaluation, including cost-effectiveness studies

Ultimately, the study is expected to contribute to more patient-centered care models and improve the integration of QoL measures into nephrology research and clinical practice.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 65 years or older
  • Receiving maintenance in-center hemodialysis (ICHD)
  • Able to provide informed consent
  • Sufficient cognitive capacity to understand and answer study questions
  • Fluent in Dutch (able to complete assessments in Dutch)

Exclusion criteria

  • Receiving ICHD due to an acute hospital admission (not chronic treatment)
  • Documented diagnosis of severe psychiatric illness or severe cognitive impairment (e.g., dementia)
  • Unable to understand or respond adequately to the questionnaire

Treatment and study plan

Structured assessment interview

Other

Participants completed a structured, in-person assessment conducted during one to three dialysis sessions. The assessment included validated instruments to measure overall quality of life (ACSA), health-related quality of life (EQ-5D-3L, EORTC QLQ-C30, QLQ-MY20), and various clinical, psychological, functional, and sociodemographic factors.

Primary outcomes

  1. Quality of Life - Amnestic Comparative Self-Assessment (ACSA)

    Time frame: Baseline

    A self-anchoring Quality of Life scale ranging from -5 (worst time in life) to +5 (best time in life). Participants reflect on their personal best and worst life periods and rate their current QoL accordingly.

Secondary outcomes

  1. Age

    Time frame: Baseline

    Age (in years)

  2. Marital status

    Time frame: Baseline

    Marital status (single, married, widowed)

  3. Living situation

    Time frame: Baseline

    Living situation (independently alone, independently with family, in a care facility)

  4. (Grand)children

    Time frame: Baseline

    (Grand)children (yes/no, number of children and grandchildren)

  5. Dialysis vintage

    Time frame: Baseline

    Dialysis vintage up to baseline measure (in months)

  6. Hospital admissions

    Time frame: Baseline

    Hospital admissions (amount in the last year)

  7. Risk of falls

    Time frame: Baseline

    St. Thomas's Risk Assessment Tool in Falling Elderly Inpatients (STRATIFY); minimum score = 0, maximum score = 5; higher score indicates a higher risk of falling

  8. Risk of dementia

    Time frame: Baseline

    Risk of dementia using Mini-Cog (full name); minimum score = 0, maximum score = 5; lower score is higher risk of dementia

  9. Nutritional risk

    Time frame: Baseline

    Nutritional risk using the Nutritional Risk Screening 2002 (NRS-2002); minimum score = 0, maximum score = 7; lower score (<3) = lower nutritional risk

  10. Experienced level of pain

    Time frame: Baseline

    Pain, measured using a VAS-scale (from 0= no pain, to 9= worst pain imaginable)

  11. Vision impairment

    Time frame: Baseline

    Potential vision impairment, measured using two questions: 1. Do you have vision problems?; 2. Do you wear glasses?

  12. Hearing impairment

    Time frame: Baseline

    Potential hearing impairment, measured using two questions: 1. Do you have hearing problems?; 2. Do you use hearing aids?

  13. Continence problems

    Time frame: Baseline

    Potential continence problems, measured using two questions: 1. Do you have problems with continence?; 2. Do you use continence material?

  14. Frailty

    Time frame: Baseline

    The Groningen Frailty Indicator (GFI), a multidimensional frailty measure; minimum score = 0, maximum score = 15; Higher score (≥4) implies (higher levels of) frailty

  15. Activity

    Time frame: Baseline

    Brussels Integrated Activity Scale (BIA), measuring basic-, instrumental-, and advanced activities of daily living; Minimum score = 0 (completely dependent in all activities), maximum score = 54 (completely independent in all activities); Higher score = better functional status / greater independence

  16. Health-Related Quality of Life: EQ-5D-3L

    Time frame: Baseline

    Health-related quality of life assessed using the EuroQol 5-Dimension 3-Level questionnaire (EQ-5D-3L); includes 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression), rated at 3 levels (1= no problems, 2= some problems, 3= unable to/extreme problems). These can be converted into a utility score ranging from +- -0.59 to 1.00 (higher = better health). The EQ5D also includes a VAS-scale, where self-perceived health is rated from 0 (worst) to 100 (best)

  17. Health-Related Quality of Life using the EORTC QLQ-C30

    Time frame: Baseline

    The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30 (EORTC QLQ-C30) measures health-related quality of life through 5 functional, 9 symptom, and 1 global health status scale; minimum score = 0, maximum score = 100 (for functional scales, higher is better; for symptom scales, lower is better)

  18. Health-Related Quality of Life: EORTC QLQ-MY20

    Time frame: Baseline

    The European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Multiple Myeloma Module (EORTC QLQ-MY20) measures functioning and symptoms; minimum scores = 0; maximum scores = 100; for all scales, a higher score = worse outcomes (unlike the QLQ-C30 where functional scales mean better functioning)

Sponsors and collaborators

Lead sponsor

University Ghent

Other

Registry information

Official study title

Exploring Predictors of Quality of Life in Older Adults With End-Stage Kidney Disease Receiving In-Center Hemodialysis: A Cross-Sectional Analysis of Sociodemographic, Dialysis-specific, Biopsychosocial, and Activity-Related Factors

Acronym: B670201837264

Important dates

Study start
2018
Primary completion
2018
Study completion
2025
First posted
Aug 19, 2025
Registry last updated
Aug 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.