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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
The Evaluation of Change in Psychosocial Risk With Caregivers of Children With Chronic Kidney Disease: A Short-term
Caroline C Piotrowski1, Kira Kudar1, Julie Strong2
1Department of Community Health Sciences, University of Manitoba, Winnipeg, Canada.
Insights
Caregivers of youth with chronic kidney disease (CKD) faced increased psychosocial risk during the COVID-19 pandemic, yet demonstrated resilience. This study highlights the value of mixed-methods research in understanding family experiences during health crises.
Area of Science:
- Pediatric Nephrology
- Psychosocial Health
- Public Health Emergencies
Background:
- The COVID-19 pandemic exacerbated challenges for caregivers of young people with chronic kidney disease (CKD).
- New concerns arose for these families during the pandemic, with limited understanding of their coping mechanisms.
- Caregiver experiences pre- and post-transplant for pediatric CKD patients during the pandemic remain under-explored.
Purpose of the Study:
- To assess changes in psychosocial risk among families of young individuals with CKD during the COVID-19 pandemic.
- To evaluate caregiver perspectives on managing pandemic-related adversities.
- To explore the impact of transplant status on psychosocial risk during the health emergency.
Main Methods:
- A longitudinal mixed-methods study design was employed in Manitoba, Canada.
- Caregivers (n=36 pre-pandemic, n=13 during pandemic) completed the Psychosocial Assessment Tool (PAT) and interviews.
- Quantitative PAT scores and qualitative interview data were analyzed using thematic analysis and integrated for comprehensive understanding.
Main Results:
- Overall family psychosocial risk and caregiver problems significantly increased during the pandemic.
- Families of transplant recipients showed lower pre-pandemic psychosocial risk compared to transplant candidates.
- Qualitative analysis revealed negative and positive pandemic experiences, alongside coping strategies.
Conclusions:
- Despite increased psychosocial risk, caregivers exhibited resilience and adaptive coping mechanisms.
- Integrating quantitative and qualitative data provided valuable insights into caregiver experiences.
- Findings support the pediatric psychosocial preventive health model in understanding family well-being during crises.
Background:
The COVID-19 pandemic and its accompanying safeguards intensified many of the ongoing daily challenges faced by caregivers of young people with chronic kidney disease (CKD) both pre-transplant and post-transplant, and also created a variety of new and pressing concerns. Little is known about how these families managed this unexpected adversity in their lives.
Objective:
To evaluate change in psychosocial risk for families of young people with CKD during the COVID-19 pandemic health emergency from the perspective of caregivers.
Design:
A short-term longitudinal mixed-methods study with a convergent parallel design.
Setting:
Manitoba, Canada.
Participants:
Thirty-six caregivers of young people with CKD participated in a quantitative assessment prior to the pandemic; approximately half were transplant recipients. Thirteen were re-assessed during the pandemic (62% were caregivers of transplant recipients) using both qualitative and quantitative assessments.
Methods:
First, caregivers completed the Psychosocial Assessment Tool (PAT) prior to the pandemic. Second, caregivers were re-assessed using the PAT during the pandemic. They were also interviewed about their experiences. Changes in PAT scores over time were evaluated, including an investigation of whether psychosocial risk was related to transplant status. Interviews were coded using thematic analysis. In the interpretation stage, the qualitative findings were combined with the quantitative results to help explain the latter and reach a more fulsome understanding of caregivers' experience.
Results:
Quantitatively, overall family psychosocial risk scores increased significantly during the pandemic health emergency, as did the domain of Caregiver Problems. Families of transplant recipients were found to be at significantly lower psychosocial risk pre-pandemic than families of transplant candidates. Coding identified Negative Pandemic Experiences, Positive Pandemic Experiences, and Coping Mechanisms. Mixed-methods analyses revealed several areas of convergence and divergence between the quantitative and qualitative findings.
Limitations:
Limitations included a small sample size that limited generalizability, single site data collection, and single caregiver report.
Conclusions:
Although overall family psychosocial risk increased during the pandemic, caregivers described several resilience processes and characteristics. A mixed-method approach provided a unique perspective that highlighted the value of integrating quantitative and qualitative findings. Results were discussed within the pediatric psychosocial preventive health model framework.
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