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Caregiver Burden and Psychological Outcomes in Caregivers of Stroke Patients With Lower Urinary Tract Symptoms

Caregiver Burden, Fatigue, Sleep Quality, and Depression in Family Caregivers of Stroke Patients With Lower Urinary Tract Symptoms: A Cross-Sectional Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07480642
Acronym
CARE-LUTS
Enrollment
70
Registered
2026-03-18
Start date
2023-06-01
Completion date
2024-12-01
Last updated
2026-03-18

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

Conditions

Caregiver, Fatigue Syndrome, Chronic, Stroke

Brief summary

This cross-sectional observational study aims to evaluate caregiver burden, fatigue, sleep quality, and depression among family caregivers of stroke patients with lower urinary tract symptoms (LUTS). Stroke survivors frequently experience urinary dysfunction, which may increase caregiving demands and negatively affect caregiver well-being. A total of 70 family caregivers of stroke patients with LUTS receiving inpatient or outpatient rehabilitation care were included. Caregiver outcomes were assessed using validated instruments including the Caregiver Strain Index (CSI), Fatigue Severity Scale (FSS), Pittsburgh Sleep Quality Index (PSQI), and Beck Depression Inventory (BDI). The study also examined the relationship between caregiver outcomes and patient-related clinical variables such as stroke severity and cognitive status.

Interventions

None listed

Sponsors

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Adult family caregivers (≥18 years old) providing care for patients with stroke who have lower urinary tract symptoms. Caregivers who have been providing care for at least 3 months. Caregivers who are able to read and understand the questionnaires. Caregivers who voluntarily agree to participate in the study.

Exclusion criteria

Caregivers with a previously diagnosed severe psychiatric disorder. Caregivers with cognitive impairment preventing completion of questionnaires. Caregivers who declined participation or provided incomplete questionnaire data.

Design outcomes

Primary

MeasureTime frameDescription
Caregiver burden measured by the Caregiver Strain Index (CSI)BaselineThe Caregiver Strain Index (CSI) is a validated questionnaire used to assess caregiver burden. It consists of 13 items evaluating strain related to caregiving activities. Higher scores indicate greater caregiver burden

Secondary

MeasureTime frameDescription
Sleep quality measured by the Pittsburgh Sleep Quality Index (PSQI)baselineThe Pittsburgh Sleep Quality Index (PSQI) is a validated instrument used to assess sleep quality and disturbances over the past month. Higher scores indicate poorer sleep quality
Depression measured by the Beck Depression Inventory (BDI)baselineThe Beck Depression Inventory (BDI) is a widely used self-report instrument that assesses depressive symptoms. Higher scores indicate greater depression severity.
Fatigue Severity Scale (FSS)baselineThe Fatigue Severity Scale (FSS) is a 9-item self-report questionnaire used to assess the severity and impact of fatigue on daily functioning. Higher scores indicate greater fatigue severity.
Caregiving Reactions QuestionnairebaselineThe Caregiving Reactions Questionnaire is a self-report instrument used to assess caregivers' emotional and psychological reactions associated with providing care to a family member with a chronic health condition.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORSEFA G ASLAN

gaziler physcial therapy and rehabilitation hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026